| Title of Invention | THERAPEUTIC POLYPEPTIDE CAPABLE OF ACTING AS ANTAGONIST OF TREM-1 PROTEIN. |
|---|---|
| Abstract | A pc ypeptide comprising one or more sequences derived from CDR2 or DR3 of a TREM- 1 protein, characterised by the ability to treal, ameliorate or lessen the symatoms of sepsis, 5 sept c shock or sepsis-IiKe conditions. |
| Full Text | BXL-P037/PCT 2. THERAPEUTIC PEPTIDES AND METHOD The present invention relates to the field of immunology. More particularly, the present invention relates to inflammation and the use of proteins and peptides containing certain sequences of the TREM-1 protein and their functional equivalents (referred to herein as TREM1-peptides) in the treatment of disease, for example, sepsis and septic shock. Sepsis constitutes a significant consumption of intensive care resources and remains an ever-present problem in the intensive care unit. It has been estimated that between 400 000 and 500 000 patients are so affected each year in both the USA and Europe. Morbidity and mortality have remained high despite improvements in both supportive and anti- microbial therapies. Mortality rates vary from 40% for uncomplicated sepsis to 80% in those suffering from septic shock and multi-organ dysfunction. The pathogenesis of the conditions is now becoming better understood. Greater understanding of the complex network of immune, inflammatory and haematological mediators may allow the development of rational and novel therapies. Following an infection, innate and cognitive immune responses develop in sequential phases that build-up in specificity and complexity, resulting ultimately in the clearance of infectious agents and restoration of homeostasis. The innate immune response serves as the first line of defence and is initiated upon activation of pattern recognition receptors, such as Toll - like receptors (TLRs) (1, 2), by various pathogen -associated microbial patterns (PAMPs) β). Activation of the TLRs triggers the release of large quantities of such cytokines as TNF -a and IL-1f5, which, in case of such massive infections as sepsis, can precipitate tissue injury and lethal shock (4, 5). Although antagonists of TNF -a and IL-1β appeared in this context as possibly interesting therapeutic agents of sepsis, they have unfortunately shown limited efficacy in clinical trials (6-8). This could be due to the fact that these cytokines are necessary for the clearance of infections, and that their removal would allow for fatal bacterial growth (9 -11). Another receptor involved in, inter alia, response to infection, t riggering receptor expressed on myeloid cells-1 (TREM -1) is a member of a recently discovered family of receptors, the TREM family, expressed on the surface of neutrophils and a subset of monocytes. TREM receptors activate myeloid cells via association with the adaptor molecule DAP12. Engagement of TREM -1 has been reported to trigger the synthesis of pro -inflammatory ' cytokines in the presence of microbial products. The triggering receptor expressed on myeloid cells (TREM) -1 is a recently discovered cell-surface molecule that has been identified both on human and murine polymorphonuclear neutrophils and mature monocytes (12). It belongs to the immunoglobulin superfamily and activates downstream signalling pathways with the help of an adapter protein called DAP12 (12 - 15). Bouchon and co -workers have shown that the expression of TREM-1 was greatly up- regulated on neutrophils and monocytes in the presence of such bacteria as Pseudomonas BXL-P037/PCT 3 aeruginosa or Staphytococcus aureus, both in cell culture and in tissue samples from patients with infection (16). In striking contrast, TREM-1 was not up- regulated in samples from patients with non-infectious inflammatory diseases such as psoriasis, ulcerative colitis or vasculitis caused by immune complexes (16). Moreover, when TREM-1 is bound to its ligand, there is a synergistic effect of LPS and an amplified synthesis of the pro- inflammatory cytokines TNF- a and GM-CSF, together with an inhibition of IL-10 production (17). In a murine model of LPS- induced septic shock, blockade of TREM -1 signalling protected the animals from death, further highlighting the crucial role of this molecule (13, 16). Recent studies demonstrate that TREM-1 plays a critical role in the inflammatory response to infection (see BOUCHON et al. (2000) J. Immunol. 164:4991 -4995). Expression of TREM-1 is increased on myeloid cells in response to both bacterial and fungal infections in humans. Similarly, in mice the induction of shock by lipopolysaccharide (LPS) is associated with increased expression of TREM -1. Further, treatment of mice with a soluble TREM -1/lg fusion protein, as a 'decoy' receptor, protects mice from death due to LPS or E.coii. US 6,420,526 entitled "186 Secreted Proteins" claims unspecified and unexemplified isolated fragments of TREM-1 containing at least 30 contiguous amino acids of human TREM-1. No biological data relating to such fragments are provided . As described in US2003165875A, fusion proteins between human lgG1 constant region and the extracellular domain of mouse TREM-1 or that of human TREM- 1 show an effect against endotoxemia in mice. The inventors have surprisingly found that certain peptides derived from the TREM -1 protein are capable of acting as antagonists of the TREM-1 protein and therefore have applications in the treatment of sepsis and septic shock. The Inventors further demonstrate that the same peptides also modulate in vivo the pro- inflammatory cascade triggered by infection, thus inhibiting hyper-responsiveness and death in an animal model of sepsis. Previously, the Inventors have identified a soluble form of TREM -1 (sTREM-1) and observed significant levels in serum samples from septic shock patients but not controls. As also described herein the Inventors have investigated its putative role in the modulation of inflammation during sepsis (see Gibot et al (2004) Ann. Intern. Med. 141(1):9-15 and Gibot et al. (2004) N. Engl. J. Med. 350(5):451 -8). As described herein the Inventors show that a soluble form of TREM-1 (sTREM -1) is released in the peripheral blood during infectious aggression in mouse. The Inventors also confirm monocytes as a major source of sTREM, and show that synthetic peptides mimicking a part of the extra-cellular domain of TREM-1 can modulate cytokine production by activated monocytes in vitro. The Inventors have observed that sTREM -1 is secreted by monocytes activated in vitro by LPS, as well as in the serum of animals involved in an experimental model of septic shock. BXL-P037/PCT 4 Both in vitro and in vivo, synthetic peptides mimicking a short highly conserved domain of sTREM-1 attenuate cytokine production by human monocytes and protect septic animals from hyper-responsiveness and death. These peptides are efficient not only in preventing but also in down-regulating the deleterious effects of pro -inflammatory cytokines. These data demonstrate that in vivo modulation of TREM -1 by TREM-1 peptides is a valuable therapeutic tool for the treatment of infection, for example sepsis or septic shock or for the treatment of sepsis-like conditions Accordingly, the present invention provides methods and compositions for the treatment of infectious disease, in particular, sepsis and septic shock or for the treatment of sepsis-like conditions As described herein, the Inventors have determined that several peptides of the extracellular portion of the TREM-1 protein (see Table 1), which incorporate sequences from "CDR2" and "CDR3" surprisingly have activity similar to previously described fusion proteins of lgG1 constant region and the extracellular domain of TREM-1 in models of sepsis. These peptides also have advantages over the protein particularly in terms of cost of manufacture. Thus, the invention provides polypeptides comprising one or more sequences derived from CDR2 or CDR3 of a TREM-1 protein. Preferably, said polypeptides comprise less than 30 contiguous amino acids of said TREM-1 protern. As shown in Table 1, examples of such peptides or polypeptides, contain or comprise for example 15-25 amino acid ("AA") peptides from the TREM-1 protein and contain or comprise all or part of a CDR domain β -6 AAs) of the receptor flanked by natural sequences from the protein that can vary in length so long as function of the CDR -like domain is not lost. Such peptides are derived from the TREM-1 receptor protein amino acid sequence for example, as shown in Table 2 (human) and Table 3 (mouse). Table 1 shows peptides derived from mouse TREM- 1 "mPX" (NCBI Reference Sequences (RefSeq) NP_067381) or human TREM-1 "hPX"" (NCBI Reference Sequences (RefSeq) NP_061113). Underlined amino acids span the human TREM -1 Complementarity Determining Regions (CDR), as described b y Radaev et al. 2003 Structure (Camb.) 11 (12), 1527-1535(2003). Table 2 shows the human TREM-1 amino acid sequence NP_061113. Underlined amino acids span the human TREM-1 Complementarity Determining Regions (CDR) 2 (RPSKNS; [SEQ ID NO:20]) and 3 (QPPKE [SEQ ID NO:21]), as described by Radaev et al. 2003 Structure (Camb.) 11 (12), 1527-1535(2003). Table 3 shows the mouse TREM-1 amino acid sequence NP_367381. Underlined amino acids span the mouse TREM-1 Complementarity Determining Regions (CDR) 2 (RPFT RP; [SEQ ID NO:22]) and 3 (HPPND; [SEQ ID NO:23]). BXL-P037/PCT 5 Table 1. Peptides including sequences from human and mouse TREM-1 CDR 2 and CDR 3 hCDR 2 mP1 (67-89) : [SEQ ID N0:3] LVVTQRPFTRPSEVHMGKFTLKH hP1 (67-89) : [SEQ ID NO:16] LACTERPSKNSHPVQVGRIILED hCDR 3 mP2 (114-136) : [SEQ ID NO:4] VIYHPPNDPVVLFHPVRLVVTKG mP4(103-123):[SEQ ID NO:6] LQVTDSGLYRCVIYHPPNDPV mP5(103-119) : [SEQ ID NO:7] LQVTDSGLYRCVIYHPP hP2 (114-136) : [SEQ ID NO:17] VIYQPPKEPHMLFDRIRLVVTKG hP4 (103-123) : [SEQ ID NO:16] LQVEDSGLYQCVIYQPPKEPH hP5 (103-119) : [SEQ ID NO:19] LQVEDSGLYQCVIYQPP Table 2 Human TREM-1 amino acid sequence NP_061113 1 MRKTRLWGLL WMLFVSELRA ATKLTEEKYE LKEGQTLDVK CDYTLEKFAS SQKAWQIIRD 61 GEMPKTLACT ERPSKNSHPV QVGRIILEDY HDHGLLRVRM VNLQVEDSGL YQCVIYQPPK 121 EPHMLFDRIR LWTKGFSGT PGSNENSTQN VYKIPPTTTK ALCPLYTSPR TVTQAPPKST 181 ADVSTPDSEI NLTNVTDIIR VPVFNIVILL AGGFLSKSLV FSVLFAVTLR SFVP [SEQ ID NO:1] Table 3 Mouse TREM-1 amino acid sequence NP_367381 1 MRKAGLWGLL CVFFVSEVKA AIVLEEERYD LVEGQTLTVK CPFNIMKYAN SQKAWQRLPD 61 GKEPLTLWT QRPFTRPSEV HMGKFTLKHD PSEAMLQVQM TDLQVTDSGL YRCVIYHPPN 121 DPWLFHPVR LWTKGSSDV PTPVIIPITR LTERPILITT KYSPSDTTTT RSLPKPTAW 181 SSPGLGVTII NGTDADSVST SSVTISVICG LLSKSLVFII LFIVTKRTFG [SEQ ID NO:2] Accordingly, the invention provides isolated or recombinantly prepared polypeptides or peptides comprising or consisting essentially of one or more sequences derived from CDR2 or CDR3 of a TREM-1 protein, or fragments, homologues, derivatives, fusion proteins or variants of such polypeptides, as defined herein, which are herein collectively referred to as "polypeptides or peptides of the invention" or "TREM-1 peptides or TREM-1 polypeptides", preferably such entities comprise less than 30 contiguous amino acids of a TREM -1 protein, for example as shown in Table 2 or Table 3. Generally where polypeptides or proteins of the invention or fragments, homologues, derivatives, or variants thereof are intended for use (for BXL-P037/PCT 6 example treatment) in a particular species, the sequences of CDR2 or CDR3 of a TREM -1 protein are chosen from the TREM-1 protein amino acid sequence of that species, or if the sequence is not known, an analogous species. For example, polypeptides or proteins of the invention for the treatment of human disease, in particular sepsis, septic shock or sepsis -like conditions, will comprise one or more sequences comprising ail or part of CDR2 or CDR3 from the human TREM-1 protein. Furthermore, the invention provides isolated polypeptides or proteins comprising an amino acid sequence that is at least about 60%, 70%, 75%, 80%, 85%, 90%, 95%, or 98% identical to the amino acid sequence of SEQ ID NO:20 , 21,22, 23 or fragments, homologues, derivatives, or variants thereof. The invention also provides isolated peptides, polypeptides or proteins comprising an amino acid sequence that comprises or consists of at least about 3, 4, 5, 6,7,8,9, 10, 11, 12,13, 14, 15, 16, 17, 18, 19,20,21 22, 23, 24, 25, 26 ,27 28 or 29 or more contiguous amino acids of a TREM-1 protein of which 3 or more contiguous amino acids are derived from the sequences of SEQ ID NO:20 , 21, 22 or 23 (in other words a sequence representing all, or part of CDR2 or CDR3 of a TREM-1 protein is present in the peptide, polypeptide or protein), or fragments, ho mologues, derivatives, or variants thereof. In preferred embodiments, such peptides, polypeptides or proteins, or fragments, homologues, derivatives or variants thereof have a biological activity of a TREM -1 full-length protein, such as antigenicity, immunogenicity, triggering of proinflammatory chemokines and cytokines, mobilization of cytosolic Ca2+, protein tyrosine-phosphoryiation, mediator release, and other activities readily assayable. Generally, such peptides, polypeptides or proteins or fragments, homologues, derivatives or variants thereof are capable of treating sepsis, septic shock or sepsis-like conditions, or are active in experimental models of sepsis, septic shock or sepsis-like conditions, for example by acting as antagonists of the activit y of the TREM-1 receptor. Such peptides, polypeptides or proteins or fragments, homologues, derivatives or variants thereof are characterised by the ability to treat, ameliorate, or lessen the symptoms of sepsis, septic shock or sepsis-like conditions. In particular, the invention provides, a TREM-1 polypeptide having activity against sepsis, septic shock or sepsis-like conditions which consists of (i) a contiguous sequence of 5 to 29, for example 15-25, amino acids corresponding to the native TREM -1 protein sequence which includes at least 3 amino acids from the CDR2 or CDR3 sequences; or (ii) such a sequence in which one or more amino acids are substituted conservatively with another amino acid provided, however that at least 3 amino acids from the CDR2 or CDR3 sequences are not substituted; or (iii) a sequence of (i) or (ii) linked at one or both of its N and C termini to a heterologous polypeptide. For example, in a polypeptide wherein the native TREM-1 protein sequence is the human sequence identified a s [SEQ ID NO: 1], the CDR2 and CDR3 sequences are RPSKNS and QPPKE respectively. In such poiypeptides, the at least 3 amino BXL-P037/PCT 7 acids from the CDR2 or CDR3 sequences can be QPP, PPK, PKE, RPS, PSK, SKN or KNS. Such polypeptides may comprise the sequence QPPK, QPPKE or RPSKNS. For example, in a polypeptide wherein the native TREM -1 protein sequence is the mouse sequence identified as [SEQ ID NO: 2] the CDR2 and CDR3 sequences are RPFTRP and HPPND respectively. In such polypeptides, the at least 3 amino acids from the CDR2 or CDR3 sequences can be HPP, PPN, PND, RPF, PFT, FTR or TRP. Such polypeptides may comprise the sequences HPP, HPPN, HPPND or RPFTRP. In certain embodiments, the polypeptide of the invention is or comprises SEQ ID No. 7 which is disclosed in Gibot et al (2004) J Exp Med 200, 1419-1426.. In certain embodiments the polypeptide of the invention neither is nor comprises SEQ ID No. 7. In certain embodiments the polypeptide of the invention is or comprises a sequence selected from SEQ ID Nos. 3, 4 and 6. In certain embodiments the polypeptide of the invention is or comprises a sequence selected from SEQ ID Nos. 16, 17, 18 and 19. In certain embodiments the polypeptide of the invention is or comprises a sequence derived from CDR2. In certain embodiments the polypeptide of the invention is or comprises a sequence derived from CDR3. The polypeptides or peptides of the invention are provided for use in therapy, in particular in the treatment of sepsis, septic shock and sepsis-like conditions, and for us e in the manufacture of a medicament for the treatment of sepsis , septic shock and sepsis-like conditions. Further provided are compositions and pharmaceutical compositions containing polypeptides or peptides of the invention and methods of treatment of sepsis , septic shock and sepsis-like conditions using polypeptides or peptides of the invention. In addition the pofypeptides or peptides of the invention are provided for use in therapy to restore haemodynamic parameters in sepsis, septic shock and sepsis-like conditions and for use in the manufacture of a medicament for the treatment of aberrant haemodynamic parameters in sepsis, septic shock and sepsis-like conditions. The term "triggering receptor expressed on myeloid cells" or "TREM" refers to a group of activating receptors which are selectively expressed on different types of myeloid cells, such as mast cells, monocytes, macrophages, dendritic cells (DCs), and neutrophils, and may have a predominant role in immune and inflammatory responses. TREMs ar e primarily transmembrane glycoproteins with a Ig-type fold in their extracellular domain and, hence, belong to the Ig-SF. These receptors contain a short intracellular domain, but lack docking motifs for signaling mediators and require adapter proteins, such as DAP12, for cell activation. BXL-P037/PCT 8 The term "myeloid cells" as used herein refers to a series of bone marrow- derived cell lineages including granulocytes (neutrophils, eosinophils, and basophils), monocytes, macrophages, and mast cells. Furthermore, peripheral blood dendritic cells of myeloid origin, and dendritic cells and macrophages derived in vitro from monocytes in the presence of appropriate culture conditions, are also included. The term "sepsis, septic shock" or "sepsis or septic shock" as defined herein, refers to sub-groups of systemic inflammatory response syndrome (SIRS). The term "sepsis" is generally reserved for SIRS when infection is suspected or proven. A pattern of physiological variables have been shown in critically ill patients in re sponse to a range of insults including; trauma, burns, pancreatitis and infection. These include inflammatory responses, leucocytosis or severe leucopaenia, hyperthermia or hypothermia, tachycardia and tachypnoea and have been collectively termed the systemic inflammatory response syndrome (SIRS). This definition emphasises the importance of the inflammatory process in these conditions regardless of the presence of infection. Sepsis is further stratified into severe sepsis when there is evidence of organ hypoperfusion, made evident by signs of organ dysfunction such as hypoxaemia, oliguria, lactic acidosis or altered cerebral function. "Septic shock" is severe sepsis usually complicated by hypotension, defined in humans as systolic blood pressure less than 90 mmHg despite adequate fluid resuscitation. Sepsis and SIRS may be complicated by the failure of two or more organs, termed multiple organ failure (MOF), due to disordered organ perfusion and oxygenation. In addition to systemic effects of infection, a sy stemic inflammatory response may occur in severe inflammatory conditions such as pancreatitis and burns. The appearance of signs of an inflammatory response is less well defined following traumatic insults. In the intensive care unit, gram -negative bacteria are implicated in 50 to 60% of sepsis cases with gram-positive bacteria accounting for a further 35 to 40% of cases. The remainder of cases are due to the less common causes of fungi, viruses and protozoa. The term "sepsis-like conditions" as used herein refers to those states in which a patient presents with symptoms similar to sepsis or septic shock but where an infectious agent is not the primary or initial cause of a similar cascade of inflammatory mediators and/or change in haemodynamic parameters a s seen in cases of sepsis, for example in patients with acute or chronic liver failure (see Wasmuth HE, et al. J Hepatol. 2005 Feb;42(2):195 -201), in cases of post-resuscitation disease after cardiac arrest (see Adrie C et al. Curr Opin Crit Care. 2004 Jun;10β):208-12) in the treatment of sepsis-like symptoms after cancer chemotherapy (see Tsuji E et al. Int J Cancer. 2003 Nov 1;107(2):303-8) in patients undergoing hyperthermic isolated limb perfusion with recombinant TNF- alpha or similar treatments (see Zwaveling JH et al. Crit Care Med. 1996 May;24(5):765 -70) or sepsis-like illness in neonates (see Griffin MP et al. Pediatr Res. 2003 Jun;53(6):920 -6). BXL-P037/PCT 9 The term "activity against sepsis, septic shock or sepsis-like conditions" as used herein refers to the capability of a molecule, for example a peptide, polypeptide or engineered antibody, to treat sepsis, septic shock or sepsis -like conditions, or be active in experimental models of sepsis, septic shock or sepsis-like conditions, for example by acting as an antagonist of the activity of the TREM-1 receptor. Typically the indication for polypeptides of the invention is sepsis or septic-shock. The term "substantial sequence identity", when used in connection with peptides/amino acid sequences, refers to peptides/amino acid sequences which are substantially identical to or similar in sequence, giving rise to a homology in conformation and thus to similar biological activity. The term is not intended to imply a common evolution of the sequences. Typically, peptides/amino acid sequences having "substantial sequence identity" are sequences that are at least 50%, more preferably at least 80%, identical in sequence, at least over any regions known to be involved in the desired activity. Most preferably, no more than five residues, other than at the termini, are different. Preferably, the divergence in sequence, at least in the aforementioned regions, is in the form of "conservative modifications" To determine the percent sequence identity of two peptides/ amin o acid sequences or of two nucleic acid sequences, the sequences are aligned for optimal comparison purposes ( e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non -homologous sequences can be disregarded for comparison purposes). For example, the length of a reference sequence aligned for comparison purposes is at least 30%, preferably at least 40%, more preferably at least 50%, even more preferably at least 60%, and even more preferably at least 70%, 80%, or 90% of the length of the reference sequence (e.g., when aligning a second sequence to the first amino acid sequence which has for example 100 amino acid residues, at least 30, preferably at least 40, more preferably at least 50, even more preferably at least 60, and even more preferably at least 70, 80 or 90 amino acid residues are aligned). The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid "identity" is equivalent to amino acid or nucleic acid "homology"). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introd uced for optimal alignment of the two sequences. The comparison of sequences and determination of percent identity between two sequences can be accomplished using a mathematical algorithm. In one embodiment, the percent identity between two amino acid se quences is determined using the Needleman and Wunsch ( J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the BXL-P037/PCT 10 GCG software package (available at http://www.gcg.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4, and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package {available at http://www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80, and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the alg orithm of E. Meyers and W. Miiier (CABIOS, 4:11 -17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12, and a gap penalty of 4. The nucleic acid and protein sequences of the present invention can further be used as a "query sequence" to perform a search against public databases to identify, for example, other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et a/. (1990) J. Mol. Biol. 215:403- 10. BLAST nucleotide searches can be performed with the NBLAST program, score = 100, wordlength = 12 to obtain nucleotide sequences homologous to NIP2b, NlP2cL, and NIP2cS nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST program, score = 50, wordlength = 3 to obtain amino acid sequences homologous to NIP2b, NIP2cL, and NIP2cS protein molecules of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul etal., (1997) Nucleic Acids Res. 25(17):3389-3402. When utilizing BLAST and Gapped BLAST programs, the default parameters of the respective programs ( e.g., XBLAST and NBLAST) can be used. See http://www.ncbi.nlm.nih.gov. The terms "protein" and "polypeptide" are used interchangeably herein. The term "peptide" is used herein to refer to a chain of two or more amino acids or amino acid analogues (including non-naturally occurring amino acids), with adjacent amino acids joined by peptide (- NHCO-) bonds. Thus, the peptides of the invention include oligopeptides, polypeptides, proteins, mimetopes and peptidomimetics. Methods for preparing mimetopes and peptidomimetics are known in the art. The terms "mimetope" and "peptidomimetic" are used interchangeably herein. A "mimetope" of a' compound X refers to a compound in which chemical structures of X necessary for functional activity of X have been replaced with other chemical structures which mimic the conformation of X. Examples of peptidomimetics include peptidic compounds in which the peptide backbone is substituted with one or more benzodiazepine molecules (see e.g., James, G.L. et ai. (1993) Science 260:1937-1942) and "retro-inverso" peptides (see U.S. Patent No. 4,522,752 to Sisto). The terms "mimetope" and "peptidomimetic" also refer to a moiety, other than a naturally occurring amino acid, that conformationally and functionally serves as a substitute for a particular amino acid in a p eptide-containing compound without adversely BXL-P037/PCT 11 interfering to a significant extent with the function of the peptide. Examples of amino acid mimetics include D-amino acids. Peptides substituted with one or more D- amino acids may be made using well known peptide synthesis procedures. Additional substitutions include amino acid analogues having variant side chains with functional groups, for example, b -cyanoalanine, canavanine, djenkolic acid, norleucine, 3-phosphoserine, homoserine, dihydroxyphenylalanine, 5-hydroxytryptophan, 1 -methylhistidine, or 3-methylhistidine As used herein an "analogue" of a compound X refers to a compound which retains chemical structures of X necessary for functional activity of X, yet which also contains certain chemical structures which differ from X. An example of an analogue of a naturally -occurring peptide is a peptide which includes one or more non-naturally-occurring amino acids. The term "analogue" is also intended to include modified mimetopes and/or peptidomimetics, modi fied peptides and polypeptides, and allelic variants of peptides and polypeptides. Analogues of a peptide will therefore produce a peptide analogue that is substantially homologous or, in other words, has substantial sequence identity to the original peptide. The term "amino acid" includes its art recognized meaning and broadly encompasses compounds of formula I: Preferred amino acids include the naturally occu rring amino acids, as well as synthetic derivatives, and amino acids derived from proteins, e.g., proteins such as casein, i.e. , casamino acids, or enzymatic or chemical digests of, e.g., yeast, an animal product, e.g., a meat digest, or a plant product, e.g., soy protein, cottonseed protein, or a corn steep liquor (see, e.g., Traders' Guide to Fermentation Media, Traders Protein, Memphis, TN (1988), Biotechnology: A Textbook of Industrial Microbiology, Sinauer Associates, Sunderland, MA (1989), and Product Data Sheet for Corn Steep Liquor, Grain Processing Corp., IO). The term "naturally occurring amino acid" includes any of the 20 amino acid residues which commonly comprise most polypeptides in living systems, rarer amino acids found in fibrous proteins (e.g., 4-hydorxyproline, 5-hydroxyIysine, -N-methyliysine, 3-methylhistidine, desmosine, isodesmosine), and naturally occurring amino acids not found in proteins (e.g. , aminobutryic acid, homocysteine, homoserine, citrulline, ornithine, canavanine, d jenkolic acid, and -cyanoalanine). The term "side chain of a naturally occurring amino acid" is intended to include the side chain of any of the naturally occurring amino acids, as represented by R in formula 1. One skilled in the art will understand that the structure of formula 1 is intended to encompass amino BXL-P037/PCT 12 acids such as praline where the side chain is a cyclic or heterocyclic structure (e.g. , in praline R group and the amino group form a five -membered heterocyclic ring. The term "homologue,".a s used herein refers to any member of a series of peptides or poiypeptides having a common biological activity, including antigenicity/immunogenicity and inflammation regulatory activity, and/or structural domain and having sufficient amino acid as defined herein. Such homologues can be from either the same or different species of animals. The term "variant" as used herein refers either to a naturally occurring allelic variation of a given peptide or a recombinantly prepared variation of a given peptide or protein in which one or more amino acid residues have been modified by amino acid substitution, addition, or deletion. The term "derivative" as used herein refers to a variation of given peptide or protein that are otherwise modified, i.e., by covalent a ttachment of any type of molecule, preferably having bioactivity, to the peptide or protein, including non -naturally occurring amino acids. Preferably, such homologues, variants and derivatives are capable of treating of sepsis, septic shock or sepsis-like conditions, or are active in experimental models of sepsis, septic shock or sepsis-like conditions, for example by acting as antagonists of the activity of the TREM-1 receptor. An "isolated" or "purified" peptide or protein is substantially free of cell ular material or other contaminating proteins from the cell or tissue source from which the protein is derived, or substantially free of chemical precursors or other chemicals when chemically synthesized. The language "substantially free of cellular material" includes preparations of a polypeptide/protein in which the polypeptide/protein is separated from cellular components of the cells from which it is isolated or recombinantly produced. Thus, a polypeptide/protein that is substantially free of cellular material includes preparations of the polypeptide/protein having less than about 30%, 20%, 10%, 5%, 2.5%, or 1 %, (by dry weight) of contaminating protein. When the polypeptide/protein is recombinantly produced, it is also preferably substantially free of culture medium, i.e., culture medium represents less than about 20%, 10%, or 5% of the volume of the protein preparation. When poiypeptide/protein is produced by chemical synthesis, it is preferably substantially free of chemical precursors or other chemicals, i.e., it is separated from chemical precursors or other chemicals which are involved in the synthesis of the protein. Accordingly, such preparations of the polypeptide/protein have less than about 30%, 20%, 10%, 5% (by dry weight) of chemical precu rsors or compounds other than polypeptide/protein fragment of interest. In a preferred embodiment of the present invention, polypeptides/proteins are isolated or purified. In addition to the poiypeptides described above, poiypeptides of the invention also encompass those poiypeptides having a common biological activity and/or structural domain and having sufficient amino acid identity (homologues) as defined herein. These homologues BXL-P037/PCT 13 can be from either the same or different species of animal, preferably from mammals, more preferably from rodents, such as mouse and rat, and most preferably from human. Preferably, they exhibit at least one structural and/or functional feature of TREM -1, and are preferably, capable of treating sepsis, septic shock or sepsis -like conditions, for example by acting as antagonists of the activity of the TREM -1 receptor. Such modifications include amino acid substitution, deletion, and/or insertion. Amino acid modifications can be made by any method known in the art and various methods are available to and routine for those skilled in the art. Additionally, in making amino acid substitutions, generally the amino acid residue to be substituted can be a conservative amino acid substitution (i.e. "substituted conservatively"), for example, a polar residue is substituted with a polar residue, a hydrophilic residue with a hydrophilic residue, hydrophobic residue with a hydrophobic residue, a positively charged residue with a positively charged residue, or a negatively charged residue w ith a negatively charged residue. Moreover, generally, the amino acid residue to be modified is not highly or completely conserved across species and/or is critical to maintain the biological activities of the peptide and/or the protein it derives from. Peptides of the invention may be directly synthesised in any convenient way. Generally the reactive groups present (for example amino, thiol and/or carboxyl) will be protected during overall synthesis. A proportion of the peptides of the invention, i. e. th ose wherein the comprised amino acids are genetically coded amino acids, will be capable of being expressed in prokaryotic and eukaryotic hosts by expression systems well known to the man skilled in the art. Methods for the isolation and purification of e. g. microbially expressed peptides are also well known. Polynucleotides which encode these peptides of the invention constitute further aspects of the present invention. As used herein, "polynucleotide" refers to a polymer of deoxyribonucleotides or ribonucleotides, in the form of a separate fragment or as a component of a larger construct, e. g. an expression vector such as a plasmid. Polynucleotide sequences of the invention include DNA, RNA and cDNA sequences. Due to the degeneracy of the genetic code, of course more than one polynucleotide is capable of encoding a particular peptide according to the invention. When a bacterial host is chosen for expression of a peptide, it may be necessary to take steps to protect the host from the expressed anti -bacterial peptide. Such techniques are known in the art and include the use of a bacterial strain which is resistant to the particular peptide being expressed or the expression of a fusion peptide with sections at one or both ends which disable the antibiotic ac tivity of the peptide according to the invention. In the latter case, the peptide can be cleaved after harvesting to produce the active peptide. If the peptide incorporates a chemical modification then the activity/stability of the expressed peptide may be low, and is only modulated by post-synthetic chemical modification Furthermore, the invention also encompasses derivatives of the polypeptides of the invention. For example, but not by way of limitation, derivatives may include peptides or BXL-P037/PCT 14 proteins that have been modified, e.g., by glycosylation, acetylation, pegylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, linkage to a cellular ligand or other protein, etc. Any of numerous chemical modifications may be carried out by known techniques, including, but not limited to, specific chemical cleavage, acetylation, formyiation, etc. Additionally, the derivative may contain one or more non-classical amino acids. Those skilled in the art will be aware of various methods for modifying peptides to increase potency, prolong activity and/or increase half-life. In one example (WO0210195) the modification is made via coupling through an amide bond with at least one conformationally rigid substituent, either at the N- terminal of the peptide, the C- terminal of the peptide, or on a free amino or carboxyl group along the peptide chain. Other examples of peptide modifications with similar effects are described, for example, in WO2004029081, WO03086444, WO03049684, WO0145746, WO0103723 and WO9101743. The invention further provides antibodies that comprise a peptide or polypeptide of the invention or that mimic the activity of peptides or polypeptides of the invention. Such antibodies include, but are not limited to: polyclonal, monoclonal, bi-specific, multi-specific, human, humanized, chimeric antibodies, single chain antibodies, Fab fragments, F(ab')2 fragments, disulfide-linked Fvs, and fragments containing either a Vl_ or VH domain or even a complementary determining region (CDR) that specifically binds to a polypeptide of the invention. In another embodiment, antibodies can also be generated using various phage display methods known in the art. Techniques to recombinantly produce Fab, Fab' and F(ab')2 fragments can aiso be employed using methods known in the art such as those disclosed in PCT publication WO 92/22324; Mullinax, et al., BioTechniques, 12(6):864 -869, 1992; and Sawai, et al, 1995, AJRI 34:26-34; and Better, etal., 1988, Science 240:1041-1043 ( each of which is incorporated by reference in its entirety). Examples of techniques that can be used to produce single-chain Fvs and antibodies include those described in U.S. Patent Nos. 4,946,778 and 5,258,498; Huston, et al., 1991, Methods in Enzymology 203:46-88; Shu, et al., 1993, Proc. Natl. Acad. Sci. USA 90:7995-7999; and Skerra, et al., 1988, Science 240:1038-1040. For some uses, including in vivo use of antibodies in humans and in vitro detection assays, it may be preferable to use chimeric, humanized, or human antibodies. A chimeric antibody is a molecule in which different portions of the antibody are derived from different animal species, such as antibodies having a variable region derived from a murine monoclonal antibody and a constant region derived from a human immunoglobulin. Methods for producing chimeric antibodies are known in the art. See, e.g., Morrison, 1985, Science 229:1202; Oi, etal., 1986, BioTechniques 4:214; Gillies, et al., 1989, J. Immunol. Methods 125:191 -202; U.S. Patent Nos. 5,807,715; 4,816,567; and 4,816,397; which are incorporated herein by reference in their entireties. Humanized antibodies are antibody molecules from non-human species that bind the desired antigen having one or more complementarity determining reg ions (CDRs) from the non- BXL-P037/PCT 15 human species and framework regions from a human immunoglobulin molecule or in the case of the present invention, one or more CDRs derived from a TREM-1 protein. As known in the art, framework residues in the human framework regions can be substituted with the corresponding residue from the CDR donor antibody to alter, preferably improve, antigen binding. These framework substitutions are identified by methods well known in the art, e.g., by modelling of the interactions of the CD R and framework residues to identify framework residues important for antigen binding and sequence comparison to identify unusual framework residues at particular positions. See, e.g., Queen, et al., U.S. Patent No. 5,585,089; Riechmann, et a!., 1988, Nature 332:323, 1988, which are incorporated herein by reference in their entireties. Antibodies can be humanized using a variety of techniques known in the art including, for example, CDR-grafting (EP 239,400; PCT publication WO 91/09967; U.S. Patent Nos. 5,225,539; 5,530,101 and 5,585,089), veneering or resurfacing (EP 592,106; EP 519,596; Padlan, 1991, Molecular Immunology, 28(4/5):489 -498; Studnicka, et al., 1994, Protein Engineering, 7(6):805-814; Roguska, et al., 1994, Proc Natl. Acad. Sci. USA 91:969 -973, and chain shuffling (U.S. Patent No. 5,565,332), all of which are hereby incorporated by reference in their entireties. Completely human antibodies are particularly desirable for therapeutic treatment of human patients. Human antibodies can be made b y a variety of methods known in the art including phage display methods described above using antibody libraries derived from human immunoglobulin sequences. See U.S. Patent Nos. 4,444,887 and 4,716,111; and PCT publications WO 98/46645; WO 98/50433; WO 98/24893; WO 98/16654; WO 96/34096; WO 96/33735; and WO 91/10741, each of which is incorporated herein by reference in its entirety. Human antibodies can also be produced using transgenic mice (see Lonberg and Huszar (1995), int. Rev. Immunol. 13:65-93). For a detailed discussion of this technology for producing human antibodies and human monoclonal antibodies and protocols for producing such antibodies, see, e.g., PCT publications WO 98/24893; WO 92/01047; WO 96/34096; WO 96/33735; European Patent No. 0 598 877; U.S. Patent Nos. 5,413,923; 5,625,126; 5,633,425; 5,569,825; 5,661,016; 5,545,806; 5,814,318; 5,885,793; 5,916,771; and 5,939,598; which are incorporated by reference herein in their entireties. In addition, companies such as Abgenix, Inc. (Freemont, CA), Medarex (NJ) and Genpharm (San Jose, CA) can be engaged to provide human antibodies directed against a selected antigen using technology similar to that described above. Completely human antibodies which recognize a selected epitope can be generated using a technique referred to as "guided selection." In this approach a selected non -human monoclonal antibody, e.g., a mouse antibody, is used to guide the selection of a completely human antibody recognizing the same epitope. (Jespers et al., 1988, Bio/technology 12:899- 903). Antibodies fused or conjugated to heterologous polypeptides may be used in in vitro immunoassays and in purification methods (e.g., affinity chromatography) well known in the art. BXL-P037/PCT 16 See, e.g., PCT publication Number WO 93/21232; EP 439,095; Naramura, et al., 1994, Immunol. Lett. 39:91-99; U.S. Patent 5,474,981; Gillies, et al., 1992 Proc. Natl. Acad. Sci. USA 89:1428-1432; and Fell, et al., 1991, J. immunol. 146:2446-2452, which are incorporated herein by reference in their entireties. In another aspect, the present invention provides methods for identifying a compound or ligand that binds to or modulates the activity of a polypeptide of the invention. Such a method comprises measuring a biological activity of the poiypeptide in the presence or absence of a test compound and identifying test compounds that alter (increase or decrease) the biological activity of the polypeptide. in one embodiment, the invention provides a fusion protein comprising a bioactive molecule and one o r more domains of a polypeptide of the invention or fragment thereof. In particular, the present invention provides fusion proteins comprising a bioactive molecule recombinantly fused or chemically conjugated (including both covalent and non -covalent conjugations) to one or more domains of a polypeptide of the invention or fragments thereof. The present invention further encompasses fusion proteins in which the polypeptides of the invention or fragments thereof, are recombinantly fused or chemically conju gated (including both covalent and non-covalent conjugations) to heterologous polypeptides (i.e., an unrelated polypeptide or portion thereof, preferably at least 10, at least 20, at least 30, at least 40, at least 50, at least 60, at least 70, at least 80, at least 90 or at least 100 amino acids of the polypeptide) to generate fusion proteins. The fusion does not necessarily need to be direct, but may occur through linker sequences. In one example, a fusion protein in which a polypeptide of the invention or a fragment thereof can be fused to sequences derived from various types of immunoglobulins. For example, a polypeptide of the invention can be fused to a constant region (e.g., hinge, CH2, and CH3 domains) of human lgG1 or IgM molecule, (for example, as described by Hudson & Souriauso (2003) Nature Medicine 9(1):129- 134) so as to make the fused polypeptides or fragments thereof more soluble and stable in vivo . The short half-life of antibody fragments can also be extended by 'pegylation', that is, a fusion to polyethylene glycol (see Leong, S.R. et al. (2001) Cytokine 16:106-119). In one example of such fusions, described in WO0183525, Fc domains are fused with biologically active peptides. A pharmacologically active compound is produced by covalently linking an Fc domain to at least one amino acid of a selected peptide. Linkage to the vehicle increases the half-life of the peptide, which otherwise could be quickly degraded in vivo Alternatively, non-classical alternative protein scaffolds (for exa mple see Nygren & Skerra (2004) J Immunol Methods 290(1 -2):3-28 or WO03049684) can be used to incorporate, and replicate the properties of, the peptides of the invention, for example by inserting peptide sequences derived from TREM -1 CDR2 or CDR3 into a protein framework to support BXL-P037/PCT 17- conformationally variable loops having structural/functional similarities to CDR2 or CDR3 in a fixed spatial arrangement Such fusion proteins or scaffold based proteins can be used as an immunogen for the production of specific antibodies which recognize the polypeptides of the invention or fragments thereof. In another preferred embodiment, such fusion proteins or scaffold based proteins can be administered to a subject so as to inhibit interactions between a ligand and its receptors in vivo. Such inhibition of the interaction will block or suppress certain cellular responses involved in sepsis and septic shock. in one aspect, the fusion protein comprises a polypeptide of the invention which is fused to a heterofogous signa I sequence at its N-terminus. Various signal sequences are commerciaily available. For example, the secretory sequences of melittin and human placental alkaline phosphatase (Stratagene; La Jolla, CA) are available as eukaryotic heterologous signal sequences. As examples of prokaryotic heterologous signal sequences, the phoA secretory signal (Sambrook, et al., supra; and Current Protocols in Molecular Biology, 1992, Ausubel, et al., eds., John Wiley & Sons) and the protein A secretory signal (Pharmacia Biotech; Piscataway, NJ) can be listed. Another example is the gp67 secretory sequence of the baculovirus envelope protein (Current Protocols in Molecular Biology, 1992, Ausubel, et al., eds., John Wiley & Sons). In another embodiment, a poiypeptide of the invention can be fused to tag sequences, e.g., a hexa-histidine peptide, such as the tag provided in a pQE vector (QIAGEN, Inc., 9259 Eton Avenue, Chatsworth, CA, 91311), among others, many of which are commercially available. As described in Gentz, et al., 1989, Proc. Natl. Acad. Sci. USA 86:821-824, for instance, hexa-histidine provides for convenient purification of the fusion protein. Other examples of peptide tags are the hemagglutinin "HA" tag, which corresponds to an epitope derived from the influenza hemagglutinin protein (Wilson, et al., 1984, Cell 37:767) and the "flag" tag (Knappik, et al., 1994, Biotechniques 17(4):754-761). These tags are especially useful for purification of recombinantly produced polypeptides of the invention. Fusion proteins can be produced by standard recombinant DNA techniques or by protein synthetic techniques, e.g., by use of a peptide synthesizer. For example, a nucleic acid molecule encoding a fusion protein can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and reamplified to g enerate a chimeric gene sequence (see, e.g., Current Protocols in Molecular Biology, 1992, Ausubel, et al., eds., John Wiley & Sons). The nucleotide sequence coding for a fusion protein can be inserted into an appropriate expression vector, i.e., a vector which contains the necessary elements for the transcription and translation of the inserted protein -coding sequence. Various BXL-P037/PCT 18 host-vector systems and selection systems are known. In a specific embodiment, the expression of a fusion protein is regulated by a constitutive promoter. In another embodiment, the expression of a fusion protein is regulated by an inducible promoter. In accordance with these embodiments, the promoter may be a tissue -specific promoter. Expression vectors containing inserts of a gene encoding a fusion protein can be identified by three general approaches: (a) nucleic acid hybridization, (b) presence or absence of "marker" gene functions, and (c) expression of inserted sequences. In the first approach, the presence of a gene encoding a fusion protein in an expression vector can be detected by nucleic acid hybridization using probes comprising sequences that are homologous to an inserted gene encoding the fusion protein. In the second approach, the recombinant vector/host system can be identified and selected based upon the presence or absence of certain "marker" gene functions (e.g., thymidine kinase activity, resistance to antibiotics, transformation phenotype, occlusion body formation in baculovirus, etc.) caused by the insertion of a nucleotide sequence encoding a fusion protein in the vector. For example, if the nucleotide sequence encoding the fusion protein is inserted within the marker gene sequence of the vector, recombinants containing the gene encoding the fusion protein i nsert can be identified by the absence of the marker gene function. In the third approach, recombinant expression vectors can be identified by assaying the gene product (i.e., fusion protein) expressed by the recombinant. Such assays can be based, for example, on the physical or functional properties of the fusion protein in in vitro assay systems, e.g., binding with anti-fusion protein antibody. For long- term, high-yield production of recombinant proteins, stable expression is preferred. For example, cell lines which stably express the fusion protein may be engineered. Rather than using expression vectors which contain viral origins of replication, host cells can be transformed with DNA controlled by appropriate expression control elements (e.g., promo ter, enhancer, sequences, transcription terminators, polyadenylation sites, etc.), and a selectable marker. Following the introduction of the foreign DNA, engineered cells may be allowed to grow for 1 -2 days in an enriched medium, and then are switched to a selective medium. The selectable marker in the recombinant plasmid confers resistance to the selection and allows cells to stably integrate the plasmid into their chromosomes and grow to form foci which in turn can be cloned and expanded into ceil lines. This method may advantageously be used to engineer cell lines that express the differentially expressed or pathway gene protein. Such engineered cell lines may be particularly useful in screening and evaluation of compounds that affect the endogenous activity of the differentially expressed or pathway gene protein. Once a fusion protein of the invention has been produced by recombinant expression, it may be purified by any method known in the art for purification of a protein, for example, by chromatography (e.g., ion exchange, affinity, particularly by affinity for the specific antibody, and sizing column chromatography), BXL-P037/PCT 19 centrifugation, differential solubility, or by any other standard technique for the purification of proteins. The present invention also provides methods for treating a subject suffering from sepsis, septic shock or a sepsis-like condition by administering a peptide or polypeptide of the invention. In another embodiment, the modulator may be an antibody which mimics the activity of a polypeptide of the invention. In particular, the invention provides a method of treating or ameliorating sepsis, septic shock or a sepsis-like condition in a subject, comprising: administering a therapeutically effective amount of a peptide or polypeptid e of any one of the preceding claims to a subject. In such methods, the peptide or polypeptide administered can have substantial sequence identity to sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19, is SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19, or an active fragment, analogue or derivative of SEQ ID NOS: 3,4, 6, 7, 16, 17, 18 or 19 or has at least about 80% sequence identity to SEQ ID NOS: 3, 4, 6,7, 16, 17, 18 or 19 In one aspect, the invention provides a method for preventing sepsis, septic shock or sepsis-like conditions, by administering to the subject a peptide or polypeptide of the invention. Subjects at risk of sepsis or septic shock can be identified by, for example, any diagnostic or prognostic assays as known in the art {for particularly suitable methods of diagnosis, see WO2004081233, Gibot et al. (2004) Ann Intern Med. 141(1):9-15 and Gibot et al. (2004) N Engl J Med. 350(5):451 -8. The prophylactic agents described herein, for example, can be used to treat a subject at risk of developing disorders such as those previously discussed. The methods of the invention are applicable to mammals, for example humans, non human primates, sheep, pigs, cows, horses, goats, dogs, cats and rodents, such as mouse and rat. Generally, the methods of the invention are to be used with human subjects. Furthermore, the invention provides a pharmaceutical composition comprising a polypeptide of the present invention or an antibody or fragments thereof that mimics a polypeptide of the invention. The peptides, polypeptides and antibodies (also referred to herein as "active compounds") of the invention can be incorporated into pharmaceutical compositions suitable for administration. Such compositions typically comprise the peptide, protein, or antibody and a pharmaceutically acceptable carrier. As used herein the language " pharmaceutically acceptable diluent, carrier or excipient" is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption d elaying agents, and the like, compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the compositions is contemplated. Supplementary active compounds can also be incorporated into the compositions. BXL-P037/PCT 20 The invention includes methods for preparing pharmaceutical compositions containing a peptide or polypeptide of the invention. Such compositions can further include additional active agents. Thus, the invention further includes methods for preparing a pharmaceutical composition by formulating a pharmaceutically acceptable carrier with a peptide or polypeptide of the invention and one or more additional active compounds. A pharmaceutical composition of the invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, transdermal (topical), transmucosal, intra-articular, intra peritoneal, and intrapleural, as well as oral, inhalation, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous applicat ion can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parab ens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic. Pharmaceutical compositions suitable for injectab le use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. For intravenous administration, suitable carriers include physiological sa line, bacteriostatic water, Cremophor EL ™ (BASF; Parsippany,' NJ) or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy injectability with a syringe exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyetheylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many ca ses, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin. BXL-P037/PCT 21 Sterile injectable solutions can be prepared by incorporating the active compound (e.g., a polypeptide or antibody) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the require d other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectabie solutions, the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof. Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient, such as starch or lactose; a disintegrating agent, such as alginic acid, Primogel, or com starch; a lubricant, such as magnesium stearate or Sterotes; a glidant, such as colloidal silicon dioxide; a sweetening agent, such as sucrose or saccharin; or a flavoring agent, such as peppermint, methyl salicylate, or orange flavoring. For administration by inhalation, the compounds are delivered in the form of an aerosol spray from a pressurized container or dispenser which contains a suitable propellant, e.g., a gas such as carbon dioxide, or a nebulizer. Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration , the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art. The compounds can also be prepared in the form of suppositories (e.g., with conventional suppository bases such as cocoa butter and other glycerid es) or retention enemas for rectal delivery. In one embodiment, the active compounds are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microe ncapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will BXL-P037/PCT 22 be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Corporation and Nova Pharmaceuticals, Inc. Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Patent No. 4,522,811. It is especially advantageous to formulate oral or parenteral co mpositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of individuals. As defined herein, a therapeutically effective amount of protein or polypeptide (i.e., an effective dosage) ranges from about 0.001 to 30 mg/kg body weight, preferably about 0.01 to 25 mg/kg body weight, more preferably about 0.1 to 20 mg/kg body weight, and even more preferably about 1 to 10 mg/kg, 2 to 9 mg/kg, 3 to 8 mg/kg, 4 to 7 mg/kg, or 5 to 6 mg/kg body weight. For antibodies, the preferred dosage is 0.1 mg/kg to 100 mg/kg of body weight (generally 10 mg/kg to 20 mg/kg). If the antibody is to act in the brain, a dosage of 50 mg/kg to 100 mg/kg is usually appropriate. Generally, partially human antibodies and fully human antibodies have a longer half-life within the human body than other antibodies. Accordingly, lower dosages and less frequent administration is often possible. Modifications such as lipidation can be used to stabilize antibodies and to enhance uptake and tissue penetration (e.g., into the brain). A method for lipidation of antibodies is described by Cruikshank, et al., 1997, J. Acquired Immune Deficiency Syndromes and Human Retrovirology 14:193). The pharmaceutical compositions can be included in a container, pack, or dispenser together with instructions for administration. The invention further provides a kit containing a peptide or polypeptide of the invention of the present invention, o r an antibody or fragments thereof mimicking a polypeptide of the invention, preferably with instructions for use, for example in the treatment of sepsis, septic shock or sepsis-like conditions. The invention provides a method for identifying (or screening) modulators, i.e., candidate or test compounds or agents (e.g., peptides, peptidomimetics, small molecules or other drugs) which mimic a polypeptide of the invention or have a stimulatory or inhibitory effect on, for example, activity of a polypeptide of the invention. In particular, the invention provides a method BXL-P037/PCT 23 of screening compounds or compositions to treat sepsis, septic shock or sepsis-like conditions, comprising: providing a TREM -1 peptide; contacting an animal in a cecal ligation and puncture model (or using other assay or model as described herein or known in the art) with the TREM-1 peptide; determining if there was a modul ation in the sepsis, for example wherein an increase in survival indicates that the TREM-1 peptide may be useful for treating sepsis, septic shock or sepsis-like conditions. The invention further pertains to novel agents identified by the above- described screening assays and uses thereof for treatments as described herein. All publications, including but not limited to patents and patent applications, cited in this specification are herein incorporated by reference as if each individual publication were specifically and individually indicated to be incorporated by reference herein as though fully set forth. Preferred features of each aspect of the invention are applicable to each other aspect, mutatis mutandis. The present invention will now be described with reference to the following non-limiting examples, with reference to the figures, in which: Figure 1A. shows a sequence alignment of TREM -1 and TREM-2 family members. Human TREM-1 was aligned with mouse TREM -1 and human and mouse TREM -2 using version 1.74 of CLUSTAL W. Secondary structure assignments correspond to the published human TREM -1 structure (arrows for p -strands and cylinder for a helices) (Radaev et al. (2003) Structure (Camb).Dec;11(12):1527-35). Residues involved in homo-he terodimer formation are shown in white on black background. Cysteine making disulfide bonds conserved for V- type Ig fold are in bold. Gaps are indicated with (-), identical residues with (*), similar with (: or.). An extended region of similarities between human and mouse TREM1 sequences is shown in boxes on grey background. TREM-1 peptide sequences used in the Examples herein are indicated underlined. Figure 1B. shows a ribbon diagram of the published TREM-1 homodimeric structure (Kelker, et al. (2004) J Mol Biol. Sep 24;342{4):1237 -48). Postulated binding sites that comprise the antibody equivalent Complementarity Determining Regions (CDRs) are in red. Figure 2. shows that administration of TREM-1 peptides, 1 hour before LPS, reduces death induced by endotoxaemla. BALB/c mice (10 per group) were injected intraperitoneally with 200 µg LPS. The TREM-1 peptides P1, P2, P3, or P5 (200 µl of a 300 µM solution per mouse) were injected intraperitoneally 1 hour before LPS. Viability of mice was monitored twice a day for 7 days. Statistical analysis was performed by Logrank test. Data from control mice represent BXL-P037/PCT 24 cumulative survival curves from two independent experiments performed under identical conditions. Figure 3. shows that TREM -1 peptide P1 is able to effectively reduce death induced by endotoxaemia when injected at 4 hours after LPS. BALB/cmice(10 per group) were injected intraperitoneally with 200 µg LPS. TREM -1 peptide P1, 200 µl of a 300 µM solution per mouse was injected intraperitoneally 1 hour before or 4 hours after LPS. Viability of mice was monitored twice a day for 7 days. Statistical analysis was performed with the Logrank test. Data from control mice represent cumulative survival curves from two independent experiments performed under identical conditions Figure 4. shows that administration of TREM-1 peptides, 4 hours after LPS, reduces death induced by endotoxaemia. BALB/c mice (10 per group) were injected intraperitoneally with 200 µg LPS. P1 peptide, 200 µl of a 150, 300 and 600 µM solution per mouse (dots) or P3, 200 µl of a 600 JIM solution per mouse (filled squares) were injected intraperitoneally 4 hours after LPS. Viability of mice was monitored twice a day for 7 days. Statistical analysis was performed with the Logrank test Figure 5. shows that TREM-1 peptide P1 protects against cecai ligation and puncture (CLP). CLP was induced in C57BL/6 mice (15 per group) as described in Materials and Methods. P1 peptide (empty dots) or P3 peptide (filled squares) (200 µl of a 600 µM solution per mouse) were injected intraperitoneally 5 and 24 hours after CLP induction. Viability of mice was monitored twice a day for 10 days. Statistical analysis was performed with the Logrank test. Figure 6. shows that P1, P2 and P5 peptides, but not P3 peptide, inhibit the binding of soluble TREM-1/lgG1 to TREM-1 Ligand positive peritoneal exudate cells. Cytofluorimetric analysis of peritoneal exudate cells with 2 ug/ml of mouseTREM-1/hlgG1 in the presence of a 500µM solution per mouse (thin line), 100µM solution per mouse (dotted line) or absence (thick line) of the peptides is shown. The grey h istogram represents immunostaining with human igG1 as a control. Figure 7A. shows the release of sTREM -1 from cultured monocytes after stim ulation with LPS with and without proteases inhibitor. LPS stimulation induced the appearance of a 27 -kD protein that was specifically recognized by an anti -TREM-1 mAb (inset). sTREM-1 levels in the conditioned culture medium were measured by reflectance o f immunodots. Data are shown as mean ±SD (n=3). BXL-P037/PCT 25 Figure 7B. shows expression of TREM-1 mRNA in monocytes. Cultured monocytes were stimulated with LPS(1ug/mL)forO, 1 and 16 hours as indicated. LPS induced TREM -1 mRNA production within 1 hour. Figure 8A. shows the release of cytokines and sTREM-1 from cultured monocytes. For cell activation, primary monocytes were cultured in 24 -well flat-bottom tissue culture plates in the presence of LPS (1ug/ml_). In some experiments this stimulus was provided in combin ation with P5 {10 to 100 ng/mL), control peptide (10 to 100 ng/mL) or rIL -10 (500 U/mL). To activate monocytes through TREM-1, an agonist anti-TREM-1 mAb(10ug/mL)was added as indicated. Cell-free supernatants were analysed for production of TNF-α, IL -1β and sTREM-1 by ELISA or immunodot. All experiments were performed in triplicate and data are expressed as means (SEM). a: Media b: P5 10 ng/mL c: Anti-TREM-1 d:LPS e: LPS + Anti-TREM-1 f: LPS+ P5 10 ng/mL g: LPS + P5 50 ng/mL h: LPS+ P5 100 ng/mL i: LPS + IL10 Figure 8B. shows the effect of P5 on NFKB activation. Monocytes were cultured for 24 hours in the presence of E.coli LPS (0111 :B4, 1 ug/mL), anti -TREM-1 mAb (10ug/mL) and / or P5 (100 ng/mL) as indicated and the levels of NFKB p50 and p65 were determined using an ELISA- based assay. Experiments were performed in triplicate and data are expressed as means of optical densities (SEM). Figure 9. shows accumulation'of sTREM-1 in serum of LPS- treated mice. Male Balb/C mice (20 to 23 g) were treated with LPS (LD 50, intraperitoneally). Serum was assayed for sTREM-1 by immunodot. Serum sTREM -1 was readily detectable 1 hour after LPS administration and was maintained at a plateau level from 4 to 6 hours. Figure 10A. shows that P5 pre-treatment protects against LPS lethality in mice. Male Balb/C mice (20 to 23g) were randomly grouped (10 mice per group) and treated with an LD 100of LPS. P5(50ug or 100ug) or control vector was administered 60 min before LPS. BXL-P037/PCT 26 Figure 10B. shows that delayed administration of P5 protects LPS lethality in mice. Male Balb/C mice (20 to 23 g) were randomly grouped (8 mice per group) and treated with an LD 100 of LPS. P5 (75ug) or control vector was administered 4 or 6 hours after LPS as indicated. Figure 10C. shows that administration of agonist TREM-1 mAb is lethal to mice. Male Balb/C mice (20 to 23 g) were randomly grouped (8 mice per group) and treated with a combination of an LD50 of LPS + control vector, LD 50 of LPS + anti-TREM-1 mAb (5ug) or LD100 of LPS + control vector as indicated. Control vector and anti -TREM-1 mAb were administered 1 hour after LPS injection Figure 11 A. shows that P5 partially protects mice from CLP-induced lethality. Male Balb/C mice (20 to 23g) were randomly grouped and treated with normal saline (n=14) or the controi peptide (n=14, 100ug)orwith P5 (100ug) in a single infection at HO (n=18), H+4 (n=18) or H+24 (n=18). The last group of mice (n=18) was treated with repeated injections of P5 (100ug) at H+4, H+8 and H+24. Figure 11B. shows the dose effect of P5 on survival. Mice (n=15 per group) were treated with a single injection of normal saline or 10µg, 20µg, 50µg 100µg or 200µg of P5at HO after the CLP and monitored for survival Figure 12. shows that P5 has no effect on bacterial counts during CLP. Mice (5 per group) were killed under anaesthesia at 24 hours after CLP. Bacterial counts in peritoneal lavage fluid and blood were determined and results are expressed as CFU per mL of blood and CFU per mouse for the peritoneal lavage. Figure 13 shows TNF-α and IL-1β plasma concentration evolution after LPS (15mg/kg) administration in rats. * p § p Figure 14 shows Nitrite/Nitrate concentrations evolution after LPS (15mg/kg) administration in rats. * p Figure 15 shows mean arterial pressure evolution during caecal ligation and puncture-induced peritonitis in rats. * p BXL-P037/PCT 27 Figure 16 shows TNF-a plasma concentration evolution during caecal ligation and puncture- induced peritonitis in rats. * p § p $p Figure 17 shows Nitrite/Nitrate concentration evolution during caeca! ligation and puncture - induced peritonitis in rats. * p Example 1: TREM-1 peptides protect mice from death by septic shock. TREM-1 peptides matching the following criteria were synthesized: i) highest homology between human and mouse TREM -1 and lowest homology with TREM-2. ii) peptides spanning the Complementarity Determining Regions (CDRs) of TREM -1. According to the published crystal structure of TREM-1, and in analogy with antibodies, these residues are likely to be involved in cognate ligand recognition (Radaev et al. (2003) Structure (Camb).Dec;11(12):1527- 35 & Kelker, et al. (2004) J Mol Biol. Sep 24;342(4):1237 -48) (see Figure 1). One peptide (P1) was designed in the CDR2 region and three peptides (P2, P4 and P5) in the CDR3 region. A fourth peptide (P3) was designed in the neck region connecting the V-type immunoglobulin (Ig) - like domain (ig-V) to the trans-membrane domain. No peptide was designed in the CDR1 region due to high sequence homology between TREM -1 and TREM-2. Thus, the following peptides of the TREM -1 protein were ordered from and were synthesized and purified by the Protein and Peptide Chemistry Facility, Institute of Biochemistry, University of Lausanne: P1 (CDR2 67-89) LVVTQRPFTRPSEVHMGKFTLKH [SEQ ID NO:3] P2 (CDR3114-136) VIYHPPNDPVVLFHPVRLWTKG [SEQ ID NO:4] P3 (neck region 168-184)TTTRSLPKPTAWSSPG [SEQ ID NO:5] P4 (CDR3 103-123) LQVTDSGLYRCVIYHPPNDPV [SEQ ID NO:6] P5 (CDR3103-119): LQVTDSGLYRCVIYHPP [SEQ ID NO:7] P1sc* (P1 scrambled seq.) LTPKHGQRSTHVTKFRVFEPVML [SEQ ID NO:8] P5sc* (P5 scrambled seq.) TDSRCVIGLYHPPLQVY [SEQ ID NO:9] * This is a control peptide and indeed does not protect BXL-P037/PCT 28 In the experiments of this example, the peptides were admi nistered in a volume of 200µl of the solution molarity indicated. To assess the ability of TREM1-peptides to protect mice from LPS-induced endotoxaemia, the Inventors administered peptides P1, P2, P3 and P5 (300 µM) 1 hour before a lethal dose of lipopolysaccharide (LPS) (Figure 2). Lethality was monitored over time and compared with animals that had received control injections of vehicle alone. P5 injection confers maximal protection, with 90% of the animals still alive 7 days after LPS injection, as compared with 10% of control mice(p 50% of the P2 treated mice survived endotoxaemia as compared with 10% of control mice (p injection. These results indicate that peptides containing sequences of the extracellular portion of TREM-1 corresponding to the putative ligand binding site (CDR2 and CDR3) can protect mice from lethal shock. In order to investigate whether TREM-1 peptide treatment could be d elayed until after the administration of LPS, the Inventors injected the peptides at 4 hours after LPS injection. Only in the case of P1, this delayed treatment conferred significant protection against a lethal dose of LPS (Figure 3). 80 % of the mice injected with P14 hours after LPS survived endotoxaemia compared to 60 % of mice treated 1 h before LPS and 10 % of mice treated with vehicle alone (p the outbreak of endotoxaemia. No late death occurred over one week, indicating that P1 did not merely delay the onset of LPS lethality, but provided lasting protection. P1 administration conferred maximal protection (80 %) when administered at 600 µ M (p protection dropped to 50 % at 300 µM (p compared to 20% of control mice, indicating a dose dependent effect of P1 (Figure 4). The Inventors then investigated whether P1 protects again st septic shock in the "CLP" model (Cecal Ligation and Puncture is a widely used experimental model of sepsis). Mice treated with two doses of P1 at 5 and 24 hours after CLP were protected from death as compared to control treated mice (p=0.0791) although the difference was not statistically significant. 40 % of the mice injected with P1 at 5 days after CLP survived compared to 5 % of mice treated with P3 peptide. At 10 days after CLP, the treated mice were still alive, indicating that P1 did not merely delay mortality, but provided lasting protection (Figure 5). Example 2: TREM-1 peptide P1 inhibits binding of soluble mouse TREM- 1/lgG to TREM-1 ligand positive cells Among TREM-1 derived peptides tested in CLP, peptides P1, P2 and P5 demonstrate a protective activity. A possible mechanism of action could be the ability of TREM -1 derived peptide to interfere with TREM-1/TREM-1 ligand interaction. To address this question the BXL-P037/PCT 29 Inventors performed competition experiments on TREM -1 ligand positive cells: PEC (Peritoneal Exudate Cells) from CLP treated mice. Peritoneal exudate cells (PEC) from mice suffering from a caecal ligation and puncture (CLP)-induced peritonitis were subjected to flow cytometry analysis after incubation with a PE- conjugated anti-human lgG1 (Jackson Immunoresearch, Bar Harbor, USA). Competition with TREM-1 peptides was performed by pre-incubating cells with the indicated concentrations of peptides for 45 minutes on ice before adding mTREM-1-lgG1. As shown in Figure 6, the P1 peptide, derived from the CDR2 region of mTREM -1, and the P2 and P5 peptides spanning the CDR3 region inhibit TREM-1 interaction with its ligand in a dose dependent manner. Conversely the P3 peptide, derived from the neck region of TREM-1 connecting the IgG like portion to the transmembrane domain was ineffective. Example 3: Additional studies on the modulation of the inflammatory response in murine sepsis by TREM-1 peptide P5 Methods Preparation of monocytes from peripheral blood Ten ml_ of peripheral blood samples were collected on EDTA-K from 5 healthy volunteer donors originating from laboratory staff. After dilution in RPMI (Life Technologies, Grand Island, NY) v/v, blood was centrifuged for 30 min at room temperature over a Ficoll gradient (Amersham Pharmacia, Uppsala, Sweden) to isolate PBMC. The cells recovered above the gradient were washed and counted. In order to deplete the suspensions of lymphocytes, celts were then plated in 24-well flat-bottom tissue culture plates (Corning, Corning, NY) at a concentration of 5x106/mL and allowed to adhere during 2 hours at 37°C. The resulting lymphocyte suspension was discarded and the adhering monocytic cells were maintained in a 5% CO2 incubator at 37°C in complete medium (RPMI 1640, 0.1 mM sodium pyruvate, 2 mM Penicillin, 50 µg/mL Streptomycin; Life Technologies) supplemented with 10% FCS (Invitrogen, Cergy, France). TREM-1 peptide Using the human TREM -1 sequence in Gen-Bank, accession #AF287008 and the mouse TREM-1 sequence #AF241219, a peptide "P5" (LQVTDSGLYRCVIYHPP; [SEQ ID NO:7]; was chemically synthesized as a C-terminally amidated peptide (Pepscan Systems, Lelystad, The Netherlands). The correct peptide was obtained in greater than 99% yield and with measured mass of 1961 Da versus a calculated mass of 1962 Da and was homogeneous after preparative purification, as confirmed by mass spectrometry and analytic reversed phase - high performance liquid chromatography. A peptide "P5sc" containing the same amino-acids BXL-P037/PCT 30 than P5 but in a different sequence order (TDSRCVIGLYHPPLQVY; [SEQ ID NO:9] ) was similarly synthesized and served as 'control peptide'. In vitro stimulation of monocytes For activation, monocytes were cultured in the presence of E.coli LPS (0111 :B4, 1 µg/mL, Sigma-Aldrich, La Verpilliere, France). Cell viability was assessed by trypan blue exclusion and by measuring lactate dehydrogenase release. In some experiments, this stimulus was given in combination with TNF-a (5 to 100 ng/mL, R&D Systems, Lille, France), IL-1p (5 to 100 ng/mL, R&D Systems), rlFN-y (up to 100 U/m L, R&D Systems), rlL-10 (500 U/ml, R&D Systems) or up to 100 ng/mL of P5 or control peptide. In order to activate monocytes through TREM -1, an anti-TREM-1 agonist monoclonal antibody (R&D Systems) was added as follows: flat- bottom plates were precoated with 10 µg/mL anti- TREM-1 per well. After thorough washing in phosphate buffered saline (PBS), the monocyte suspensions were added at a similar concentration as above. Some experiments were performed in the presence of protease inhibitors (PMSF and Protease C ocktail Inhibitor; Invitrogen). Ceil-free supernatants were assayed for the production of TNF-a and IL -1pby ELISA according to the recommendations of the manufacturer (BD Biosciences, San Diego, USA). To address the effect of P5 on NF-KB activity in monocytes, an ELISA-based assay was performed (BD Mercury™ Transfactor Kit, BD Biosciences). Monocytes were cultured for 24 hours in the presence of E.coli LPS (O111:B4, 1ug/mL), and/or an agonist anti -TREM-1 monoclonal antibody (10µg/mL), and / or P5 (100 ng/mL). Whole -cell extracts were then prepared and levels of NF- KB p50 and p65 were determined according to the recommendations of the manufacturer. Ali experiments were performed in triplicate and data are expressed as means (SEM). Identification and quantisation of sTREM-1 release Primary monocytes suspensions were cultured as described above. The cells were treated with E.coli LPS (0111 :B4,1 µg/mL) for 24 hours at 37°C. Ceil -conditioned medium was submitted to Western-blotting using an anti -TREM-1 monoclonal antibody (R&D Systems) in order to confirm the presence of 27 kDa material recognized by anti -TREM-1. Soluble TREM-1 levels were measured by assessing the optical intensity of bands on immunodots by means of a reflectance scanner and the Quantity One Quantitation Software (Bio-Rad, Cergy, France) as reported elsewhere (18). Soluble TREM-1 concentration from each sample was determined by comparing the optical densities of the samples with reference to standard curves generated with purified TREM-1. All measurements were performed in triplicate. The sensitivity of this technique allows the detection of sTREM -1 levels as low as 5pg/mL. BXL-P037/PCT 31 TREM-1 RT-PCR Total mRNA was extracted from primary monocytes cultured in the presence of LPS using a TRIzol reagent (I nvitrogen), and reverse transcribed using Superscript RT II (Invitrogen) to generate cDNA. RT-PCR conditions then used for all reactions were 94°C, 30s/65°C, 30s/68°C, 1 min for 30 cycles. Amplification was performed with 2.5 mM MgCl2, 0.2 mM dNTP, 2.0 U Taq polymerase, and 20 pM 5' and 3' oligonucleotide primers (Proligos, Paris, France ). The sequences of the 5' and 3' primer pairs used were the following: for TREM-1 (17) TTGTCTCAGAACTCCGAGCTGC; [SEQ ID NO:10] and GAGACATCGGCAGTTGACTTGG; [SEQ ID NO:11] for TREM-1 sv (19) GGACGGAGAGATGCCCAAGACC; [SEQ ID NO:12] and ACCAGCCAGGAGAATGACAATG; [SEQ ID NO:13] for β-actin (used as housekeeping amplicon) GGACGACATGGAGAAGATCTGG; [SEQ ID NO:14] and ATAGTAATGTCACGCACGATTTCC; [SEQ ID NO:15] PCR products were run on agarose gels and visualized by ethidium bromide staining. LPS-induced endotoxinemia in mice After approval by the local ethical committee, male Balb/C mice (20 to 23g) were randomly grouped and treated with E.coli LPS intraperitoneally (i.p.) in combination with P5 (in 500ul normal saline) or control vector before or after LPS challenge. In some experiments, 5ug of an anti TREM-1 monoclonal antibody was administered i.p. one hour after LPS injection. The viability of mice was examined every hour, or ani mals were sacrificed at regular intervals. Serum samples were collected by cardiac puncture and assayed for TNF-a and IL-1β by ELISA (BD Biosciences), and for sTREM -1 levels by immunodot. CLP polymicrobial sepsis model BXL-P037/PCT 32 Male Balb/C mice (7 to 9 weeks, 20 to 23g) were anaesthetized by i.p. administration of ketamine and xylazine in 0.2 mL sterile pyrogen -free saline. The caecum was exposed through a 1.0 cm abdominal midline incision and subjected to a ligation of the distal half followed by two punctures with a G21 needle. A small amount of stool was expelled from the punctures to ensure patency. The caecum was replaced into the peritoneal cavity and the abdominal incision closed in two layers. After surgery all mice were injected s.c. with 0.5 ml of physiologic saline solution for fluid resuscitation and s.c. every 12 h with 1.25 mg (i.e. 50 µg/g) of imipenem. The animals were randomly grouped and treated with normal saline (n=14), the control peptide (n=14, 100µg) or P5 (100µg) in a single injection at HO ( n=18), H+4 (n=18) or H+24 (n=18). The last group of mice (n=18) was treated with repeated injections of P5 (100ug) at H+4, H+8 and H+24. All treatments were diluted into 500ul of normal saline and administered i.p. The inventors next sought to determine th e effect of various doses of P5. For this purpose, mice (n=15 per group) were treated with a single injection of normal safine or 10ug, 20ug, 50ug 10Oµg or 200ug of P5 at HO after the CLP and monitored for survival. Five additional animals per group were killed under anaesthesia 24 hours after CLP for the determination of bacterial count and cytokines levels. Peritoneal lavage fluid was obtained using 2mL RPMI 1640 (Life Technologies) and blood was collected by cardiac puncture. Concentrations of TNF -a and IL-1β in the serum were determined by ELISA (BD Biosciences). For the assessment of bacterial counts, blood and peritoneal lavage fluid were plated in serial log dilutions on tryptic soy supplemented with 5% sheep blood agar pla tes. After plating, tryptic soy agar plates were incubated at 37°C aerobically for 24 hours, and anaerobically for 48 hours. Results are expressed as CFU per mL of blood and CFU per mouse for the peritoneal lavage. Statistical analyses Serum sTREM-1 and cytokines levels were expressed as mean (±SD).The protection against LPS lethality by P5 was assessed by comparison of survival curves using the Log -Rank test. All statistical analyses were completed with Statview software (Abacus Concepts, Berkeley CA) and a two-tailed P Results A soluble form of TREM-1 is released from cultured human monocytes after stimulation with E.coli LPS To identify the potential release of sTREM-1 in vitro, the Inventors stimulated human monocytes with LPS and analyzed the conditioned culture medium by SDS-PAGE. LPS stimulation induced the appearance of a 27 -kDa protein in a time-dependent manner (Figure 7A). Western blotting analysis revealed that this protein was specifically recognized by a BXL-P037/PCT 33 monoclonal antibody directed against the extra-cellular domain of TREM-1 (Figure 7A). Cell viability was unaffected at LPS concentrations that induced the presence of sTREM -1 in conditioned medium, indicating that TREM-1 release was not due to cell death. Similarly, treatment of monocytes with protease inhibitors did not affect TREM-1 release ( Figure 7A). TREM-1 mRNA levels were increased upon LPS treatment ( Figure 7B) whereas TREM -1sv mRNA levels remained undetectable. This suggests that TREM -1 release is likely to be linked to an increased transcription of the gene and unrelated to TREM-1 sv expression. Stimulation of monocytes for 16 hours with TNF -a (5 to 100 ng/mL) or IL-1β (5 to 100 ng/mL) induced very small TREM-1 release in a cytokine dose-dependent manner. Stimulation with IFN-y did not induce TREM-1 release, even at concentrations of up to 100 U/mL LPS associated release of pro-inflammatory cytokines is attenuated by P5 Significant TNF-a and IL-1β production was observed in the supernatant of monocytes cultured with LPS. TNF-α and IL-1 β production was even higher for cells cultured with both TREM-1 mAb and LPS as compared with those cultured with mAb or LPS alone ( Figure 8A). The inducible release of pro-inflammatory cytokines was significantly lowe r after LPS stimulation when the medium was supplemented with P5 or IL-10. P5 reduced, in a concentration- dependent manner, the TNF- α and IL-1 β production from cells cultured with LPS or with LPS and mAb and simultaneously increased the release of sTREM -1 from cells cultured with LPS. The control peptide displayed no action on cytokines or sTREM -1 release (data not shown). In striking contrast, IL-10 totally inhibited the release of both TREM -1 and inflammatory cytokines (Figure 8A). Both LPS and TREM-1 mAb induced a strong activation of monocytic NF -KB p50 and p65 and combined administration of LPS and TREM-1 mAb lead to a synergistic effect. P5 inhibited the NF-KB activation induced by the engagement of TREM-1 but did not alter the effect of LPS (Figure 8B). Serum sTREM-1 levels of LPS-treated mice are increased In order to determine whether sTREM -1 was released systemically during endotoxemia in mice, the Inventors measured serum sTREM-1 levels after LPS administration. Serum sTREM-1 was readily detectable 1 hour after administration of an LD50 dose of LPS and was maintained at peak plateau levels from 4 to 6 hours after LPS treatment ( Figure 9). TREM-1 peptide "P5" protects endotoxemic mice from lethality Mice treated by a single dose of P5 60 min before a lethal dose (LD100) of LPS were prevented from death in a dose -dependent manner (Figure 10A). In order to investigate whether P5 treatment could be delayed until after the administration of LPS, the Inventors injected P5 beginning 4 or 6 hours afte r LPS injection. This delayed treatment up to 4 hours conferred BXL-P037/PCT 34 significant protection against a LD 100 dose of LPS (Figure 10B). No late death occurred over one week, indicating that P5 did not merely delay the onset of LPS lethality, but provided lasting protection. Control mice all developed lethargy, piloerection, and diarrhoea before death. By contrast, P5-treated mice remained well groomed and active, had no diarrhoea, and were lively. To clarify the mechanism by which P5 protected mice from LPS lethality, the Inventors determined the serum levels of TNF -α, IL-1β and sTREM-1 of endotoxemic mice at 2 and 4 hours. As compared to controls, pre -treatment by 100 µg of P5 reduced cytokines levels by 30% and increased sTREM-1 levels by 2 fold as shown in Table 4: Table 4. Serum concentrations of TNF-a, IL-13 and sTREM-1 in endotoxemic mice. TNF-α (ng/mL) IL-1 β (ng/mL) sTREM-1 (ng/mL) H2 H4 H2 H4 H2 H4 Control 3.3±1.0 0.4±0.1 0.3±0.1 1.5±0.2 249±48 139±8 P5(100ug) 2.4±0,5 0.1±0.1 0.2±0.1 0.9±0.2 475±37 243±28 Engagement of TREM-1 is lethal to mice To further highlight the role of TREM-1 engagement in LPS- mediated mortality, mice were treated with agonist anti -TREM-1 mAb in combination with the administration of an LD 50 dose of LPS. This induced a significant increase in mortality rate from 50% to 100% ( Figure 10C). P5 protects mice from CLP-induced lethality To investigate the role of P5 in a more relevant model of septic shock, the Inventors performed CLP experiments (Figure 11A). The control groups comprised mice inj ected with normal saline or with the control peptide. In this model of polymicrobial sepsis, P5 still conferred a significant protection against lethality even when administered as late as 24 hours after the onset of sepsis. Interestingly, repeated injections of P5 had the more favourable effect on survival (P cytokine production (Table 5). P5 had no effect on bacterial clearance ( Figure 12). Table 5. Serum concentrations of T NF-a, IL-13 and sTREM-1 at 24 hours after CLP. TNF-a (pg/mL) IL-1β (pg/mL) sTREM-1 (ng/mL) BXL-P037/PCT 35 Control peptide 105±12 841±204 52±3 Control saline 118±8 792±198 35±5 P5 10µg 110±11 356±62 43±8 P5 20µg 89±10 324±58 58±8 P5 50µg 24±6 57±11 93±10 P5 100µg 20±3 31 ±3 118±12 P5 200µg 21 ±7 37±8 158±13 Sepsis exemplifies a complex clinical syndrome that results from a harmful or damaging host response to severe infection. Sepsis develops when the initial, appropriate host response to systemic infection becomes amplified, and then dysregulated (4, 5). Neutrophils and monocyte/macrophages exposed to LPS, for instance, are activated and release such pro- inflammatory cytokines as TNF-a and IL-1β. Excessive production of these cytokines is widely believed to contribute to the multi-organ failure that is seen in septic patients (20-23). TREM-1 is a recently identified molecule involved in monocytic activation and inflammatory response (12, 14). It belongs to a family related to NK cell receptors that activate downstream signalling events. The expression of TREM -1 on PNNs and monocytes/macrophages has been shown to be inducible by LPS (16, 17). As described herein, the Inventors demonstrate that a soluble form of TREM-1 was released from cultured human monocytes after stimulation with E.coii LPS. Such a soluble form was also detectable in the serum of endotoxemic mice as early as 1 hour after LPS challenge. This is consistent with the implication of TREM -1 in the very early phases of the innate immune response to infection (14, 15, 24). The mechanism by which sTREM-1 is released is not clearly elucidated but seems to be related to an increased transcription of the TREM- 1 gene. Nevertheless, although incubation with a protease inhibitor cocktail does not alter the sTREM-1 release, cleavage of the surface TREM -1 from the membrane cannot be totally excluded. Interestingly, stimulation of human monocytes with such pro -inflammatory cytokines as TNF-a, IL-1β or IFN-Y induced very small sTREM-1 release unless LPS was added as a co -stimulus. The expression of an alternative mRNA TREM -1 splice variant (TREM-1sv) has been detected in monocytes that might translate into a soluble receptor (18) up on stimulation with cell wall fraction of Mycobactehum bovis BCG but not LPS (25). This was confirmed in this study as i) LPS did not increase the level of mRNA TREM-1sv in monocytes and ii) only a 27- kDa protein was released by monocytes upon LPS stimula tion and not the 17.5-kDa variant. Although its natural ligand has not been identified (13,14), engagement of TREM-1 on monocytes with an agonist monoclonal antibody resulted in a further enhancement of pro - BXL-P037/PCT 36 inflammatory cytokines production, while P5 induced a decrease of these syntheses in a concentration-dependent manner, and IL -10 completely suppressed it. Inflammatory cytokines, and especially TNF -a, are considered to be deleterious, yet they also possess beneficial effects in sepsis (5) as shown by the fatal issue of peritonitis in animals with impaired TNF-a responses (9-11). Moreover, in clinical trials, the inhibition of TNF-α increased mortality (8). Finally, the role of TNF- a in the clearance of infection has been highlighted by the finding that sepsis is a frequent complication in rheumatoid arthritis patients treated with TNF-a antagonists (26). The mechanism by which P5 modulates cytokine production is not yet clear. P5 comprises the complementary determining region (CDR)-3 and the lF' |3 strand of the extra - cellular domain of TREM -1. The latter contains a tyrosine residue mediating dimerization. Radaev et al postulated that TREM -1 captures its ligand with its CDR- equivalent loop regions (27). P5 could thus impair TREM-1 dimerization and / or compete with the natural ligand of TREM-1. Moreover, the increase of sTREM -1 release from monocytes mediated by P5 could prevent the engagement of membrane TREM-1, sTREM-1 acting as a decoy receptor, as in the TNF-a system (28, 29). Activation of the transcription factor NF-KB is a critical step in monocyte inflammatory cytokine production after exposure to bacterial stimuli such as LPS (30, 31). Among the various NF-KB / Rel dimers, the p65 / p50 heterodimer is the prototypical form of LPS-inducible NF -KB in monocytes (32), P5 abolishes the p65 / p50 NF-KB over-activation induced by the engagement of TREM-1. This might at least partially explain the effects of P5 on cytokine production and the protection from lethality shown here to occur when the peptide was injected one hour before LPS-induced septic shock, or even up to 4 hours after. Endotoxemia is simple to achieve experimentally, but imperfectly suited to reproduce human sepsis, while polymicrobial sepsis induced by CLP is a more complex but better model, including the use of fluid resuscitation and antibiotics. The latter was thus also used in this study, and confirmed the dose-dependent protection provided by P5, even when administered as late as 24 hours after the onset of sepsis. The favourable effect of P5 was however unrelated to an enhanced bacterial clearance. One difficulty in the use of immunomodulatory therapies is that it is not possible to predict the development of sepsis, and, thus, patients receiving those treatments frequently already have well-established sepsis (6). Since P5 appeared to be effective even when injected after the outbreak of sepsi s, it could thus constitute a realistic treatment (24, 33). By contrast, engagement of TREM-1 by an agonist anti- TREM-1 monoclonal antibody mediated a dramatic increase of mortality rate in LPS-challenged mice: this further underscores the detrimental effect of TREM-1 engagement during septic shock. BXL-P037/PCT 37 Experimental septic shock reproduces human sepsis only in part. Indeed, our group recently showed that significant levels of sTREM-1 were released in the serum of critically ill patients with sepsis patients (34), the highest levels being observed in patients who survived. This is consistent with our experimental findings indicating that the more important sTREM-1 release, the more favourable is the outcome, and thus sustains, at least theoretically, the potential value of soluble TREM peptides as post- onset sepsis therapy. TREM-1 appears to be a crucial player in the immediate immune response triggered by infection. In the early phase of infection, neutrophils and monocytes initiate the inflammatory response owing to the engagement of pattern recognition receptors by microbial products β, 4). At the same time, bacterial products induce the up -regulation and the release of sTREM-1. Upon recognition of an unknown ligand, TREM -1 activates signalling pathways which amplify these inflammatory responses, notably in monocytes/macrophages. The modulation of TREM -1 signalling reduces, although without complete inhibition, cytokine production and protects septic animals from hyper-responsiveness and death. Modulation of TREM-1 engagement with such a peptide as P5 might be a suitable therapeutic tool for the treatment of sepsis, particularly because it seems to be active even after the onset of sepsis following infectious aggression. Example 4: Haemodvnamic studies in LPS treated and septic rats treated with P1 and P5 The role of TREM-1 peptides in further models of septic shock, was investigated by performing LPS and CLP (caecal ligation and puncture) experiments in rats. Materials and Methods LPS-induced Endotoxinemia Animals were randomly grouped (n=10-20) and treated with Escherichia coli LPS (O111:B4, Sigma-Aldrich, Lyon, France) i.p. in combination with the TREM -1 or scrambled peptides. CLP Polymicrobial Sepsis Model The procedure has been described in details els ewhere {see Mansart, A. et al. Shock 19:38-44 (2003)). Briefly, rats (n=6-10 per group) were anesthetized by i.p. administration of ketamine (150 mg/kg). The caecum was exposed through a 3.0 -cm abdominal midline incision and subjected to a ligation of the distal half followed by two punctures with a G21 needle. A small amount of stool was expelled from the punctures to ensure potency. The caecum was replaced into the peritoneal cavity and the abdominal incision closed in two layers. After surgery, all rats were injected s.c. with 50 mL/kg of normal saline solution for fluid resuscitation. TREM-1 or scrambled peptides were then administered as above. BXL-P037/PCT 38 Haemoclvnamic Measurements in rats Immediately after LPS administration as well as 16 hours after CLP, arterial BP (systolic, diastolic, and mean), heart rate, abdominal aortic blood flow, and mesenteric blood flow were recorded using a procedure described elsewhere (see Mansart, A. et al. Shock 19:38-44 (2003)). Briefly, the left carotid artery and the left jugul ar vein were cannulated with PE -50 tubing. Arterial BP was continuously monitored by a pressure transducer and an amplifier- recorder system (lOX EMKA Technologies, Paris, France). Perivascular probes (Transonic Systems, Ithaca, NY) wrapped up the upper abd ominal aorta and mesenteric artery, allowed to monitor their respective flows by means of a flowmeter (Transonic Systems). After the last measurement (4th hour during LPS experiments and 24th hour after CLP), animals were sacrificed by an overdose of sodiu m thiopental i.v. Biological Measurements Blood was sequentially withdrawn from the left carotid artery. Arterial lactate concentrations and blood gases analyses were performed on an automatic blood gas analyser (ABL 735, Radiometer, Copenhagen, Denmark). Concentrations of TNF-a and IL-1β in the plasma were determined by an ELISA test (Biosource, Nivelles, Belgium) according to the recommendations of the manufacturer. Plasmatic concentrations of nitrates/nitrites were measured using the Griess reaction (R&D Systems, Abingdon, UK). Statistical analyses Results are expressed as mean±SD. Between -group comparisons were performed using Student' f tests. All statistical analyses were completed with Statview software (Abacus Concepts, CA) and a two-tailed P Results Endotoxinemia model Following LPS administration, arterial pressures, aortic and mesenteric blood flows dropped rapidly in control animals (scrambled peptides treated rats) while the heart rate remained unchanged (Table 6). The decrease of arterial pressures and aortic blood flow was delayed until the second hour in TREM-1 peptide treated animals with significantly higher values by that time than in control animals. There was no difference between P1 and P5 treated groups. By contrast, none of these two peptides had any effect on the decrease of the mesenteric blood flow (Table 6). BXL-P037/PCT 39 Arterial pH remained constant over time until the fourth hour after LPS injection where it severely dropped in the control group only (Table 6). The significant arterial lactate level elevation present in control animals after the third hour was abolished by the TREM -1 peptides (Table 6). There was no difference between P1 and P5 with regard to pH, arterial bicarbonate and lactate concentration s. As expected, a peak of TNF-a plasmatic concentration was induced by LPS between 30 minutes and 1 hour after injection followed by a progressive decline thereafter ( Figure 13A). P1 peptide injection had no effect on this production, while P5 attenuated TNF-a production by -30%. P1 delayed the IL-1β peak until the third hour after LPS injection, but without attenuation. By contrast, P5 strongly reduced IL-1β release ( Figure 13B). Nitrite/nitrate concentrations increased rapidly after LPS administration in con trol and P1 treated animals but remained stable upon P5 treatment ( Figure 14). BXL-P037/PCT 40 Table 6. Hemodynamic parameters during LPS-induced endotoxinemla CLP Model As the severity of the Inventors' model was at its highest 16 to 20 hours after the completion of the CLP, the Inventors chose to investigate animals by the 16th hour. Importantly, there were no deaths before this time point. Although all animals were fluid resuscitated, none received antibiotics in order to strictly consider the role of the peptides. BXL-P037/PCT 41 There was a dramatic decline in arterial pre ssure in the control animals over time, and by H24 systolic, diastolic and mean arterial pressures were 58±7 mmHg, 25±4 mmHg and 38±2 mmHg respectively. This decrease was almost totally abolished with P1 or P5 treatment with no significant difference between H16 and H24 (Figure 15). There was no difference between P1 and P5 treated rats. TREM-1 peptides also prevented the aortic and mesenteric blood flows decrease observed in control animals (Table 7). The protective effect on mesenteric blood flow alterations was even higher under P5 treatment. The relative preservation of blood flows was not related to an increased heart rate, since the latter was rather slower than in control animals (Table 7 ). The progressive metabolic acidosis that developed in control rats was attenuated by the P1 peptide, and almost abrogated by P5. The same protective trend was observed for arterial lactate elevation with a more pronounced effect of P5 (Table 7 ). Table 7. Hemodynamic and selected biochemical parameters during CLP polymicrobial sepsis BXL-P037/PCT 42 Both P1 and P5 induced a decrease in TNF- a production, again with a stronger effect of P5. By H20, plasmatic TNF-α was almost undetectable under P5 treatment whereas it remained elevated in the other groups of animals ( Figure 16). Nitrite/nitrate concentrations were increased in control animals but remained at a low level in both TREM-1 peptides treated groups (Figure 17). A protective action of both P5 and P1 on hemodynamics was thus observed in septic rats. Both arterial pressure and blood flows were preserved, independently of heart rate. Moreover, modulation of TREM -1 signalling reduced, although not completely, cytokine production and protected septic animals from hyper-responsiveness. The fact that the cytokine production was not totally inhibited is a crucial point. Indeed, although inflammatory cytokines such as TNF-a are considered deleterious, they also display beneficial effects in sepsis as underlined by the fatal issue of peritonitis models in animals with impaired TNF-a responses. The activation of iNOS observed during septic shock leads to the production of large amount of NO that partly explains some of the peripheral vascular disorders (notably vasodilation and hypotension). On the myocardium itself, most of the action of NO is mediated by an activation of the soluble guanylate-cyclase responsible for the production of cGMP which impairs the effect of cytosolic calcium on contraction. Cyclic GMP is also able to stimulate the activity of some phosphodiesterases. The subsequent decrease of intra -cellular cAMP levels could explain the ability of NO to attenuate the effects of beta adrenergic stimulation. The preservation of arterial pressure could therefore be partly explained by a lessened production of NO, as reflected by the lower concentrations of plasma nitrite/nitrate in TREM-1 peptides treated animals. The decrease in inflammatory cytokine production could partly explain the effect noted on blood flows. Indeed, although the list of potential cytokine mediators of myocardial depression is long, TNF-a and IL-1p have been shown to be good candidates Both these latter cytokines depressed myocardial contractility in vitro or ex vivo. Moreover, the neutralization or removal of TNF-a or IL-1β from human septic serum partly abrogates the myocardial depressant effect in vitro and in vivo. Although P1 and P5 had an identical action on blood flows and arterial pressure during endotoxinemia, their action on cytokine production differed with only a slight effect of P1 on plasma TNF-a and IL-1β concentrations. The protective role of the TREM-1 peptides could therefore be only partly related to their action on cytokine release, or involve redundant pathways. The modulation of the TREM-1 pathway by the use of small synthetic peptides had beneficial effects on haemodynamic parameters during experimental septic shock in rats, along with an attenuation of inflammatory cytokine production. BXL-P037/PCT 43 In summary, these data show that the TREM-1 peptides of the invention 1) efficiently protect subject animals from sepsis -related hemodynamic deterioration; 2) attenuate the development of lactic acidosis; 3) modulate the production of such pro-inflammatory cytokines as TNF-a and IL-1β and 4) decrease the generation of nitric oxide. Thus TREM-1 peptides are potentially useful in the restoration of haemodynamic parameters in patients with sepsis, septic shock or sepsis-like conditions and therefore constitute a potential treatment for the aforesaid conditions. References 1. Aderem, A, and R. J. Ulevitch, R. J. 2000. Toll -like receptors in the induction of the innate immune response. Nature 406:782-786. 2. Thoma-Uszynski, S-, S. Stenger, 0. Takeuchi, M.T. Ochoa, P.A. Engeie, P.A. Sieiing, P.F. Barnes, M. Rollinghoff, P.L. Bolcskei, and M. Wagner. 2001. Induction of direct antimicr obial activity through mammalian Toll-like receptors. Science 291:1544-1549. 3. Medzhitov, R., and C Jr. Janeway. 2000. Innate immunity. N. Engl. J. Med. 343:338-344. 4. Cohen, J. 2002. The immunopathogenesis of sepsis. Nature 420:885-91. 5. Hotchkiss, R.S., and I.E. Karl. 2003. The pathophysiology and treatment of sepsis. N. Engl. J. Med 348:138-50. 6. Vincent, J.L., Q. Sun, and M.J. Dubois. 2002. Clinical trials of immunomodulatory therapies in severe sepsis and septic shock. Clin. Infect. Dis. 34:1084-1093. 7. Riedemann, N.C., R.F. Guo, and P. Ward. 2003. Novel strategies for the treatment of sepsis. Nat. Med. 9:517-524. 8. Fisher, C.J.Jr., J.M, Agosti, S.M. Opal, S.F. Lowry, R.A. Balk, J.C. Sadoff, E. Abraham, R.M. Schein, and E. Benjamin. 1996. Treatment of septic shock with the tumor necrosis factor receptorFc fusion protein. The Soluble TNF Receptor Sepsis Study Group. N. Engl. J. Med 334:1697-702. 9. Echtenacher, B., W. Falk, D.N. Mannel, and P.H. Krammer. 1990. Requirement of endogenous tumor necrosis factor/cachectin for recovery from experimental peritonitis. J. Immunol. 145:3762-3766. 10. Echtenacher, B., K. Weigl, N. Lehn, and D.N. Mannel. 2001. Tumor necrosis factor- dependent adhesions as a major protective mechanism early in septic peritonitis in mice. Infect. Immun. 69:3550-5. 11. Eskandari, M.K., G. Bolgos, C. Miller, D.T. Nguyen, L.E. DeForge, and D.G. Remick. 1992. Anti-tumor necrosis factor antibody therapy fails to prevent lethality after cecal ligation and puncture or endotoxemia. J. Immunol. 148 :2724-30. BXL-P037/PCT 44 12. Bouchon, A., J. Dietrich, and M. Colonna. 2000. inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes. J. Immunol. 164:4991-4995. 13. Colonna, M., and F. Facchetti. 2003. TREM -1 (triggering receptor expressed on myeloid cells): a new player in acute inflammatory responses. J. Infect. Dis. 187 (Suppl) :S297-301. 14. Colonna, M. 2003. TREMs in the immune system and beyond. Nat. Rev, Immunol. 6:445- 453. 15. Nathan, C, and A. Ding. 2001. TREM-1: a new regulator of innate immunity in sepsis syndrome. Nat Med. 7:530-2. 16. Bouchon, A., F. Facchetti, M.A. Weigand, and M. Colonna. 2001. TREM -1 amplifies inflammation and is a crucial mediator of septic shock. Nature 410:1103-1107. 17. Bleharski, J.R., V. Kiessler, C. Buonsanti, P.A. Sieting, S. Stenger, M. Colonna, and R.L. Modlin. 2003. A role for Triggering Receptor Expressed on Myeloid cells -1 in host defense during the early-induced and adaptive phases of the immune response. J. Immunol. 170:3812-3818. 18. Gibot, S., A. Cravoisy, B. Levy, M.C. Bene, G. Faure, and P.E. Bollaert. 2004. Soluble triggering receptor expressed on myeloid cells and the diagnosis of pneumonia. N. Engl. J. Med. 350:451-8. 19. Gingras, M.C, H. Lapillonne, and J.F. Margolin. 2001. TREM -1, MDL-1, and DAP12 expression is associated with a mature stage of myeloid development. Mol. Immunol. 38:817-24. 20. Dinarello, C.A. 1997. Pro inflammatory and anti -inflammatory cytokines as mediators in the pathogenesis of septic shock. Chest 112 (suppl):S21-9. 21. Bone, R.C., R.A Balk, F.B. Cerra, R.P. Dellinger, W.A. Knauss, R.M. Schein, and W.J. Sibbald.1992. Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine. Chest 101:1644-55. 22. Warren, H.S. 1997. Strategies for the treatment of sepsis. N. Engl. J. Med .336:952-3. 23. Stone, R. 1994. Search for sepsis drugs goes on despite p ast failures. Science 264:365-7. 24. Cohen, J. 2001. TREM-1 in sepsis. Lancet 358:776-8. 25. Begun, N.A., K. lshii, M. Kurita-Taniguchi, M. Tanabe, M. Kobayashi, Y. Moriwaki, M. Matsumoto, Y. Fukumori, I. Azuma, K. Toyoshima, and T. Seya. 2004. Mycobacterium bovis BCG cell wall-specific differentially expressed genes identified by differential display and cDNA substraction in human macrophages. Infect.lmmun. 12:937-48. BXL-P037/PCT 45 26. Keane, J., S. Gershon, R.P. Wise, E. Mirabile-Levens, J. Kasznica, W.D. Schwieterman, J.N. Siegel, and M.M. Braun. 2001. Tuberculosis associated with infliximab, a tumor necrosis factor alpha-neutralizing agent. N. Engl. J. Med. 345:1098-104. 27. Radaev, S., M. Kattah, B. Rostro, M. Colonna, and P. Sun. 2003. Crystal structure of the human myeloid cell activating receptor TREM-1. Structure 11:1527 -35. 28. Lantz, M., U. Gullberg, and E. Nilsson. 1990, Characterization in vitro of a human tumor necrosis factor binding protein. A soluble form of tumor necrosis factor receptor. J. Clin. invest. 86:1396-1401. 29. van Zee, K.J., T. Kohno, and E. Fischer. 1992. Tumor necrosis soluble receptors circulate during experimental and clinical inflammation and can protect against excessive tumor necrosis factor a in vitro and in vivo. Proc. Natl. Acad. Sci. USA 89:4845-4853. 30. Collart, MA, P. Baeuerle, and P. Vassalli. 1990. Regulation of tumor necrosis factor alpha transcription in macrophages. Involvement of four NF KB motifs and constitutive and inducible form of NFKB. Mol. Cell Biot. 10:1498-506. 31. Hiscott, J.M., J.J. Garoufalis, A. Roulston, I. Kwan, N. Pepin, J. Lacoste, H. Nguyen, G. Bensi, and M. Fenton. 1993. Characterization of a functional NF KB site in the human IL-1β promoter: evidence for a positive autoregulatory loop. Mol. Cell Biol. 13:6231-40. 32. Urban, M.B., R. Schreck, and P.A. Baeuerle. 1991. NFKB contacts DNA by a heterodimer of the p50 and p65 subunit. EMBO J. 10:1817-25. 33. Lolis, E., and R. Bucala. 2003. Therapeutic approaches to innate immunity: severe sepsis and septic shock. Nat Rev. Drug. Discov. 2:635-45. 34. Gibot, S., M.N. Kolopp-Sarda, M.C. Bene, A. Cravoisy, B. Levy, G. Faure, and P.E. Bollaert. 2004. Plasma level of a triggering receptor expressed on myeloid ceils-1: its diagnostic accuracy in patients with suspected sepsis. Ann. Intern. Med. 141:9 -15. BXL-P037/PCT 46 CLAIMS 1. A polypeptide comprising one or more sequences derived from CDR2 or CDR3 of a TREM-1 protein, characterised by the ability to treat, ameliorate, or lessen the symptoms of sepsis, septic shock or sepsis-like conditions. 2. A polypeptide according to claim 1 wherein said polypeptide comprises fewer than 30 contiguous amino acids of said TREM-1 protein. 3. A TREM-1 polypeptide having anti-sepsis or anti -septic shock activity which consists of (i) a contiguous sequence of 15-25 amino acids corresponding to a native TREM-1 protein sequence which includes at least 3 amino acids from the CDR2 or CDR3 sequences; or (ii) such a sequence in which one or more amino acids are substituted conservatively with another amino acid provided, however that at least 3 a mino acids from the CDR2 or CDR3 sequences are not substituted; or (iii) a sequence of (i) or (ii) linked at one or both of its N and C termini to a heterologous poiypeptide. 4. A poiypeptide according to claim 3 wherein the native TREM -1 protein sequence is the human sequence identified as SEQ ID No 1 and the CDR2 and CDR3 sequences are RPSKNS and QPPKE respectively. 5. A polypeptide according to claim 4 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are QPP. 6. A polypeptide according to claim 4 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are QPPK. 7. A polypeptide according to claim 4 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are QPPKE. 8. A polypeptide according to claim 4 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are RPSKNS. 9. A polypeptide according to claim 3 wherein the native TREM -1 protein sequence is the mouse sequence identified as SEQ ID NO: 2 and the CDR2 and CDR3 sequences are RPFTRP and HPPND respectively. BXL-P037/PCT 47 10. A polypeptide according to claim 9 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are HPP. 11. A polypeptide according to claim 9 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are HPPN. 12. A polypeptide according to claim 9 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are HPPND. 13. A polypeptide according to claim 9 wherein the at least 3 amino acids from the CDR2 or CDR3 sequences are RPFTRP. 14. A polypeptide according to any of the preceding claims wherein said polypeptide is characterised by the ability to treat, ameliorate, or lessen the symptoms of sepsis, septic shock or sepsis-like conditions. 15. A polypeptide having substantial sequence identity to sequence any one of SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19 and characterised by the ability to treat, ameliorate, or lessen the symptoms of sepsis, septic shock or sepsis-like conditions 16. A polypeptide of sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19, its ac tive fragments, analogues, and derivatives, and characterised by the ability to treat, ameliorate, or lessen the symptoms of sepsis, septic shock or sepsis-like conditions. 17. A polypeptide having at least 80% sequence identity to the sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19 and characterised by the ability to treat sepsis, septic shock or sepsis -like conditions and having at least two consecutive amino acids derived from CDR2 or CDR3 of a TREM-1 protein. 18. A poiypeptide having at least 80% sequence identity to the sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19 and characterised by the ability to treat sepsis, septic shock or sepsis -like conditions, wherein the peptide has at least three consecutive amino acids derived from CDR2 or CDR3 of a TREM-1 protein. 19. An isolated polynucleotide capable of encoding a polypeptide having substantial sequence identity to the sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17,18 or 19 and characterised by the ability to treat sepsis, septic shock or sepsis-like conditions . BXL-P037/PCT 48 20. A vector which contains a polynucleotide capable of encoding a polypeptide having at least about 80% sequence identity to the sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19 and characterised by the ability to treat sepsis, septic shock or sepsis-like conditions 21. A polypeptide according to any one of claims 15 to 20 wherein said polypeptide comprises less than 30 contiguous amino acids of a native TREM -1 protein. 22. A composition comprising a peptide or polypeptide of any one of the preceding claims 23. The peptide or polypeptide of any one of the preceding claims for use in therapy 24. The peptide or poiypeptide of any one of the preceding claims for use in therapy in the treatment of sepsis, septic shock or sepsis-like co nditions 25. Use of the peptide or polypeptide of any one of the preceding claims in the manufacture of a medicament for the treatment of sepsis, septic shock or sepsis -like conditions 26. A method of treating or ameliorating sepsis, septic shock or sepsis-like conditions in a subject, comprising: administering a therapeutically effective amount of a peptide or polypeptide of any one of the preceding claims to a subject 27. The method of claim 26 where in said peptide or polypeptide has substantial sequence identity to sequence SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19. 28. The method of claim 26, wherein said peptide or polypeptide is SEQ ID NOS: 3, 4, 6, 7, 16, 17, 18 or 19 or an active fragment, analogue or derivative of SEQ ID NOS: 3, 4, 6, 7, 16, 17 , 18 or 19 29. The method of claim 26, wherein said peptide or polypeptide has at least about 80% sequence identity to SEQ ID NOS: 3, 4, 6, 7,16, 17, 18 or 19 30. A method of screening compounds or compositions to treat sepsis, septic shock or sepsis-like conditions, comprising: providing a TREM-1 peptide or TREM-1 polypeptide; contacting an animal in a suitable model with the TREM -1 peptide; BXL-P037/PCT 49 determining if there was a modul ation in the sepsis, wherein an increase in survival indicates that the TRE M-1 peptide may be useful for treating sepsis, septic shock or sepsis -like conditions. 31. A polypeptide, vector use, method or composition according to any one of the preceding claims wherein the indication is sepsis or septic -shock. A pc ypeptide comprising one or more sequences derived from CDR2 or DR3 of a TREM- 1 protein, characterised by the ability to treal, ameliorate or lessen the symatoms of sepsis, 5 sept c shock or sepsis-IiKe conditions. |
|---|
| Patent Number | 270220 | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Indian Patent Application Number | 1045/KOL/2005 | |||||||||||||||
| PG Journal Number | 49/2015 | |||||||||||||||
| Publication Date | 04-Dec-2015 | |||||||||||||||
| Grant Date | 02-Dec-2015 | |||||||||||||||
| Date of Filing | 18-Nov-2005 | |||||||||||||||
| Name of Patentee | NOVO NORDISK A/S | |||||||||||||||
| Applicant Address | NOVO ALLE, DK-2880 BAGSVAERD, DENMARK | |||||||||||||||
Inventors:
|
||||||||||||||||
| PCT International Classification Number | A61K47/48 | |||||||||||||||
| PCT International Application Number | N/A | |||||||||||||||
| PCT International Filing date | ||||||||||||||||
PCT Conventions:
|
||||||||||||||||