Title of Invention

PEPTIDES OF IL1 BETA AND TNF ALPHA

Abstract The present invention relates to peptides derived from the proinflammatory cytokines, interleukin-1ß, (IL1ß) and tumor necrosis factor &agr;, (TNF&agr;), and their use in human or veterinary therapy, such as to generally treat diseases linked to the overproduction of IL1ß or TNF&agr; as well as acute or chronic inflammatory diseases, rheumatoid arthritis, septic shock, autoimmune diabetes, graft rejection in the host, etc.
Full Text

PEPTIDES OF IL1 BETA AND TNF ALPHA AMD METHOD OF TREATMENT USING
SAME
BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to new peptides derived from the proinflammatory cytokines Interleukin-1 beta (IL1β) and Tumor Necrosis Factor alpha (TNFα) and their use in human or veterinary therapy. The diseases targeted by these therapeutic uses can be ,in particular rheumatoid polyarthritis, septic shock, auto-immune diabetes, graft rejection in the host, and also acute or chronic inflammatory diseases, and more generally, diseases linked to the overproduction of IL1β or TNFα cytokines.
Description of the Related Art
[0002] Active anti-cytokine immunization is an active immunotherapy strategy developed since 1990 by Zagury et al. which is based in particular on Patent Application WO 92/22577. This idea was taken up by several scientific teams which have published in international scientific journals, active immunizations against the entire IFNα protein multimerized by treatment with glutaraldehyde (Gringeri et al. , JAIDS 1999/20:358-70), a chimeric TNFα protein consisting of coupling the native TNFα protein with a T epitope of ovalbumin (Dalum et al., Nature Biotechnology, 1999;17:666-69), against entire IL9 coupled with KLH (Richard et al. , PNAS, 2000; 97:767-72) or also chimeric entire IL5 with a T epitope of tetanus toxin (Hertz- et al., J. Immunol, 2001;167:3792-99) .
[0003] These approaches have confirmed the feasibility of autologous anti-cytokine immunizations, but these few successes obscure the unsuccessful tests described by certain authors: certain cytokines do not allow sufficiently protective and clinically effective antibodies to be obtained, and the same cytokine prepared in a form which is effective in one manner, will not be effective in another (Richard et al., PNAS, 2000;97:767-72) .

[0004] In trying to explain this phenomenon, the Applicant has observed that to date all the authors have used entire cytokines (optionally slightly modified), which leads to difficulties in particular at the following levels:
dilution of the immunogenic power of the antigenic determinants of interest
possible genesis of facilitating antibodies in vivo (B response).
possible genesis of autoiinmune reaction to the potential T epitopes present in the entire cytokine (autoimmune T reaction).
[0005] This is why the Applicant has previously claimed families of peptides of limited size between 5 and 40 amino acids originating from cytokines and which have an antigenic power making it possible to generate antibodies against the native cytokine (Patent Application PCT/FR03/01120) . EP-A-0218531 also described IL1 peptides used for the preparation of antibodies. [0006] Citation of any document herein is not intended as an admission that such document is pertinent prior art, or considered material to the patentability of any claim of the present application. Any statement as to content or a date of any document is based on the information available to applicant at the time of filing and does not constitute an admission as to the correctness of such a statement.
SUMMARY OF THE INVENTION
[0007] The Applicant has evaluated certain peptides of the ILlβand TNFor cytokines with a size comprised between 10 and 3 0 residues and has demonstrated that these peptides were not only antigenic, but that they were also effective as imrnunogens for protecting in vivo against diseases linked to the overproduction of these cytokines. The present Application therefore claims peptides of a size comprised between 5 and 3 0 amino .acids, originating from murine or human IL1β and TNFα cytokines or those of any other species of mammal, and their use in humans or animals (in this case veterinary use) for preventing or treating

diseases linked to the overproduction of these cytokines. The present Application also claims the production of monoclonal or oligoclorial antibodies from these peptides and the use of these antibodies for therapeutic or preventive administration to humans or animals (veterinary application).
BRIEF DESCRIPTION OF THE DRAWINGS [0008] Figure 1 is a graph showing survival of mice immunized
against peptides and subjected to septic shock.
[0009] Figure 2 is a graph showing average clinical scores of
groups of mice immunized against peptides in a model of collagen
arthritis.
DETAILED DESCRIPTION OF THE INVENTION
[0010] The cytokine peptides according to the invention originate from or are derived from the IL1βand TNFα cytokines. By "originate" is meant that their amino acid sequence is identical to that of the cytokine. By "are derived" is meant that their amino acid sequence is mostly identical to that of the cytokine but can comprise a few differences as will be seen hereafter.
[0011] The above cytokine peptides advantageously comprise more than 5, in particular more than 7, particularly more than 9 and quite particularly more than 11 amino acids.
[0012] Under other preferential conditions for implementing the invention, the above cytokine peptides comprise less than 30, advantageously less than 25, in particular less than 20, more particularly less than 18 amino acids.
[0013] The Applicant has demonstrated that the peptide area:
[0014] 80 VSREAISYQEKVNLLS 95 (SEQ ID N0:l) of the murine TNFα cytokine makes it possible to engender antibodies by active immunization, capable of blocking TNFα -dependent septic shock in mice (Experiment 1) . The corresponding sequence of the human cytokine is 75% homologous:
80 ISRIAVSYQTKVNLLS 95 (SEQ ID NO:2)

[0015] The Applicant has also demonstrated that the peptide area:
121 YISTSQAEHKPVFLG 135 (SEQ ID NO: 3) of the murine IL1β cytokine makes it possible to engender antibodies by active immunization, capable of blocking collagen arthritis induced in mice (Experiment 2) . The corresponding sequence in humans is 8 0% homologous:
121 YISTSQAENMPVFLG 135 (SEQ ID NO: 4)
[0016] Loetascher et al. (J Biol Chem, 1993, 268:26350-357-) have shown by site specific mutagenesis experiments that the 143-147 region of TNFα could be important in the interaction with the p55 receptor of TNFα , and the present invention also claims the immunization against B epitopes of this region by means of peptides having a significant homology, be they xenogenic or mutant in relation to the human or animal cytokine sequence. The sequence corresponding to this area in humans is:
140 DYLDFAESGQVY 150 (SEQ ID NO:5) and in mice:
140 KYLDFAESGQVY 150 (SEQ ID NO: 6)
[0017] Evans et al. (J Biol Chem, 1995, 270:11477-83) have also explained by site specific mutagenesis experiments that other regions of IL1/3 could be important in the interaction with the receptor, and the present invention also claims immunization against B epitopes of these regions by means of peptides having a significant homology, be they xenogenic or mutants in relation to the targeted human or animal cytokine sequence. The sequences corresponding to this area in humans are:
3 VKSLNCTLRDSQQKSL 18 (SEQ ID NO: 7)
45 SFVQGEESNDKIP 57 (SEQ ID NO:8)
89 NYPKKKMEKRFVFNKIEI 10 6 (SEQ ID NO: 9)
143 ITDFTMQFVSS 153 (SEQ ID NO:10) and in mice:
3 IRQLHYRLRDEQQKSL 18 (SEQ ID NO:11)
45 SFVQGEPSNDKIP 57 (SEQ ID NO:12)

89 QYPKKIOffiKRFVTNKIEV 106 (SEQ ID NO: 13) 142 IIDFTMESVSS 152 (SEQ ID NO:14)
[0018] It has been possible to create autologous antibodies against the latter peptides of mice by active immunization.
[0019] Experiments 1 and 2 hereafter, carried out by the Applicant, demonstrate the therapeutic ability in vivo of the anti-peptide active immunization approach with peptides of a size less than 30 residues. The Applicant claims these peptides and their derivatives for also carrying out active immunizations allowing the generation of antibodies targeting these epitopes of the TNFα and ILlb cytokines in order to block the interaction of the cytokine-with its receptor.
[0020] As is known by a person skilled in the art of immunology, modifications of the natural peptide chains are possible without however modifying the nature of the immunological properties of the itnmunogenic peptides. Derivatives of cytokine peptides can therefore also be mentioned, which are highly homologous to these natural sequences, for example having more than 50% homology, in particular more than 7 0% homology, and preferably more than 80% homology or even more than 90% homology with the corresponding native peptide whilst retaining the immunological properties of this epitopic site of the native peptide. In particular homologous sequences of cytokines of other mammals can be used in order to obtain a xenogenic and not only an autologous protective reaction in an animal or human.
[0021] The cytokine peptide derivatives can contain modified residues, on condition that the modifications do not appreciably reduce the immunogenicity, either by adding chemical radicals
(methyl, acetyl etc.) or by stereochemical modification (use of D series amino acids). The cytokine peptide derivatives should, like the cytokine peptides induce antibodies interacting with cytokine.
[0022] The cytokine peptide derivatives according to the invention can comprise one or more modifications in the amino acids of which they are constituted, such as deletions, substitutions, additions, or functionalizations (such as

acylation) of one or more amino acids, to the extent that these modifications remain within the framework specified above (immunological characters) . For example, in general the replacement of a leucine residue by an isoleucine residue does not modify such properties; the modifications should generally concern less than 40% of the amino acids, in particular less than 30%, preferably less than 2 0% and quite particularly less then 10% of the amino acids of the natural peptide. It is important that the antibodies induced by the modified peptides are active vis-a-vis native cytokine.
[0023] These modifications are within the scope of a person skilled in the art, who can verify the incidence of the modifications by simple tests. The immunogenicity of such modified derivatives can be evaluated by ELISA after immunization of mice, the antigen tested by ELISA being the entire cytokine or the immunizing cytokine peptide, or by cytokine-receptor bond blocking tests. The possible modifications preferably affect less than 8 amino acids, advantageously less than 6 amino acids, in particular less than 4 amino acids, and particularly 3 amino acids or less, such as 2 or 1 single amino acid. [0024] A subject of the invention is also a compound characterized in that it contains at least one abovementioned cytokine peptide or cytokine peptide derivative. Such a compound can comprise identical peptide/derivative repetitions, or different peptide/derivative combinations, either in linear form or in the form of a candelabra structure or couplings mixed with carrier proteins. Such a compound can also be presented in cyclized form. Thus cytokine peptides or cytokine peptide derivatives according to the invention can for example be inserted into longer sequences of amino acids providing in particular a better conformation or combined with exogenous T epitopes (whether for protein or DNA immunizations). [0025] They can advantageously be associated in a covalent manner with carrier proteins such as for example KLH. [002 6] The cytokine peptides according to the invention, due to their limited size, correspond in general to a small number of

epitopes of the cytokine. When they are in particular inserted, combined or associated, the above compounds do not comprise other epitopes of said cytokine.
[0027] These cytokine peptides or cytokine derivatives can be included in any protein sequence which does not comprise homology with the other natural cytokine epitopes. For example, a cysteine can be added to the ends in -order to confer a cyclic structure on the peptide. Another example is a peptide surrounded by sequences of T epitopes of the tetanus toxin. Yet another example can comprise a peptide corresponding to the sequence of the receptor binding site but where certain amino acids are replaced by their D series isomers in order to avoid their agonist effect. In fact, it can be optionally advantageous to use peptide derivatives which have no agonist activity on the receptor so that the immunogen does not interfere with the immune response. [0028] In order to increase the immune response, these cytokine peptides or cytokine derivatives can be coupled to carrier proteins. The coupling methods and the carrier protein considered can be different according to the target peptide: they can for example be Keyhole Limpet Hemocyanin (KLH) protein and Tetanus Toxoid (TT) conjugated to the peptides by chemical methods well known to a person skilled in the art such as those of carbodiimide, glutaraldehyde or bis-diazotized benzidine coupling. The realization of these couplings can be facilitated by the addition or incorporation of amino acids into the sequence, such as for example lysines, histidines, tyrosines or cysteines. Such peptide compounds coupled to an exogenous T epitope (originating from plasmodium falciparumr KLH, etc*) whether chemically or genetically also come within the scope of the invention.
[0029] Network couplings of candelabra type cr to molecules such as transferrin or ferritin can also be implemented in order to effectively stimulate the immune response. [0 030] The peptides according to the invention can in particular be produced by chemical synthesis or genetic engineering or, any other suitable method. The synthesis of cyclic

[0035] The immunogenic active ingredients according to the invention can be used as follows:
[0036] A cytokine peptide or cytokine derivative or immunogenic compound according to the present invention, is administered to a patient or to an animal, for example by subcutaneous or intramuscular• route, in a sufficient quantity to be effective at a therapeutic level, to. a subject needing such treatment. The dose administered can for example range from 1 to 1000μg, in particular 10 to 500 μg, by sub-cutaneous route, once a month for three months, then periodically as a function of the induced serum antibodies count, for example every 2-6 months. In the same preparation two immunogenic molecules of the two cytokines can be administered if a still stronger blocking effect is to be obtained.
[0037] A subject of the invention is also the pharmaceutical compositions in particular the vaccines which contain at least one abovementioned cytokine peptide or cytokine derivative or immunogenic compound, as active ingredient. [003 8] As medicaments, a cytokine peptide or cytokine derivative or immunogenic compound of the invention can be incorporated into pharmaceutical compositions intended for any standard route in use in the field of vaccines, in particular by . sub-cutaneous route, by intramuscular route, by intravenous route or by oral route. The administration can take place in a single dose or repeated once or more after a certain period of time. [0039] This is why a subject of the present Application is also a curative or preventive pharmaceutical composition, characterized in that it comprises as active ingredient, one or more cytokine peptides or cytokine derivatives or immunogenic compounds, as defined above.
[0040] The immunogenic agent can be conditioned alone or mixed with an excipient or mixture of pharmaceutically acceptable excipients as an adjuvant. A subject of the present Application is more particularly a vaccine containing as immunogen, an abovementioned cytokine peptide or cytokine derivative or immunogenic compound.

[0041] A subject of the present invention is also a process for preparing a composition described above, characterized in that, according to methods known per se, the active ingredient or ingredients are mixed with acceptable, in particular pharmaceutically acceptable excipients.
[0042] The administration to a patient of a cytokine peptide or cytokine derivative or immunogenic compound according to the invention corresponds to an active immunotherapy.
[0043] It can also be useful to carry out passive immunotherapy, i.e. to provide a patient or a sick animal directly with the antibodies which they need. For this purpose, the peptides, derivatives and compounds defined previously can be used in order to produce monoclonal antibodies according to the usual techniques, :human, murine or humanized, for example by conversion of B lymphocytes from a subject immunized by the Epstein-Barr virus or by the screening of antibody libraries. These antibodies by targeting the epitopes of the above peptides block the interaction of the cytokine with its receptor and thus make it possible to reduce the pathogenic effect of the cytokine in the disease. Oligoclonal antibodies can also be prepared by active immunization in animals such as horses for example, purified, and administered therapeutically to humans or animals.
[0044] The vaccine preparations can be packaged for the intra-nasal route in the form of gel with carbopol as excipient, nasal drops or spray and for the oral route in the form of gastroresistant capsules, sugar-coated tablets or gastroresistant granules.
[0045] In the case of DNA vaccine administered by systemic or mucosal route, the galenic presentation of the plasmid can be a suspension in a physiological liquid such as physiological PBS
(phosphate buffered saline = PBS). The plasmids can be enclosed in biodegradable polymer (PLG, PLA, PCL) microspheres and administered in gastroresistant capsules for ingestion (oral route) , The DKA. can also be expressed in a bacterial, salmonella-type or viral-type, adenovirus or poxvirus living vector.

[0046] Finally, a subject of the present Application is a process for active immunization of patients characterized in that as immunogen, a cytokine peptide or cytokine derivative or immunogenic compound is used, as defined above, advantageously associated with a mineral, oily or synthetic immunity adjuvant.
[0047] The immunizations car; be done in a standard fashion in particular by peptides or immunogenic compounds as conjugates preferably in the presence of an adjuvant, for example ISA 51 or Alum. The immunizations can be DNA-based (sequences homologous to the binding sites combined with exogenous T epitopes) using naked DNA or an expression vector containing an adapted promoter such as for example pCR3.1. The DNAs administered can be protected from the nucleases by the use of appropriate radicals (CpG etc.) . In particular an initial DNA immunization can be followed by standard boosters using the peptide compounds.
[004 8] The methods of treatment of the human or animal body described in this patent can include a cytokine peptide or cytokine derivative or immunogenic compound as defined above, and can include the monoclonal or oligoclonal antibodies as defined above.
[0049] The preferential conditions for using the peptides described above also apply to the other subjects of the invention referred to above.
[0050] Figure 1 and Figure 2 show the results of protection in vivo of the immunizations described in Experiments 1 and 2 for a TNFα peptide in TNFα -dependent septic shock and an ILIΒ peptide in collagen arthritis.
[0051] The experiments which follow illustrate the present invention.
Experiment 1:
[0052] 4 murine TNFα peptides coupled to the KLH carrier protein, including the cyclized peptide CVSRFAISYQEKVNLLSC (SEQ ID NO:15) called TNFα -6, were tested in a model of endotoxinic shock. For this purpose, Balb/c mice were preimrmmizad against these peptides on days DO, D8, D16, and D4 0. On day D50, the mice

were subjected to shock, i.e. they were injected with LPS with Galactosamine. A control was carried out on mice immunized against KLH alone.
[0053] It is noted that all the mice died after two days, except for the group immunized against the TNFα-6 peptide where the mice were protected. The protection conferred by the immunization was very significant (p =. 0.008).
Experiment 2:
[0054] 3 jnurine IL1β peptides coupled to the KLH protein, including the cyclized IL1β-6 peptide of sequence YCYISTSQAEHKPVFLGC (SEQ ID NO:16), were tested in a' model of collagen arthritis. For this purpose, DBA1 mice were preimmunized against these peptides on days DO, D20, D40, D60. On day D80 the mice were immunized against collagen in Freund's adjuvant, and similarly on day D95. The development of arthritis was monitored between day D100 and day D160: twice weekly, the mice were examined and a score was attributed to them as a function of the: state of inflammation of their joints (0 = no inflammation, 1 = slight inflammation, 2 = average inflammation, 3 = strong inflammation).
[0055] It is noted that the control mice immunized by KLH alone exhibit strong inflammation (curve with squares) whereas the group of mice immunized against the IL1β-6 peptides (curve with diamonds) exhibit a strong protection level with respect to the control (p = 0.0003, ANOVA test)..
Experiment 3
[0 056] 6 groups of 4 mice were immunized against 2 0 ug of the murine IL1β peptides IRQLHYRLRDEQQKSL (group 1) (SEQ ID NO:11), SFVQGEPSNDKIP (group 2) (SEQ ID NO: 12), QYPKKKMEKRFVFNKIEV (group 3) (SEQ ID N0:13), IIDFTMESVSS (group 4) (SEQ ID NO:14), and 20 ug of the murine TNFα peptide KYLDFAESGQVY (group 5) (SEQ ID NO: 6) all coupled to KLH. Group 6 corresponds to mice immunized by KLH alone. A booster was administered on days D20 and D40 . On day D50 the mice were sacrificed and the antibodies directed

against the native mTNFo: cytokine and the native mILlβ cytokine in the serums were measured by an ELISA test.
[0057] The averages obtained for each group are indicated in the table hereafter.

[0058] It is therefore clear that these peptides are well capable of inducing antibodies recognizing the native cytokine. These antibodies are very specific since they recognize only the cytokine the sequence of which was used for the immunization.







WHAT IS CLAIMED IS:
1. A peptide originating from mammalian IL1β or TNFα
cytokines, homologous to one of the following peptides of human
ILlβ or TNFα cytokines:
80 ISRIAVSYQTKVNLLS 95 (SEQ ID NO:2)
140 DYLDFAESGQVY 150 (SEQ ID NO:5)
3 VKSLNCTLRDSQQKSL 18 (SEQ ID NO:7)
45 SFVQGEESNDKIP 57 (SEQ ID NO:8)
89 NYPKXKMEKRFVFNKIEI 10 6 (SEQ ID NO: 9)
121 YISTSQAENMPVFLG 135 (SEQ ID NO:4)
143 ITDFTMQFVSS 153 (SEQ ID NO:10)
2. A peptide according to claim 1 , wherein the human
3. TNFα cytokine peptide sequence is ISRIAVSYQTKVNLLS (SEQ ID NO:2)
4. A peptide according to claim 1, wherein the human
5. TNFα cytokine peptide sequence is DYLDFAESGQVY (SEQ ID NO: 5)
6. A peptide according to claim 1, wherein the human
7. IL1β cytokine peptide sequence is VKSLNCTLRDSQQKSL (SEQ ID NO: 7) .
8. A peptide according to claim 1, wherein the- human
9. IL1β cytokine peptide sequence is SFVQGEESNDKIP (SEQ ID NO: 8).
10. A peptide according to claim 1, wherein the human
11. IL1β cytokine peptide sequence is NYPKKKMEKRFVFNKIEI (SEQ ID
12. NO:9).
13. A peptide according to claim 1, wherein the human
14. IL1β cytokine peptide sequence is YISTSQAENMPVFLG (SEQ ID NO: 4) .
15. A peptide according to claim 1, wherein the human
16. IL1/? cytokine sequence is ITDFTMQFVSS (SEQ ID NO: 10) .

10. A derivative of the peptide according to any of
11. claims 1 to 9.
12. A peptide according to one of claims 1 to 10
13. characterized in that it consists of less than 30 amino acids.
14. A derivative of a peptide as defined in any one of
15. claims 1 to 11 by deletion, substitution, addition, cyclization,

stereochemical modification (use of D series amino acids) or functionalization (such as acylation) of one or more amino acids of said peptide.
13. An immunogenic compound characterized in that it
14. comprises a peptide or peptide derivative as defined in any one of
15. claims 1 to 12, it being understood that it comprises no other
16. epitopes of said cytokine and in that it is capable of generating
17. in a subject antibodies recognizing the native cytokine.
18. A peptide or peptide derivative or immunogenic
19. compound as defined in any one of claims 1 to 13 for use in a
20. method for preventive or therapeutic treatment of the human body.
21. A peptide or peptide derivative or immunogenic
22. compound as defined in any one of claims 1 to 13 for use in a
23. method for preventive or therapeutic treatment of the animal body
(veterinary) .
16. Use of a peptide or peptide derivative or
immunogenic compound as defined in any one of claims 1 to 15 for
the preparation of a curative or preventive medicament intended
for the treatment or prevention of diseases linked to the
presence or excess of cytokines.
17. A pharmaceutical composition which contains at least
one peptide or peptide derivative or immunogenic compound as
defined in any one of claims 1 to 15 as active ingredient.
18. Monoclonal or oligoclonal antibody specific to a
peptide defined in any one of claims 1 to 15.
19. Use of the antibodies as defined in claim 18 for the
20. preventive or therapeutic treatment of the human or animal body.
21. A method for the treatment of a disease associated
22. with the pathogenic overproduction of I L1β or TNFα, comprising
23. administering to a patient in need thereof an antibody as defined
24. in claim 18 to treat the disease associated with the pathogenic
25. overproduction of ILlβ or TNFα.

21. A method for the treatment or prevention of diseases associated with the pathogenic overproduction of ILlβ or TNPα, comprising administering to a patient in need thereof a peptide or peptide derivative or immunogenic compound as defined in any one of claims 1 to 15 to treat or inhibit the disease associated with the pathogenic overproduction of IL1β or TNFα.


Documents:

3110-CHENP-2006 AMENDED CLAIMS 13-05-2011.pdf

3110-CHENP-2006 AMENDED PAGES OF SPECIFICATION 13-05-2011.pdf

3110-chenp-2006 form-1 25-05-2011.pdf

3110-chenp-2006 form-13 25-05-2011.pdf

3110-CHENP-2006 FORM-2 25-05-2011.pdf

3110-CHENP-2006 OTHER PATENT DOCUMENT 13-05-2011.pdf

3110-chenp-2006 other patent document 25-05-2011.pdf

3110-CHENP-2006 CORRESPONDENCE OTHERS 25-05-2011.pdf

3110-chenp-2006 form-3 25-05-2011.pdf

3110-CHENP-2006 POWER OF ATTORNEY 25-05-2011.pdf

3110-CHENP-2006 ABSTRACT.pdf

3110-CHENP-2006 CLAIMS.pdf

3110-CHENP-2006 CORRESPONDENCE OTHERS 17-08-2010.pdf

3110-CHENP-2006 DESCRIPTION (COMPLETE).pdf

3110-CHENP-2006 DRAWINGS.pdf

3110-CHENP-2006 EXAMINATION REPORT REPLY RECEIVED 13-05-2011.pdf

3110-CHENP-2006 FORM-18.pdf

3110-CHENP-2006 CORRESPONDENCE OTHERS.pdf

3110-CHENP-2006 FORM 18.pdf

3110-chenp-2006-abstract.pdf

3110-chenp-2006-claims.pdf

3110-chenp-2006-correspondnece-others.pdf

3110-chenp-2006-description(complete).pdf

3110-chenp-2006-drawings.pdf

3110-chenp-2006-form 1.pdf

3110-chenp-2006-form 3.pdf

3110-chenp-2006-form 5.pdf

3110-chenp-2006-pct.pdf

3110-chenp-2006-sequence listing.pdf


Patent Number 247832
Indian Patent Application Number 3110/CHENP/2006
PG Journal Number 21/2011
Publication Date 27-May-2011
Grant Date 25-May-2011
Date of Filing 25-Aug-2006
Name of Patentee VAXCONSULTING
Applicant Address VAXCONSULTING., c/o ZAGURY, 117, rue Vieille du Temple, F-75003 Paris
Inventors:
# Inventor's Name Inventor's Address
1 ZAGURY, Jean-Francois ZAGURY, Jean-Francois., c/o ZAGURY, 117, rue Vieille du Temple, F-75003 Paris
2 BOISSIER, Marie-Christophe 41, rue Madame, F-75006 Paris
3 BESSIS, Natacha 73, Bld Voltaire, F-75011 Paris
PCT International Classification Number A61K38/08,C07K14/00
PCT International Application Number PCT/US2005/005890
PCT International Filing date 2005-02-25
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/547,848 2004-02-27 U.S.A.