IP Library Granted Patent US 10,005,845
Granted Patent B2
US 10,005,845 · App. 14/442,320 · Granted Jun 26, 2018

Antibodies and fragments thereof raised against the alpha-3 domain of HLA-G protein, methods and means for their preparation, and uses thereof

Inventors: Maria de las Nieves Loustau (Paris, FR); Julien Caumartin (Le Vesinet, FR); Pierre Langlade-Demoyen (Neuilly sur Seine, FR)
Assignee: INVECTYS
C07K16/34A61K39/0005C07K14/70539C07K16/2833A61K2039/53A61K2039/585C07K2317/24C07K2317/76
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Quick Facts
Patent No.
US 10,005,845
App. No.
14/442,320
Granted
Jun 26, 2018
Kind
B2
Abstract

An antibody or antigen-binding fragment thereof which specifically binds the α3 domain of a HLA-G protein, in particular binds the β2-microglobulin free HLA-G protein exhibiting an α3 domain. The nucleic acid molecules encoding a human HLA-G α3 domain polypeptide, which is selected from a group of specific sequences, and vectors for the cloning and/or expression of such nucleic acid molecules, recombined cells or cell lines and compositions for use in a host in need thereof to interfere with and neutralize the immune down-regulation due to HLA-G proteins, and/or improving or treating conditions showing HLA-G+ lesions, and/or improving or treating a neoplasic condition or disease. A method of producing the antibody or antigen-binding fragment thereof, immunogenic compositions for use to elicit in a host an immune response against the α3 domain of HLA-G protein, and an in vitro method for detecting HLA-G protein in a sample are also described.

Claims (18)

1. A method of producing an antibody or an antigen-binding fragment thereof which specifically binds the α3 domain of a HLA-G protein, the method comprising administering to a mammal a nucleic acid molecule encoding a polypeptide comprising the amino-acid sequence of SEQ ID NO: 1, or an amino-acid sequence comprising at least 99% amino acid identity over the entirety of SEQ ID NO: 1.

2. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof which specifically binds the α3 domain of a HLA-G protein is a blocking antibody or antigen-binding fragment thereof.

3. The method according to claim 1 , further comprising recovering antibodies elicited by said mammal from sera or plasma obtained from said mammal.

4. The method of claim 3 , further comprising preparing antigen-binding fragments from the recovered antibodies.

5. The method according to claim 3 , further comprising checking the recovered antibodies for specificity to the α3 domain of the HLA-G protein.

6. The method according to claim 3 , further comprising preparing antigen-binding fragments from the recovered antibodies.

7. The method according to claim 1 , wherein the mammal is a non-human mammal.

8. The method according to claim 1 , wherein said antibody or antigen-binding fragment binds the α3 domain of a HLA-G protein when the α3 domain is in a monomeric and/or a dimeric form.

9. The method according to claim 1 , wherein said antibody or antigen-binding fragment binds the α3 domain when present in the HLA-G protein.

10. The method according to claim 1 , wherein said antibody or antigen-binding fragment binds the α3 domain when present in a β2-microglobulin free HLA-G protein or HLA-G protein isoform.

11. The method according to claim 1 , wherein said antibody or antigen-binding fragment does not bind the α3 domain when the HLA-G protein is associated with the β2-microglobulin.

12. The method according to claim 1 , wherein said antibody or antigen-binding fragment blocks binding of a HLA-G protein to at least one of LILRB1 and LILRB2 receptors.

13. The method according to claim 1 , wherein said nucleic acid molecule comprises the nucleic acid sequence of SEQ ID NO: 9, SEQ ID NO: 10, or SEQ ID NO: 6.

14. The method according to claim 1 , wherein said nucleic acid molecule is administered to the mammal in the form of naked DNA.

15. The method according to claim 1 , wherein said nucleic acid molecule is administered to the mammal by a delivery method selected from the group consisting of intramuscular or intradermal injection, electroporation, gene-gun delivery, needle-free delivery system, topical administration, and a combination thereof.

16. The method according to claim 1 , further comprising administering an adjuvant to the mammal.

17. The method according to claim 1 , wherein the nucleic acid molecule encodes a polypeptide comprising the amino-acid sequence of SEQ ID NO: 2.

18. The method according to claim 1 , wherein the nucleic acid molecule encodes a polypeptide comprising the amino-acid sequence of SEQ ID NO: 1.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 13, 2015
From: LOUSTAU, MARIA DE LAS NIEVES; CAUMARTIN, JULIEN; LANGLADE-DEMOYEN, PIERRE
To: INVECTYS
Reel/Frame 036319/0543 →
Priority Claims (1)
EP 12306398 · Nov 12, 2012 · regional
Continuity (1)
Related Publication 20160272724A1 · Sep 22, 2016
Cited By (2)
US 12,269,861 US 12,344,670