IP Library › Granted Patent US 11,634,494
Granted Patent B2
US 11,634,494 · App. 17/728,483 · Granted Apr 25, 2023

Anti HLA-G specific antibodies

Inventors: Pierre Langlade Demoyen (Neuilly-sur-Seine, FR); Thierry Huet (Nogent sur Marne, FR); Julien Caumartin (Le Vésinet, FR); Maria Loustau (Paris, FR); Maria Wehbe (Montigny-le-Bretonneux, FR)
Assignee: Invectys SA
C07K16/2833A61P31/12A61P35/00C07K7/08C07K7/50C07K2317/33C07K2317/34C07K2317/622C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 11,634,494
App. No.
17/728,483
Granted
Apr 25, 2023
Kind
B2
Abstract

The present invention relates to antibodies, or antigen-binding fragments thereof, directed against human leukocyte antigen-G (HLA-G) protein and raised against an immunogenic peptide derived from the α3 domain of HLA-G protein. The invention further relates to the immunogenic peptide, and methods for producing said anti-HLA-G specific antibodies.

Claims (12)

1. A pharmaceutical composition comprising an anti-human leukocyte antigen G (HLA-G) antibody or an antigen-binding fragment thereof, and a pharmaceutical carrier;

wherein the antibody or antigen-binding fragment comprises:

(a) a heavy chain variable region (VH) comprising a heavy chain complementarity determining region 1 (HC CDR1) of SEQ ID NO: 8, a heavy chain complementarity determining region 2 (HC CDR2) of SEQ ID NO: 10, and a heavy chain complementarity determining region 3 (HC CDR3) of SEQ ID NO: 12; and

(b) a light chain variable region (VL) comprising a light chain complementarity determining region 1 (LC CDR1) of SEQ ID NO: 2, a light chain complementarity determining region 2 (LC CDR2) of sequence KVS and a light chain complementarity determining region 3 (LC CDR3) of SEQ ID NO: 5.

2. The pharmaceutical composition of claim 1 , wherein the VH comprises SEQ ID NO: 64 and the VL comprises SEQ ID NO: 63.

3. The pharmaceutical composition of claim 2 , wherein the antibody is a full-length immunoglobulin G comprising two heavy chains and two light chains.

4. The pharmaceutical composition of claim 1 , wherein the antibody or antigen-binding fragment is humanized or chimeric.

5. The pharmaceutical composition of claim 1 , wherein the VH, the VL, or both the VH and VL comprise human immunoglobulin framework region sequences.

6. The pharmaceutical composition of claim 1 , wherein the antibody comprises an immunoglobulin constant region.

7. The pharmaceutical composition of claim 1 , wherein the antigen-binding fragment is a Fv, a dsFv, a scFv, a Fab, a Fab′, or a F(ab′) 2 .

8. The pharmaceutical composition of claim 1 , wherein the antibody is monoclonal.

9. The pharmaceutical composition of claim 1 , wherein the antibody or antigen-binding fragment is linked to a cytotoxic agent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2022
From: LANGLADE DEMOYEN, PIERRE; HUET, THIERRY; CAUMARTIN, JULIEN; LOUSTAU, MARIA; WEHBE, MARIA
To: INVECTYS SA
Reel/Frame 059773/0865 →
Priority Claims (1)
EP 16305650 · Jun 3, 2016 · regional
Continuity (4)
Continuation 17466607 · Sep 3, 2021
Continuation 17080017 · Oct 26, 2020
Continuation 16306267
Related Publication 20220251216A1 · Aug 11, 2022