US2023295295A1PendingUtilityA1
Antigen binding proteins
Assignee: GLAXOSMITHKLINE IP DEV LTDPriority: Mar 15, 2013Filed: Jan 19, 2023Published: Sep 21, 2023
Est. expiryMar 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
C07K 16/2803C07K 2317/56C07K 2317/565C07K 2317/732C07K 2317/92A61P 1/00A61P 1/04A61P 1/16A61P 17/06A61P 19/02A61P 25/00A61P 29/00A61P 31/00A61P 35/00A61P 37/00A61P 37/02A61P 37/04A61P 37/06A61P 37/08A61P 43/00A61K 39/39541A61K 39/39558C07K 2317/24
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Claims
Abstract
This application discloses antigen binding proteins that bind Lymphocyte Activation Gene 3 (LAG-3), and more particularly to antigen binding proteins that cause depletion of LAG-3+ activated T cells.
Claims
exact text as granted — not AI-modified1 . An isolated nucleic acid molecule which encodes an antigen binding protein which is capable of binding Lymphocyte Activating Gene 3 (LAG-3) and which comprises
CDRL1 comprising SEQ ID NO: 1; CDRL2 comprising SEQ ID NO: 2; CDRL3 comprising SEQ ID NO: 3; CDRH1 comprising SEQ ID NO: 6; CDRH2 comprising SEQ ID NO: 7; and CDRH3 comprising SEQ ID NO: 8.
2 . An isolated nucleic acid molecule according to claim 1 , wherein the antigen binding protein encoded by the isolated nucleic acid molecule is a humanised antibody, wherein the humanised antibody comprises an IgG1 constant region.
3 . An expression vector comprising a nucleic acid molecule according to claim 1 .
4 . An expression vector comprising a nucleic acid molecule according to claim 2 .
5 . A host cell comprising an expression vector according to claim 2 .
6 . A host cell comprising an expression vector according to claim 4 .
7 . A host cell comprising an expression vector according to claim 3 , wherein FUT8 gene encoding alpha-1,6-fucosyltransferase has been inactivated in the host cell.
8 . A host cell comprising an expression vector according to claim 4 , wherein FUT8 gene encoding alpha-1,6-fucosyltransferase has been inactivated in the host cell.
9 . A method of producing an antigen binding protein comprising a) culturing a host cell according to claim 5 and b) isolating the antigen binding protein.
10 . A method of producing an antigen binding protein comprising a) culturing a host cell according to claim 7 and b) isolating the antigen binding protein.
11 . A method of treatment of a human or animal subject comprising administering to the human or animal subject an antigen binding protein which is capable of binding Lymphocyte Activating Gene 3 (LAG-3) and which comprises
CDRL1 comprising SEQ ID NO: 1; CDRL2 comprising SEQ ID NO: 2; CDRL3 comprising SEQ ID NO: 3; CDRH1 comprising SEQ ID NO: 6; CDRH2 comprising SEQ ID NO: 7; and CDRH3 comprising SEQ ID NO: 8.
12 . A method of treatment according to claim 11 , wherein the disease is associated with the involvement of pathogenic T cells in the human or animal subject.
13 . A method of treatment according to claim 12 , wherein the disease is an autoimmune disease or cancer.
14 . A method of treatment according to claim 13 , wherein the disease is an autoimmune disease and the autoimmune disease is selected from the group consisting of psoriasis, Crohn’s disease, rheumatoid arthritis, primary biliary cirrhosis, SLE, Sjogren’s syndrome, multiple sclerosis, ulcerative colitis, and autoimmune hepatitis.
15 . A method of producing an antigen binding protein, comprising a) culturing a host cell according to claim 6 , and b) isolating the antigen binding protein.
16 . A method of producing an antigen binding protein comprising a) culturing a host cell according to claim 8 , and b) isolating the antigen binding protein.Join the waitlist — get patent alerts
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