CPC C07K 16/2818 (2013.01) [A61P 35/00 (2018.01); C07K 16/2878 (2013.01); A61K 2039/505 (2013.01); C07K 2317/21 (2013.01); C07K 2317/24 (2013.01); C07K 2317/33 (2013.01); C07K 2317/51 (2013.01); C07K 2317/52 (2013.01); C07K 2317/565 (2013.01); C07K 2317/70 (2013.01); C07K 2317/72 (2013.01); C07K 2317/732 (2013.01); C07K 2317/76 (2013.01); C07K 2317/92 (2013.01); C07K 2317/94 (2013.01)] | 20 Claims |
1. A method of treating a disorder in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising an isolated monoclonal antibody or an antigen-binding portion thereof comprising a CD152-binding domain, and a pharmaceutical acceptable excipient,
wherein the CD152-binding domain comprises an immunoglobulin heavy chain variable region comprising CDR1, CDR2, and CDR3,
wherein the CDR1, CDR2, and CDR3 comprise amino acid sequences of
(1) SEQ ID NOs: 4, 5 and 6, respectively;
(2) SEQ ID NOs: 10, 11 and 12, respectively;
(3) SEQ ID NOs: 16, 17 and 18, respectively;
(4) SEQ ID NOs: 22, 23 and 24, respectively;
(5) SEQ ID NOs: 28, 29 and 30, respectively;
(6) SEQ ID NOs: 34, 35 and 36, respectively;
(7) SEQ ID NOs: 40, 41 and 42, respectively;
(8) SEQ ID NOs: 46, 47 and 48, respectively;
(9) SEQ ID NOs: 52, 53 and 54, respectively;
(10) SEQ ID NOs: 58, 59 and 60, respectively;
(11) SEQ ID NOs: 64, 65 and 66, respectively;
(12) SEQ ID NOs: 94, 95 and 96, respectively;
(13) SEQ ID NOs: 100, 101 and 102, respectively; or
(14) SEQ ID NOs: 184, 185 and 186, respectively; and
wherein the disorder is a cancer or an autoimmune disease.
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