| CPC C07K 16/2803 (2013.01) [A61K 38/17 (2013.01); A61K 39/395 (2013.01); A61K 39/3955 (2013.01); A61K 45/06 (2013.01); A61P 1/00 (2018.01); A61P 1/16 (2018.01); A61P 13/12 (2018.01); A61P 17/06 (2018.01); A61P 19/02 (2018.01); A61P 37/06 (2018.01); C07K 16/2827 (2013.01); C07K 16/2896 (2013.01); A61K 2039/505 (2013.01); C07K 2317/21 (2013.01); C07K 2317/24 (2013.01); C07K 2317/31 (2013.01); C07K 2317/33 (2013.01); C07K 2317/34 (2013.01); C07K 2317/52 (2013.01); C07K 2317/522 (2013.01); C07K 2317/53 (2013.01); C07K 2317/565 (2013.01); C07K 2317/73 (2013.01); C07K 2317/74 (2013.01); C07K 2317/75 (2013.01); C07K 2317/76 (2013.01); C07K 2317/92 (2013.01)] | 14 Claims |
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1. A method of treating lupus comprising administering to a patient in need thereof a therapeutically effective amount of an isolated antibody comprising an antigen binding region that specifically binds to human V-domain Ig Suppressor of T cell Activation (human VISTA), wherein the antibody agonizes or promotes the effects of VISTA on T cell immunity, and further wherein the antibody comprises a variable heavy chain which comprises heavy chain CDR1, CDR2 and CDR3 polypeptides having the sequences of SEQ ID NO: 740, 741 and 742 respectively and further comprises a variable light chain which comprises the light chain CDR1, CDR2 and CDR3 polypeptides having the sequences of SEQ ID NO: 743, 744 and 745 respectively, and wherein the antibody comprises a full length human IgG2 Fc region that comprises native binding to human Fc gamma receptors.
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