Antibodies to tigit
AssigneeArcus Biosciences, Inc.
InventorsKelsey Sivick GAUTHIER, Nigel Pelham Clinton WALKER, Xiaoning ZHAO, John LIPPINCOTT
Life of this patent
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Abstract
The present disclosure provides antibodies that specifically bind to TIGIT. The antibodies have the capacity for substantial activation of T cells and natural killer cells by inhibiting binding of TIGIT to CD155. The antibodies can be used for treatment of cancer and infectious disease, among other applications.
Claims25
An anti-TIGIT antibody or antigen-binding fragment thereof that specifically binds to human TIGIT, comprising
- (a) a heavy chain variable region comprising a heavy chain (HC) complementarity determining region (CDR) 1 having at least 80% sequence identity to SEQ ID NO:
- 36, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 37, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 38;
- and a light chain variable region comprising a light chain (LC) CDR1 having at least 80% sequence identity to SEQ ID NO:
- 39, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 40, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 41;
- (b) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 42, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 43, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 44;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 45, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 46, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 47;
- (c) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 48, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 49, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 50;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 51, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 52, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 53;
- (d) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 54, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 55, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 56;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 57, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 58, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 59;
- (e) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 60, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 61, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 62;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 63, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 64, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 65;
- (f) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 60, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 66, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 67;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 63, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 68, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 65;
- (g) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 69, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 55, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 70;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 71, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 68, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 65;
- (h) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 72, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 73, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 67;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 63, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 68, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 65;
- or
- (i) a heavy chain variable region comprising an HC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 74, an HC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 75, and an HC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 67;
- and a light chain variable region comprising an LC-CDR1 having at least 80% sequence identity to SEQ ID NO:
- 63, an LC-CDR2 having at least 80% sequence identity to SEQ ID NO:
- 68, and an LC-CDR3 having at least 80% sequence identity to SEQ ID NO:
- 65.
(canceled)
13-14. (canceled)
(canceled)
An anti-TIGIT antibody or antigen-binding fragment thereof that specifically binds to human TIGIT, comprising a heavy chain having an amino acid sequence comprising SEQ ID NO:
- 92 and a light chain having an amino acid sequence comprising SEQ ID NO:
- 93.
22-34. (canceled)
An anti-TIGIT antibody or antigen binding fragment thereof that binds to an epitope of human TIGIT comprising at least one of the following amino acid residues of SEQ ID NO 80:
- T55, Q56, N58, E60, D72, S80, and K82.
37-39. (canceled)
Dependencies are inferred from the claim text.