CPC C07K 16/2803 (2013.01) [A61N 5/10 (2013.01); A61P 35/00 (2018.01); C07K 16/2818 (2013.01); C07K 16/2827 (2013.01); G01N 33/57415 (2013.01); G01N 33/57423 (2013.01); A61K 2039/505 (2013.01); A61K 2039/507 (2013.01); C07K 2317/565 (2013.01); C07K 2317/73 (2013.01); C07K 2317/76 (2013.01); C07K 2317/92 (2013.01); G01N 2333/70532 (2013.01)] | 20 Claims |
1. A method of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a molecule comprising an antigen binding fragment that immunospecifically binds to BTN1A1, wherein the cancer expresses PD-L1 at a level lower than or equal to a PD-L1 reference level; wherein the PD-L1 reference level is the average or medium expression level of PD-L1 in a population of healthy individuals; and wherein the antigen binding fragment comprises:
(i) a heavy chain variable region (VH) comprising a VH complementarity-determining region (CDR) 1, a VH CDR2, and a VH CDR3 having an amino acid sequence of a VH CDR1, a VH CDR2, and a VH CDR3, respectively, of a VH having an amino acid sequence of SEQ ID NO:31; and
(ii) a light chain variable region (VL) comprising a VL CDR1, a VL CDR2, and a VL CDR3 having an amino acid sequence of a VL CDR1, a VL CDR2, and a VL CDR3, respectively, of a VL having an amino acid sequence of SEQ ID NO:33.
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