US2024002514A1PendingUtilityA1

Anti-pd-l1 antibodies

Assignee: IGM BIOSCIENCES INCPriority: May 9, 2016Filed: Sep 7, 2023Published: Jan 4, 2024
Est. expiryMay 9, 2036(~9.8 yrs left)· nominal 20-yr term from priority
C07K 16/2827C07K 16/30G01N 33/6854C07K 2317/21C07K 2317/24C07K 2317/31C07K 2317/33C07K 2317/34C07K 2317/622C07K 16/20C07K 2317/52C07K 2317/76C07K 2317/92A61P 35/00A61P 35/02A61P 43/00G01N 2333/70532
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Claims

Abstract

Aspects of the invention include isolated anti-PD-L1 antibodies, as well as compositions containing such antibodies, and methods of using the same in the treatment of diseases or conditions that are mediated by PD-L1 signaling.

Claims

exact text as granted — not AI-modified
1 . A polynucleotide encoding a heavy chain or a light chain of an anti-PD-L1 antibody or antigen-binding fragment thereof, wherein the heavy chain comprises a heavy chain variable region (VH) having at least 90% sequence identity to SEQ ID NO:37 or SEQ ID NO:45, wherein the light chain comprises a light chain variable region (VL) having at least 90% sequence identity to SEQ ID NO:46, and wherein the antibody or antigen-binding fragment thereof comprises:
 (i) an HVR-L1 comprising the sequence of RASQDISIWLS (SEQ ID NO:1);   (ii) an HVR-L2 comprising the sequence of KASNLHT (SEQ ID NO:2);   (iii) an HVR-L3 comprising the sequence of LQSQSFPRT (SEQ ID NO:3);   (iv) an HVR-H1 comprising the sequence of GFSLTSYDIS (SEQ ID NO:4);   (v) an HVR-H2 comprising the sequence of VIWTGVGTN (SEQ ID NO:5); and   (vi) an HVR-H3 comprising the sequence of DPYYYGMDY (SEQ ID NO:6).   
     
     
         2 . The polynucleotide of  claim 1 , wherein the VH comprises the amino acid sequence SEQ ID NO45. 
     
     
         3 . The polynucleotide of  claim 2 , wherein the VL comprises the amino acid sequence SEQ ID NO46. 
     
     
         4 . The polynucleotide of  claim 1 , wherein the VH comprises the amino acid sequence SEQ ID NO:37. 
     
     
         5 . The polynucleotide of  claim 4 , wherein the VL comprises the amino acid sequence SEQ ID NO44. 
     
     
         6 . The polynucleotide of  claim 1 , wherein the antibody is an IgA isotype. 
     
     
         7 . The polynucleotide of  claim 1 , wherein the antibody is an IgG isotype. 
     
     
         8 . The polynucleotide of  claim 1 , wherein the antibody is an IgM isotype. 
     
     
         9 . A vector comprising a promoter operably linked to the polynucleotide of  claim 1 , wherein the vector encodes the heavy chain and the light chain. 
     
     
         10 . A host cell comprising a first polynucleotide encoding a heavy chain of an anti-PD-L1 antibody and a second polynucleotide encoding a light chain of the anti-PD-L1 antibody, wherein the coding sequences are operably linked to a promoter, wherein the VL comprises three complementarity determining regions (CDRs), such that
 (i) VL CDR1 comprises the sequence of SEQ ID NO: 1;   (ii) VL CDR2 comprises the sequence of SEQ ID NO:2; and   (iii) VL CDR3 comprise the sequence of SEQ ID NO:3;   
       and wherein the VH comprises three CDRs, such that
 (iv) VH CDR1 comprises the sequence of SEQ ID NO:4; 
 (v) VH CDR2 comprises the sequence of SEQ ID NO:5, and 
 (vi) VH CDR3 comprises the sequence of SEQ ID NO:6. 
 
     
     
         11 . A method of producing an anti-PD-L1 antibody, or an antigen-binding fragment thereof, comprising: (a) culturing the host cell of  claim 10 ; and (b) isolating the anti-PD-L1 antibody or the antigen-binding fragment thereof from the culture. 
     
     
         12 . The method of  claim 11 , wherein the first polynucleotide encodes a VH having at least 90% sequence identity to SEQ ID NO: 45 and the second polynucleotide encodes a VL having at least 90% sequence identity to SEQ ID NO: 46. 
     
     
         13 . The method of  claim 12 , wherein the VH comprises the amino acid sequence SEQ ID NO: 45 and the VL comprises the amino acid sequence SEQ ID NO: 46. 
     
     
         14 . The method of  claim 11 , wherein the anti-PD-L1 antibody thereof is a chimeric antibody or a humanized antibody. 
     
     
         15 . The method of  claim 11 , wherein: the first polynucleotide encodes a VH having at least 90% sequence identity to the sequence of any one of SEQ ID NOS: 36, 37, 38, 39, 40, 41, or 42; and wherein the second polynucleotide encodes a VL having at least 90% sequence identity to any one of SEQ ID NOS: 43 or 44. 
     
     
         16 . The method of  claim 15 , wherein the first polynucleotide encodes SEQ ID NO: 36, 37, 38, 39, 40, 41, or 42 and the second polynucleotide encodes SEQ ID NO: 43 or 44. 
     
     
         17 . The method of  claim 11 , wherein the anti-PD-L1 antibody or the antigen-binding fragment thereof is bispecific. 
     
     
         18 . The method of  claim 17 , wherein the bispecific antibody or antigen-binding fragment binds to a PD-L1 protein and a cell surface protein. 
     
     
         19 . The method of  claim 18 , wherein the cell surface protein is selected from the group consisting of: CD20, EGFR, HER2, CTLA-4, TIM3, LAG3, VISTA and TIGIT. 
     
     
         20 . The method of  claim 11 , wherein the antigen-binding fragment is selected from the group consisting of: Fab, Fab′, F(ab) 2 , F(ab′) 2 , Fv, and scFv. 
     
     
         21 . The method of  claim 11 , wherein the antibody is an IgG, IgM, IgA, IgD, or IgE isotype. 
     
     
         22 . The method of  claim 21 , wherein the antibody is an IgM isotype. 
     
     
         23 . The method of  claim 22 , wherein the antibody comprises a J-chain. 
     
     
         24 . The method of  claim 21 , wherein the antibody is an IgA isotype, wherein the antibody is a subclass selected from the group consisting of: IgA1 and IgA2, and wherein the antibody comprises a J-chain. 
     
     
         25 . The method of  claim 23 , wherein the J-chain is a modified J-chain comprising an extraneous binding moiety. 
     
     
         26 . The method of  claim 11 , wherein the anti-PD-L1 antibody or the antigen-binding fragment thereof is a PD-L1 antagonist. 
     
     
         27 . The method of  claim 16 , wherein the VH comprises the amino acid sequence SEQ ID NO: 37 and the VL comprises the amino acid sequence SEQ ID NO: 44. 
     
     
         28 . The method of  claim 11 , further comprising: (c) transfecting the host cell with a composition comprising the first and the second polynucleotides. 
     
     
         29 . The method of  claim 28 , where the composition further comprises a third polynucleotide encoding a J-chain. 
     
     
         30 . The method of  claim 29 , wherein the J-chain is a modified J-chain comprising an extraneous binding moiety.

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