Treatment of cancer with anti-LAP monoclonal antibodies
Described herein are compositions and methods relating to LAP-binding agents, including, for example, anti-LAP antibodies, and to their use in methods of treatment of cancer. LAP-binding agents affected both systemic and intra-tumor immunity and were shown effective to treat a broad spectrum of cancer types.
1. A humanized form of an antibody that binds latency-associated peptide, the antibody comprising the heavy chain complementarity determining regions CDR1, CDR2, and CDR3 and the light chain complementarity determining regions CDR1, CDR2, and CDR3 of the antibody produced by the hybridoma designated TW7-28G11 (ATCC Accession No. PTA-124319), or an antigen binding fragment thereof.
2. The humanized antibody, or antigen-binding fragment thereof, of claim 1 , wherein the antibody produced by TW7-28G11 comprises heavy chain complementarity determining region CDR1, CDR2, and CDR3 sequences set forth in SEQ ID NOs: 9, 10, and 11, respectively, and light chain complementarity determining region CDR1, CDR2, and CDR3 sequences set forth in SEQ ID NOs: 14, 15, and 16, respectively.
3. The humanized antibody, or antigen-binding fragment thereof, of claim 1 , which comprises a human acceptor framework.
4. The humanized antibody, or antigen-binding fragment thereof, of claim 1 , which comprises a human light chain variable kappa framework region.
5. The humanized antibody, or antigen-binding fragment thereof, of claim 1 , which comprises a human light chain variable lambda framework region.
6. The humanized antibody, or antigen-binding fragment thereof, of claim 1 , which comprises a human constant region selected from the group consisting of IgG, IgE, IgM, IgD, IgA, and IgY.
7. The humanized antibody, or antigen-binding fragment thereof, of claim 1 , which comprises a human IgG constant region.
8. The humanized antibody or antigen-binding fragment thereof, of claim 1 , wherein the antigen-binding fragment is a Fab fragment, a Fab′ fragment, a Fd fragment, a Fd′ fragment, a Fv fragment, a dAb fragment, a F(ab′) 2 fragment, a single chain fragment, a diabody, or a linear antibody.
9. A pharmaceutical composition comprising the humanized antibody, or antigen-binding fragment thereof, of claim 1 , and a pharmaceutically acceptable excipient.
10. The pharmaceutical composition of claim 9 , further comprising an inhibitor of TGF-β signaling.
11. The composition of claim 10 , wherein the inhibitor of TGF-β signaling is selected from the group consisting of an antibody or antigen-binding fragment thereof that binds TGF-β, a receptor therefor, a double-stranded RNA or nucleic acid encoding a double-stranded RNA, an aptamer, and a small molecule.
12. The composition of claim 11 , wherein the small molecule is selected from the group consisting of 4-[4-(1,3-benzodioxol-5-yl)-5-pyridin-2-yl-1H-imidazol-2-yl]benzamide (SB431542), N-(oxan-4-yl)-4-[4-(5-pyridin-2-yl-1H-pyrazol-4-yl)pyridin-2-yl]benzamide (GW788388), 4-[3-(2-Pyridinyl)-1H-pyrazol-4-yl]-quinoline (LY364947), and 2-(3-(6-methylpyridin-2-yl)-1H-pyrazol-4-yl)-1,5-naphthyridine (“ALK5 Inhibitor II”).
13. The pharmaceutical composition of claim 9 , further comprising an immunomodulatory or chemotherapeutic agent.
14. The pharmaceutical composition of claim 13 , wherein the immunomodulatory agent comprises an immune checkpoint modulator.
15. The pharmaceutical composition of claim 13 , wherein the immunomodulatory agent comprises a tumor antigen vaccine.
16. The pharmaceutical composition of claim 15 , wherein the tumor antigen vaccine comprises a dendritic cell tumor antigen vaccine.
17. The pharmaceutical composition of claim 14 , wherein the immune checkpoint modulator modulates the effects of a polypeptide selected from the group consisting of PD-1, PD-L1, PDL2, CTLA4, LAG3, TIM3, TIGIT, and/or CD103.