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 method of treating a cancer in a human subject in need thereof comprising administering a pharmaceutical composition comprising a humanized form of an antibody which binds latency-associated peptide (LAP), 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, to said human subject in an effective amount to decrease the number or activity of immunosuppressive T cells, thereby treating the cancer.
2. The method of claim 1 , wherein the humanized antibody or antigen-binding fragment thereof binds LAP on the surface of an immunosuppressive T cell associated with said cancer.
3. The method of claim 1 , wherein said immunosuppressive T cells infiltrate a tumor associated with said cancer.
4. The method of claim 3 , wherein said immunosuppressive T cells are regulatory T cells.
5. The method of claim 3 , wherein said tumor is a glioblastoma, a colorectal carcinoma, or a melanoma.
6. The method of claim 1 further comprising administering a chemotherapeutic or immunomodulatory agent to said subject.
7. The method of claim 6 , wherein the immunomodulatory agent comprises an immune checkpoint modulator.
8. The method of claim 7 , 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.
9. The method of claim 1 further comprising selecting said human subject as a candidate for treatment with the humanized antibody or antigen-binding fragment thereof:
identifying LAP+ T cells in said tumor of said human subject; and
selecting said human subject for treatment with the humanized antibody or antigen-binding fragment thereof on the basis of said identifying LAP+ T cells in said tumor.
10. The method of claim 1 , wherein binding of the humanized antibody or antigen-binding fragment thereof to a LAP-TGF-β complex inhibits release of TGF-β from said LAP-TGF-β complex.
11. The method of claim 1 , wherein the cancer is refractory to treatment with an immune checkpoint inhibitor.
12. The method of claim 1 , wherein the humanized antibody or antigen-binding fragment thereof 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.
13. The method 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.