Treatment of cancer with a semaphorin-4D antibody in combination with an epigenetic modulating agent
This disclosure provides a method for inhibiting, delaying, or reducing malignant cell growth in a subject with cancer, comprising administering to the subject a combination therapy comprising an effective amount of an isolated antibody or antigen-binding fragment thereof that specifically binds to semaphorin-4D (SEMA4D) and an effective amount of an epigenetic modulating agent, e.g., a histone deacetylase (HDAC) inhibitor (HDACi) a DNA methyltransferase (DNMT) inhibitor (DNMTi), or any combination thereof. The disclosure further provides a pharmaceutical composition comprising the combination therapy.
1. A method for inhibiting, delaying, or reducing malignant cell growth in a subject with colon cancer, comprising administering to the subject a combination therapy comprising an effective amount of an isolated antibody or antigen-binding fragment thereof that specifically binds to semaphorin-4D (SEMA4D) and an effective amount of an epigenetic modulating agent selected from Entinostat (Pyridin-3-ylmethyl N-[[4-[(2-aminophenyl) carbamoyl] phenyl] methyl]carbamate), azacytidine and a combination thereof, wherein the antibody or fragment thereof comprises a variable heavy chain (VH) comprising VH CDRs 1-3 comprising SEQ ID NOS: 2, 3, and 4, respectively, and a variable light chain (VL) comprising VL CDRs 1-3 comprising SEQ ID NOS: 6, 7, and 8, respectively.
2. The method of claim 1 , wherein the antibody or fragment thereof inhibits SEMA4D interaction with its receptor.
3. The method of claim 1 , wherein the antibody or fragment thereof inhibits SEMA4D-mediated Plexin-B1 signal transduction.
4. The method of claim 1 , wherein the VH and VL comprise, respectively, SEQ ID NO: 1 and SEQ ID NO: 5, or SEQ ID NO: 9 and SEQ ID NO: 10.
5. The method of claim 1 , wherein the epigenetic modulating agent is Entinostat (Pyridin-3-ylmethyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate).
6. The method of claim 1 , wherein the epigenetic modulating agent comprises azacytidine.
7. The method of claim 1 , wherein:
the isolated antibody or antigen-binding fragment thereof that specifically binds to semaphorin-4D (SEMA4D) comprises a VH comprising the amino acid sequence SEQ ID NO: 1 and a VL comprising the amino acid sequence SEQ ID NO: 5, and
the epigenetic modulating agent comprises the HDACi Entinostat or the DNMTi azacytidine.
8. A pharmaceutical composition for the treatment of colon cancer comprising an effective amount of an isolated antibody or antigen-binding fragment thereof that specifically binds to semaphorin-4D (SEMA4D) and an effective amount of an epigenetic modulating agent selected from Entinostat (Pyridin-3-ylmethyl N-[[4-[(2-aminophenyl) carbamoyl] phenyl] methyl]carbamate), azacytidine and a combination thereof, wherein the antibody or fragment thereof comprises a variable heavy chain (VH) comprising VH CDRs 1-3 comprising SEQ ID NOS: 2, 3, and 4, respectively, and a variable light chain (VL) comprising VL CDRs 1-3 comprising SEQ ID NOS: 6, 7, and 8, respectively.
9. The pharmaceutical composition of claim 8 , wherein the VH and VL comprise, respectively, SEQ ID NO: 1 and SEQ ID NO: 5, or SEQ ID NO: 9 and SEQ ID NO: 10.
10. The pharmaceutical composition of claim 8 , wherein the epigenetic modulating agent is Entinostat (Pyridin-3-ylmethyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate).
11. The pharmaceutical composition of claim 8 , wherein the epigenetic modulating agent is azacytidine.
12. A pharmaceutical composition for the treatment of colon cancer comprising:
an effective amount of an isolated antibody or antigen-binding fragment thereof that specifically binds to semaphorin-4D (SEMA4D), wherein the antibody or fragment thereof comprises the VH amino acid sequence SEQ ID NO: 1 and the VL amino acid sequence SEQ ID NO: 5, and
an effective amount of the HDACi Entinostat or an effective amount of the DNMTi azacytidine.