4-1BB binding molecules
The present disclosure provides isolated binding molecules that bind to human 4-1BB, nucleic acid molecules encoding an amino acid sequence of the binding molecules, vectors comprising the nucleic acid molecules, host cells containing the vectors, methods of making the binding molecules, pharmaceutical compositions containing the binding molecules, and methods of using the binding molecules or compositions.
1. An isolated antibody, or antigen-binding portion thereof, comprising:
a H-CDR1 amino acid sequence as set forth in SEQ ID NO:1 or 15, a H-CDR2 amino acid sequence as set forth in SEQ ID NO:2 or 16, a H-CDR3 amino acid sequence as set forth in SEQ ID NO:3 or 17, a L-CDR1 amino acid sequence as set forth in SEQ ID NO:6 or 20, a L-CDR2 amino acid sequence as set forth in SEQ ID NO:7 or 21, and a L-CDR3 amino acid sequence as set forth in SEQ ID NO:8 or 22.
2. The isolated antibody, or antigen-binding portion thereof, according to claim 1 comprising:
a H-CDR1 amino acid sequence as set forth in SEQ ID NO:1, a H-CDR2 amino acid sequence as set forth in SEQ ID NO:2, a H-CDR3 amino acid sequence as set forth in SEQ ID NO:3, a L-CDR1 amino acid sequence as set forth in SEQ ID NO:6, a L-CDR2 amino acid sequence as set forth in SEQ ID NO:7 and a L-CDR3 amino acid sequence as set forth in SEQ ID NO:8; or
a H-CDR1 amino acid sequence as set forth in SEQ ID NO:15, a H-CDR2 amino acid sequence as set forth in SEQ ID NO:16, a H-CDR3 amino acid sequence as set forth in SEQ ID NO:17, a L-CDR1 amino acid sequence as set forth in SEQ ID NO:20, a L-CDR2 amino acid sequence as set forth in SEQ ID NO:21 and a L-CDR3 amino acid sequence as set forth in SEQ ID NO:22.
3. The isolated antibody, or antigen-binding portion thereof, according to claim 1 comprising a VH region amino acid sequence as set forth in SEQ ID NO:4 or 18.
4. The isolated antibody, or antigen-binding portion thereof, according to claim 1 comprising a VL region amino acid sequence as set forth in SEQ ID NO:9 or 23.
5. The isolated antibody, or antigen-binding portion thereof, according to claim 1 , comprising:
a V H region amino acid sequence as set forth in SEQ ID NO:4 and a V L region amino acid sequence as set forth in SEQ ID NO:9, or
a V H region amino acid sequence as set forth in SEQ ID NO:18 and a V L region amino acid sequence as set forth in SEQ ID NO:23.
6. The isolated antibody, or antigen-binding portion thereof, according to claim 1 , comprising:
a heavy chain amino acid sequence as set forth in SEQ ID NO:5 and a light chain amino acid sequence set forth in SEQ ID NO:10, or
a heavy chain amino acid sequence as set forth in SEQ ID NO:19 and a light chain amino acid sequence set forth in SEQ ID NO:24.
7. A pharmaceutical composition comprising the antibody, or antigen-binding portion thereof, according to claim 1 and a pharmaceutically acceptable carrier.
8. A method for reducing tumor growth in a subject in need thereof, comprising administering to the subject an effective amount of an antibody or antigen-binding portion thereof, according to claim 1 , and a pharmaceutically acceptable carrier.
9. A method of treating cancer in a subject in need thereof, comprising administering an effective amount of an antibody or antigen-binding portion thereof, according to claim 1 , and a pharmaceutically acceptable carrier.
10. The method according to claim 9 , wherein the cancer is selected from the group consisting of colorectal cancer, non-Hodgkin's lymphoma, prostate cancer, or melanoma.
11. A method of treating cancer in a subject in need thereof, comprising administering an effective amount of an antibody or antigen-binding portion thereof, according to claim 1 , in combination with an immunotherapeutic agent.