Agonist antibodies that bind human CD137 and uses thereof
The present disclosure relates to compounds (e.g., antibodies, or antigen-binding fragments thereof) that bind to an epitope of CD137 and agonize CD137, and to use of the compounds in methods for treating, or ameliorating one or more symptoms of, cancer.
1. A method of treating cancer in a subject, comprising administering to the subject an isolated monoclonal antibody, or antigen binding portion thereof, that specifically binds human CD137, wherein the antibody or antigen binding portion thereof comprises heavy and light chain variable regions comprising the amino acid sequences of SEQ ID NOs: 4 and 6, respectively, thereby treating cancer in the subject.
2. The method of claim 1 , wherein the antibody or antigen binding portion thereof comprises an IgG1 heavy chain constant region.
3. The method of claim 2 , wherein the IgG1 heavy chain constant region is a wild-type human IgG1 heavy chain constant region.
4. The method of claim 2 , wherein the IgG1 heavy chain constant region comprises an amino acid substitution relative to a wild-type human IgG1 heavy chain constant region.
5. The method of claim 1 , wherein the antibody or antigen binding portion thereof comprises an IgG4 heavy chain constant region.
6. The method of claim 5 , wherein the IgG4 heavy chain constant region is a wild-type human IgG4 heavy chain constant region.
7. The method of claim 5 , wherein the IgG4 heavy chain constant region comprises an amino acid substitution relative to a wild-type human IgG4 heavy chain constant region.
8. The method of claim 7 , wherein the amino acid substitution is at position Ser228 according to EU numbering.
9. The method of claim 8 , wherein the amino acid substitution is S228P.
10. A method of treating cancer in a subject, comprising administering to the subject an isolated monoclonal antibody that specifically binds human CD137, wherein the antibody comprises heavy and light chains comprising the amino acid sequences of SEQ ID NOs: 129 and 133, respectively, thereby treating cancer in the subject by inducing or enhancing an anti tumor immune response.
11. A method of treating cancer in a subject, comprising administering to the subject a pharmaceutical composition comprising an isolated monoclonal antibody, or antigen binding portion thereof, that specifically binds human CD137, and a pharmaceutically acceptable carrier, wherein the antibody or antigen binding portion thereof comprises heavy and light chain variable regions comprising the amino acid sequences of SEQ ID NOs: 4 and 6, respectively, thereby treating cancer in the subject.
12. The method of claim 11 , wherein the antibody or antigen binding portion thereof comprises an IgG1 heavy chain constant region.
13. The method of claim 12 , wherein the IgG1 heavy chain constant region is a wild-type human IgG1 heavy chain constant region.
14. The method of claim 12 , wherein the IgG1 heavy chain constant region comprises an amino acid substitution relative to a wild-type human IgG1 heavy chain constant region.
15. The method of claim 11 , wherein the antibody or antigen binding portion thereof comprises an IgG4 heavy chain constant region.
16. The method of claim 15 , wherein the IgG4 heavy chain constant region is a wild-type human IgG4 heavy chain constant region.
17. The method of claim 15 , wherein the IgG4 heavy chain constant region comprises an amino acid substitution relative to a wild-type human IgG4 heavy chain constant region.
18. The method of claim 17 , wherein the amino acid substitution is at position Ser228 according to EU numbering.
19. The method of claim 18 , wherein the amino acid substitution is S228P.
20. A method of treating cancer in a subject, comprising administering to the subject a pharmaceutical composition comprising an isolated monoclonal antibody that specifically binds human CD137, and a pharmaceutically acceptable carrier, wherein the antibody comprises heavy and light chains comprising the amino acid sequences of SEQ ID NOs: 129 and 133, respectively, thereby treating cancer in the subject.