Antibodies to programmed cell death protein 1
View Patent ↗Antibodies and antigen binding fragments thereof are provided that immunospecifically bind to PD-1, preferably human or mouse PD-1, and induce or promote an immune response that activates immune cell proliferation or activity. Contrary to the existing paradigm that PD-1 exclusively promotes a suppressive immune response, the disclosed antibodies and antigen binding fragments thereof, immunospecifically bind to PD-1 and cause an activating signal to be delivered to the immune cell that activates the immune cell rather than suppressing the immune cell. In one embodiment, the disclosed antibodies and antigen binding fragments thereof specifically bind to PD-1 expressed on immune cells. The binding of the disclosed antibodies and antigen binding fragments thereof to PD-1 on immune cells causes an activating signal to be transmitted into the immune cell, for example a signal that enhances or promotes cytokine production and/or activation of immune cell proliferation. Immune cells that express PD-1, include but are not limited to B and T cells as well as myeloid-derived cells. In one embodiment, the immune cell is a T cell, preferably a CD8+ T cell.
1. A method of inducing cellular activity in an immune cell that expresses programmed cell death receptor protein (PD-1), comprising contacting the immune cell with an antibody or antigen-binding fragment thereof that specifically binds to PD-1, wherein the antibody or antigen-binding fragment thereof comprises: (a) an HCDR1 domain having an amino acid sequence of SEQ ID NO: 18; (b) an HCDR2 domain having an amino acid sequence of SEQ ID NO: 19; (c) an HCDR3 domain having an amino acid sequence of SEQ ID NO: 20; (d) an LCDR1 domain having an amino acid sequence of SEQ ID NO: 24; (e) an LCDR2 domain having an amino acid sequence of SEQ ID NO: 13; and (f) an LCDR3 domain having an amino acid sequence of SEQ ID NO: 25.
2. The method of claim 1 , wherein the cellular activity comprises cell proliferation.
3. The method of claim 1 , wherein the cellular activity comprises cytokine activation.
4. The method of claim 1 , wherein the immune cell is a T cell.
5. The method of claim 4 , wherein the T cell is a CD8 T cell.
6. An isolated antibody or antigen-binding fragment thereof that binds specifically to PD-1, wherein the antibody comprises the three heavy chain CDRs (HCDR1, HCDR2 and HCDR3) contained within any one of the heavy chain variable region (HCVR) sequences selected from the group consisting of SEQ ID NOs:16 and 17; and the three light chain CDRs (LCDR1, LCDR2 and LCDR3) contained within any one of the light chain variable region (LCVR) sequences selected from the group consisting of SEQ ID NOs: 22 and 23.
7. The antibody or antigen-binding fragment thereof of claim 6 , comprising: (a) an HCDR1 domain having an amino acid sequence of SEQ ID NO: 18; (b) an HCDR2 domain having an amino acid sequence of SEQ ID NO: 19; (c) an HCDR3 domain having an amino acid sequence of SEQ ID NO: 20; (d) an LCDR1 domain having an amino acid sequence of SEQ ID NO: 24; (e) an LCDR2 domain having an amino acid sequence of SEQ ID NO: 13; and (f) an LCDR3 domain having an amino acid sequence of SEQ ID NO: 25.
8. A pharmaceutical composition comprising the antibody or antibody binding fragment thereof according to claim 6 .
9. The pharmaceutical composition of claim 8 , further comprising a second therapeutic agent.
10. The pharmaceutical composition of claim 9 , further comprising a pharmaceutically acceptable excipient.
11. The pharmaceutical composition of claim 10 , wherein the second therapeutic agent is a chemotherapeutic agent.
12. A method of inducing, promoting, or enhancing an immune response in a subject in need thereof, comprising administering to the subject an effective amount of the isolated antibody or antigen binding fragment of claim 6 , or the pharmaceutical composition of claim 8 , to induce, promote, or enhance an immune response in the subject.
13. A method for reducing tumor burden in a subject in need thereof, comprising administering to the subject an effective amount of the isolated antibody or antigen binding fragment of claim 6 , or the pharmaceutical composition of claim 8 to reduce tumor burden in the subject.
14. The method of claim 13 , wherein the tumor burden is from a bladder tumor, breast tumor, colorectal tumor, kidney tumor, liver tumor, lung tumor, ovary tumor, pancreas tumor, stomach tumor, cervical tumor, thyroid tumor, hematopoietic tumor of lymphoid lineage, hematopoietic tumor of myeloid lineage, tumor of the central and peripheral nervous system, or tumor of mesenchymal origin.
15. A method for treating an infection in a subject in need thereof, comprising, administering to the subject an effective amount of the antibody or antigen binding fragment of claim 6 , or the pharmaceutical composition of claim 8 , to treat the infection in the subject.