Methods and compositions for the treatment of persistent infections and cancer by inhibiting the programmed cell death 1 (PD-1) pathway
The present invention provides methods and compositions for the treatment, prevention, or reduction of persistent infections, such as chronic infections, latent infections, and slow infections and cancer. The methods and compositions of the invention are also useful for the alleviation of one or more symptoms associated with such infections and cancer.
1. A method of increasing cytotoxic activity of anergic T cells in a subject having a lymphoproliferative cancer, comprising
administering to the subject having the lymphoproliferative cancer an effective amount of an agent that reduces the activity of a Programmed Cell Death (PD)-1 polypeptide, wherein the agent is an anti-PD-1 antibody,
thereby increasing the cytotoxic activity of anergic T cells in the subject with the lymphoproliferative cancer, wherein the lymphoproliferative cancer is a Hodgkin's lymphoma.
2. The method of claim 1 , wherein increasing the cytotoxic activity of anergic T cells comprises increasing cytokine production or T cell proliferation.
3. The method of claim 2 , wherein the cytokine is interferon γ, tumor necrosis factor α or interleukin -2.
4. The method of claim 1 , further comprising measuring cytotoxic T cell activity in a biological sample from the subject.
5. The method of claim 4 , wherein measuring cytotoxic T cell activity comprises measuring the cytotoxic activity of anergic CD8+ T cells in the biological sample from the subject.
6. The method of claim 4 , wherein measuring cytotoxic T cell activity comprises measuring the production of a cytokine by T cells in the biological sample from the subject.
7. The method of claim 6 , wherein the cytokine is interferon γ, tumor necrosis factor α or interleukin -2.
8. The method of claim 1 , wherein the Hodgkin's lymphoma is a nodular lymphocyte predominant Hodgkin's lymphoma.
9. The method of claim 1 , wherein the method further comprises administering to the subject an effective amount of a second compound that induces an immune response.
10. The compound of claim 9 , wherein the second compound is an anti-inflammatory compound, an antineoplastic compound or an analgesic.
11. The method of claim 9 , wherein the second compound is an anti-CTLA-4 antibody, an anti-BTLA antibody, or an anti-B7-H4 antibody.
12. The method of claim 11 , wherein the second compound reduces cancer cell volume.
13. The method of claim 1 , wherein the antibody is a monoclonal antibody, a humanized antibody, a deimmunized antibody, or an immunoglobulin (Ig) fusion protein.
14. The method of claim 1 , wherein the subject is human.
15. The method of claim 1 , wherein the method decreases a symptom of the lymphoproliferative cancer in the subject.
16. The method of claim 1 , wherein the method decreases the size of the tumor or the prevalence of cancer cells.
17. A method of increasing cytotoxic activity of anergic T cells in a subject having a lymphoproliferative cancer, comprising
administering to the subject having the lymphoproliferative cancer an effective amount of (a) an agent that reduces the activity of a Programmed Cell Death (PD)-1 polypeptide, wherein the agent is an anti-PD-1 antibody or an anti-Programmed Cell Death Ligand (PD-L1) antibody, and (b) an anti-CTLA-4 antibody,
thereby increasing the cytotoxic activity of anergic T cells in the subject with the lymphoproliferative cancer, wherein the lymphoproliferative cancer is a Hodgkin's lymphoma or angioimmunoblastic T cell lymphoma.
18. The method of claim 17 , wherein the Hodgkin's lymphoma is a nodular lymphocyte predominant Hodgkin's lymphoma.
19. The method of claim 17 , wherein the subject is human.
20. The method of claim 17 , wherein the anti-PD-L1 antibody is a monoclonal antibody, a humanized antibody, a deimmunized antibody, or an immunoglobulin (Ig) fusion protein.
21. The method of claim 17 , wherein the anti-PD-1 antibody is a monoclonal antibody, a humanized antibody, a deimmunized antibody, or an immunoglobulin (Ig) fusion protein.