IL-23R antagonists to reprogram intratumoral T regulatory cells into effector cells
Provided by the disclosure are compositions and methods for modulating differentiation of regulatory T cells. In some embodiments, methods include selectively decreasing IL-23R activity and/or IL-23R expression without significantly decreasing IL-12RP activity and/or IL-12RP expression.
1. A method for treating cancer in a human subject, the method comprising:
administering to a human subject in need thereof an agent that decreases IL-23R activity and does not decrease IL-12Rβ activity, in an amount effective to treat the cancer;
wherein the agent is a human or humanized antibody derived from mouse monoclonal antibody 12B2B64;
wherein the antibody binds IL-23R and does not bind IL-12Rβ; and
wherein the antibody binds to an epitope of IL-23R on regulatory T (Treg) cells, comprising the amino acid sequence of SEQ ID NO: 3 or SEQ ID NO: 4.
2. The method of claim 1 , wherein the agent decreases IL-23R activity and does not decrease IL-12Rβ activity in the Treg cells.
3. The method of claim 1 , wherein the antibody has 100-fold, 1,000-fold, or 10,000-fold greater binding affinity for IL-23R than for IL-12Rβ.
4. The method of claim 1 , wherein the antibody binds the extracellular domain of IL-23R.
5. The method of claim 1 , wherein binding of the antibody to the epitope of IL-23R converts the Treg cells to effector T (Teff) cells.
6. The method of claim 1 , wherein the antibody is free of antibody dependent cellular cytotoxicity (ADCC) activity.
7. The method of claim 1 , wherein the human or humanized antibody has an IgG4 heavy chain immunoglobulin constant domain.
8. The method of claim 1 , wherein the antibody is administered to the subject in an amount of about 0.1 to 300 mg/kg of the body weight of the subject divided into one or more doses.
9. The method of claim 1 , further comprising administering to the human subject an immunomodulatory agent.
10. The method of claim 9 , wherein the immunomodulatory agent is an immune checkpoint inhibitor.
11. The method of claim 10 , wherein the immune checkpoint inhibitor is an antagonist of a molecule selected from the group consisting of PD-1, TIM-3, TIGIT, VISTA, A2AR, B7-H3, B7-H4, BTLA, CTLA-4, IDO, KIR and LAG3.
12. The method of claim 1 , further comprising administering to the human subject an agent that inhibits cancer cell growth.
13. The method of claim 1 , further comprising measuring activation of STAT3, STAT5, and/or IFN-□ in the human subject following administration of the agent.
14. The method of claim 13 , wherein STAT3 expression is increased, STAT5 expression is decreased, and/or IFN-γ expression is increased, relative to a control subject.
15. The method of claim 1 , wherein the cancer is a melanoma or colorectal cancer.