Chemokine receptor antagonists as therapeutic agents
View Patent ↗The present invention provides methods and compositions to reduce immune tolerance at specific sites. In one aspect, the present invention comprises methods and compositions to reduce tumorigenicity. In an embodiment, the present invention reduces recruitment of tolerance-inducing antigen presenting cells (APCs) or their precursors to a tumor and/or tumor draining lymph node by decreasing binding of at least one tumor-associated ligand to a chemokine receptor present on the tolerance-inducing APCs or APC precursors. In an embodiment, the chemokine receptor is CCR6 and the tumor-associated ligand is mip-3α. In another aspect, the present invention comprises methods and compositions to reduce immune tolerance to a virus. In an embodiment, the virus is HIV. The present invention further provides for the development of CCR6 antibodies and antagonists as therapeutic agents to prevent or reduce immune tolerance.
1. A method to reduce recruitment of IDO+ dendritic cells that inhibit T-cell proliferation to at least one of a tumor or a tumor-draining lymph node in a subject comprising administering a composition comprising an antibody to CCR6 to the subject, wherein the IDO+ dendritic cells express CCR6 and elevated levels of indoleamine 2,3-dioxygenase (IDO), and tumor cells of the at least one of a tumor or a tumor draining lymph node express MIP-3a.
2. The method of claim 1 , wherein the subject is human.
3. The method of claim 1 , wherein the CCR6 antibody blocks the interaction between the CCR6 expressed by the IDO+ dendritic cells and the MIP-3α expressed by tumor cells of the at least one of a tumor or a tumor draining lymph node.
4. The method of claim 1 , further comprising the step of determining that IDO+ dendritic cells are recruited to the at least one of a tumor or a tumor-draining lymph node.
5. The method of claim 1 , wherein the MIP-3α mediates recruitment of the IDO+ dendritic cells to the at least one of a tumor or a tumor draining lymph node.