Methods and compositions for treating solid tumors and enhancing tumor vaccines
The present invention provides methods of treating and enhancing efficacy of immunotherapy for a solid tumor in a subject, comprising the step of contacting the subject with a compound or composition that modulates the expression or activity of ETRB, ET-1, ICAM-1, or another protein found herein to play a role in homing of T cells to a solid tumor. The present invention also provides methods of prognosticating a solid tumor in a subject, comprising the step of measuring an expression level of a protein found herein to play a role in homing of T cells to a solid tumor, or a nucleotide molecule encoding same.
1. A method of treating a solid tumor expressing Endothelin B receptor (ETRB) in a subject, comprising: administering to said subject a therapeutically effective amount of a tumor cell-based vaccine that activates a cytotoxic, tumor-antigen specific T-cell response; and administering to said vaccinated subject a therapeutically effective amount of an Endothelin B receptor (ETRB) inhibitor to enhance the efficacy of said vaccine, and wherein the ETRB inhibitor is selected from the group consisting of BQ788, Bosentan, tezosentan, and an antibody.
2. The method of claim 1 , wherein said inhibitor BQ788.
3. The method of claim 1 , wherein said tumor cell-based vaccine comprises apoptotic tumor cells.
4. The method of claim 1 , wherein said subject is a human subject.
5. The method of claim 1 , wherein expression or activity of an intercellular adhesion molecule 1 (ICAM-1 protein) is increased.
6. A method of enhancing the efficacy of a tumor cell-based vaccine for a solid tumor expressing Endothelin B receptor (ETRB) in a subject, comprising the steps of: administering a therapeutically effective amount of the tumor cell-based to the subject, and contacting said subject with an Endothelin B receptor (ETRB) inhibitor in an effective amount to enhance the efficacy of the vaccine for the solid tumor in said subject, and wherein the ETRB inhibitor is selected from the group consisting of BQ788, Bosentan, tezosentan, and an antibody, and wherein said vaccine activates a cytotoxic, tumor-antigen specific T-cell response.
7. The method of claim 6 , wherein said inhibitor is BQ788.
8. The method of claim 6 , wherein said tumor cell-based vaccine comprises apoptotic tumor cells.
9. The method of claim 6 , wherein expression or activity of an intercellular adhesion molecule 1 (ICAM-1 protein) is increased.
10. A method of delaying growth of a solid tumor expressing Endothelin B receptor (ETRB) in a subject, comprising: administering to said subject a therapeutically effective amount of a tumor cell-based vaccine that activates a cytotoxic, tumor-antigen specific T-cell response; and administering to said vaccinated subject a therapeutically effective amount of an Endothelin B receptor (ETRB) inhibitor to enhance the efficacy of said vaccine, and wherein the ETRB inhibitor is selected from the group consisting of BQ788, Bosentan, tezosentan, and an antibody.
11. The method of claim 10 , wherein said tumor cell-based vaccine comprises apoptotic tumor cells.
12. A method for identifying and treating a subject who is likely to benefit from a combination therapy comprising administering a tumor cell-based vaccine that activates a cytotoxic, tumor-antigen specific T-cell response, and an Endothelin B receptor (ETRB) blockade to treat a solid tumor, said method comprising the steps of
a. measuring an expression level of an Endothelin B receptor (ETRB) or a nucleotide molecule encoding an Endothelin B receptor (ETRB) in said solid tumor;
b. comparing said expression level to a reference standard comprising a normal vascular sample, and
c. administering to said subject a therapeutically effective amount of said tumor cell-based vaccine; and administering to said subject a therapeutically effective amount of an Endothelin B receptor (ETRB) inhibitor to enhance the efficacy of said vaccine, and wherein the ETRB inhibitor is selected from the group consisting of BQ788, Bosentan, tezosentan, and an antibody, if said expression level is higher than said reference standard.