Antitumor T-cell responses contribute to the effects of dasatinib on c-KIT mutant murine mastocytoma and are potentiated by anti-OX40

作者：Yang, Yan; Liu, Chengwen; Peng, Weiyi; Lizee, Gregory; Overwijk, Willem W.; Liu, Yang; Woodman, Scott E.; Hwu, Patrick^*

来源：Blood, 2012, 120(23): 4533-4543.

DOI：10.1182/blood-2012-02-407163

• TYROSINE KINASE INHIBITOR
• IN-VITRO
• TUMOR
• ANTIGEN
• OX40
• MELANOMA
• PROLIFERATION
• CHEMOTHERAPY
• BMS-354825
• INTERLEUKIN-2

Targeted and immune-based therapies are thought to eradicate cancer cells by different mechanisms, and these approaches could possibly complement each other when used in combination. In this study, we report that the in vivo antitumor effects of the c-KIT inhibitor, dasatinib, on the c-KIT mutant P815 mastocytoma tumor were substantially dependent on T cell-mediated immunity. We found that dasatinib treatment significantly decreased levels of Tregs while specifically enhancing tumor antigen-specific T-cell responses. We sought to further enhance this therapy with the addition of anti-OX40 antibody, which is known to provide a potent costimulatory signal to T cells. The combination of dasatinib and anti-OX40 antibody resulted in substantially better therapeutic efficacy compared with either drug alone, and this was associated with enhanced accumulation of tumor antigen-specific T cells in the tumor microenvironment. Furthermore, the combination regimen inhibited the function of Tregs and also resulted in significantly up-regulated expression of the IFN-gamma-induced chemokines CXCL9, 10, and 11 in the tumor microenvironment, which provides a feasible mechanism for the enhanced intratumoral CTL infiltration. These studies delineate a strategy by which targeted therapy and immunotherapy may be combined to achieve superior antitumor responses in cancer patients. (Blood. 2012;120(23):4533-4543)

• 出版日期2012-11-29