期刊
TUMOR BIOLOGY
卷 39, 期 3, 页码 -出版社
SAGE PUBLICATIONS LTD
DOI: 10.1177/1010428317695021
关键词
Adenosine; cancer; CD73; dendritic cell; immunotherapy
类别
资金
- Tehran University of Medical Sciences [92-03-87-23034]
Dendritic cells are important in initiating immune responses; therefore, a range of dendritic cell-based approaches have been established to induce immune response against cancer cells. However, the presence of immunosuppressive mediators such as adenosine in the tumor microenvironment reduces the efficacy of dendritic cell-based cancer immunotherapy. In this study, we investigated whether blockade of the A2A adenosine receptor with a selective antagonist and a CD73 inhibitor may increase the efficacy of a dendritic cell-based cancer vaccine. According to the findings, this therapeutic combination reduced tumor growth, prolonged survival of tumor-bearing mice, and enhanced specific antitumor immune responses. Thus, we suggest that targeting cancer-derived adenosine improves the outcomes of dendritic cell-based cancer immunotherapy.
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