Targeting Innate Immunity to Enhance the Efficacy of Radiation Therapy

被引:44
作者
Dar, Tahir B. [1 ]
Henson, Regina M. [1 ]
Shiao, Stephen L. [1 ,2 ]
机构
[1] Cedars Sinai Med Ctr, Dept Radiat Oncol, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Biomed Sci, Los Angeles, CA 90048 USA
关键词
radiation therapy; innate and adaptive immune response; immunotherapy; macrophages; dendritic cells; NK cells; TUMOR-ASSOCIATED MACROPHAGES; COLONY-STIMULATING FACTOR; TLR7 AGONIST IMIQUIMOD; RECEPTOR; 7; AGONIST; T-CELL RESPONSES; DENDRITIC CELLS; IONIZING-RADIATION; IFN-GAMMA; ANTICANCER CHEMOTHERAPY; ANTITUMOR IMMUNITY;
D O I
10.3389/fimmu.2018.03077
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Radiation continues to play a major role in the treatment of almost every cancer type. Traditional radiation studies focused on its ability to damage DNA, but recent evidence has demonstrated that a key mechanism driving the efficacy of radiation in vivo is the immune response triggered in irradiated tissue. Innate immune cells including macrophages, dendritic cells, and natural killer cells are key mediators of the radiation-induced immune response. They regulate the sensing of radiation-mediated damage and subsequent radiation-induced inflammation. Given the importance of innate immune cells as determinants of the post-radiation anti-tumor immune response, much research has been devoted to identify ways to both enhance the innate immune response and prevent their ability to suppress ongoing immune responses. In this review, we will discuss how the innate immune system shapes anti-tumor immunity following radiation and highlight key strategies directed at the innate immune response to enhance the efficacy of radiation.
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页数:11
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