Chemoimmunotherapy

被引:83
作者
Emens, Leisha A. [1 ]
机构
[1] Johns Hopkins Univ, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr, Tumor Immunol Program, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
immunotherapy; chemotherapy; chemoimmunotherapy; cancer vaccines; adoptive cellular therapy; clinical trials; COLONY-STIMULATING FACTOR; REGULATORY T-CELLS; BONE-MARROW TRANSPLANTATION; ANTITUMOR IMMUNE-RESPONSE; CANCER-TESTIS ANTIGENS; B7-1; GENE-EXPRESSION; DENDRITIC CELLS; TUMOR-CELLS; IN-VIVO; PANCREATIC-CANCER;
D O I
10.1097/PPO.0b013e3181eb5066
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer chemotherapy drugs are historically regarded as detrimental to immunity because of their myelosuppressive effects. However, accumulating data suggest that the antitumor activity of conventional cancer chemotherapy results in part from its ability to harness the innate and adaptive immune systems by inducing immunologically active tumor cell death. Additional data broaden the immunologic effect of cancer chemotherapy drugs, demonstrating that some drugs have the ability to disrupt pathways of immune suppression and immune tolerance in a manner that depends on the drug dose, and the timing of its administration in relation to immunotherapy. Understanding the cellular and molecular basis of the interactions between chemotherapy drugs and the immune system will facilitate the strategic development of chemoimmunotherapy treatment regimens that both maximize tumor regression and the antitumor immune response for the long-term clinical benefit of cancer patients.
引用
收藏
页码:295 / 303
页数:9
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