Cellular Constituents of Immune Escape within the Tumor Microenvironment

被引:401
作者
Kerkar, Sid P. [1 ,2 ]
Restifo, Nicholas P. [1 ]
机构
[1] NCI, Surg Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Hematol Branch, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
COLONY-STIMULATING FACTOR; T-REGULATORY CELLS; SUPPRESSOR-CELLS; DENDRITIC CELLS; MYELOID CELLS; CANCER-IMMUNOTHERAPY; INFLAMMATION; MACROPHAGES; LYMPHOCYTES; INHIBITION;
D O I
10.1158/0008-5472.CAN-11-4094
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Established tumors are complex masses that contain not only neoplastic cells but also nontransformed cellular elements such as stromal cells, the neovasculature, and the full gamut of immune cells. However, evidence suggests that, unlike cells found in lymphoid organs that productively respond to acute infections, immune cells in tumors are dysregulated and functionally impaired. Tumor masses can contain regulatory lymphocytes, myeloid-derived suppressor cells, alternatively activated macrophages, and dendritic cells. Ablation or reprogramming of this aberrant microenvironment might dramatically augment cancer therapies, and this strategy is currently being deployed in a variety of clinical trials. A better understanding of the cellular constituents of tumors and the mechanisms involved in immune evasion may help guide the next generation of innovative cancer immunotherapies. Cancer Res; 72(13); 3125-30. (C) 2012 AACR.
引用
收藏
页码:3125 / 3130
页数:6
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