Tissue-Resident Memory T Cells in Cancer Immunosurveillance

被引:140
|
作者
Park, Simone L. [1 ]
Gebhardt, Thomas [1 ]
Mackay, Laura K. [1 ]
机构
[1] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Vic, Australia
关键词
TUMOR-INFILTRATING LYMPHOCYTES; TGF-BETA; NEOANTIGEN LANDSCAPE; NONLYMPHOID TISSUES; ADAPTIVE IMMUNITY; RM CELLS; CD103; SKIN; MELANOMA; DIFFERENTIATION;
D O I
10.1016/j.it.2019.06.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Following their activation and expansion in response to foreign threats, many T cells are retained in peripheral tissues without recirculating in the blood. These tissue-resident CD8(+) memory T (TRM) cells patrol barrier surfaces and nonlymphoid organs, where their critical role in protecting against viral and bacterial infections is well established. Recent evidence suggests that TRM cells also play a vital part in preventing the development and spread of solid tumors. Here, we discuss the emerging role of TRM cells in anticancer immunity. We highlight defining features of tumor-localizing TRM cells, examine the mechanisms through which they have recently been shown to suppress cancer growth, and explore their potential as future targets of cancer immunotherapy.
引用
收藏
页码:735 / 747
页数:13
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