Fates of CD8+ T cells in Tumor Microenvironment

被引:348
作者
Maimela, Nomathamsanqa Resegofetse [1 ]
Liu, Shasha [1 ,2 ]
Zhang, Yi [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Biotherapy Ctr, Affiliated Hosp 1, 1 Jianshe East Rd, Zhengzhou 450052, Henan, Peoples R China
[2] Zhengzhou Univ, Canc Ctr, Affiliated Hosp 1, Zhengzhou 450052, Henan, Peoples R China
[3] Henan Key Lab Tumor Immunol & Biotherapy, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
CD8+ T cell fates; Tumor microenvironment; CD8+ T cell differentiation; CD8+ T cell trafficking; T cell exhaustion; SUPPRESSOR-CELLS; DENDRITIC CELLS; INFILTRATING LYMPHOCYTES; EFFECTOR FUNCTIONS; EPIGENETIC CONTROL; IMMUNE PRIVILEGE; DNA METHYLATION; CANCER; EXPRESSION; DIFFERENTIATION;
D O I
10.1016/j.csbj.2018.11.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies have reported a positive correlation between elevated CD8+ T cells in the tumor microenvironment (TME) and good prognosis in cancer. However, the mechanisms linking T cell tumor-infiltration and tumor rejection are yet to be fully understood. The cells and factors of the TME facilitate tumor development in various ways. CD8+ T cell function is influenced by a number of factors, including CD8+ T cell trafficicing and localization into tumor sites: as well as CD8+ T cell growth and differentiation. This review highlights recent literature as well as currently evolving concepts regarding the fates of CD8+ T cells in the TME from three different aspects CD8+ T cell trafficking, differentiation and function. A thorough understanding of factors contributing to the fates of CD8+ T cells will allow researchers to develop new strategies and improve on already existing strategies to facilitate CD8+ T cell mediated anti-tumor function, impede T cell dysfunction and modulate the TME into a less immunosuppressive TME. (C) 2018 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:1 / 13
页数:13
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