Reprogramming the tumor microenvironment: tumor-induced immunosuppressive factors paralyze T cells

被引:205
|
作者
Wu, Annie A. [1 ]
Drake, Virginia [2 ]
Huang, Huai-Shiuan [3 ]
Chiu, ShihChi [3 ]
Zheng, Lei [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[2] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[3] Natl Taiwan Univ, Coll Med, Taipei 10764, Taiwan
来源
ONCOIMMUNOLOGY | 2015年 / 4卷 / 07期
关键词
immunosuppression; immunotherapy; immunosuppressive factors; T cells; tumor microenvironment; GROWTH-FACTOR-BETA; BCL-X-L; INDOLEAMINE 2,3-DIOXYGENASE EXPRESSION; MYELOID SUPPRESSOR-CELLS; SMALL-MOLECULE INHIBITOR; PROSTATE-CANCER CELLS; HUMAN-MELANOMA CELLS; DOWN-REGULATION; IMMUNE-RESPONSES; GENE-EXPRESSION;
D O I
10.1080/2162402X.2015.1016700
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has become evident that tumor-induced immunosuppressive factors in the tumor microenvironment play a major role in suppressing normal functions of effector T cells. These factors serve as hurdles that limit the therapeutic potential of cancer immunotherapies. This review focuses on illustrating the molecular mechanisms of immunosuppression in the tumor microenvironment, including evasion of T-cell recognition, interference with T-cell trafficking, metabolism, and functions, induction of resistance to T-cell killing, and apoptosis of T cells. A better understanding of these mechanisms may help in the development of strategies to enhance the effectiveness of cancer immunotherapies.
引用
收藏
页码:1 / 14
页数:14
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