Role of CD8+ T lymphocyte cells: Interplay with stromal cells in tumor microenvironment

被引:59
|
作者
Xie, Qin [1 ,2 ]
Ding, Jian [2 ,4 ,5 ]
Chen, Yi [2 ,3 ]
机构
[1] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310012, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, Div Antitumor Pharmacol, Shanghai 201203, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[5] Shanghai HaiHe Pharmaceut Co Ltd, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
CD8(+) T lymphocyte; Stromal cell; Tumor microenvironment; Immunosuppression; Immunotherapy; Antitumor; CANCER-ASSOCIATED FIBROBLASTS; INHIBITORY RECEPTORS; IMMUNE ESCAPE; B7; FAMILY; TGF-BETA; ABERRANT EXPRESSION; PD-1; EXPRESSION; LUNG-CANCER; CTLA-4; ACTIVATION;
D O I
10.1016/j.apsb.2021.03.027
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CD8(+) T lymphocytes are pivotal cells in the host response to antitumor immunity. Tumor-driven microenvironments provide the conditions necessary for regulating infiltrating CD8(+) T cells in favor of tumor survival, including weakening CD8(+) T cell activation, driving tumor cells to impair immune attack, and recruiting other cells to reprogram the immune milieu. Also in tumor microenvironment, stromal cells exert immunosuppressive skills to avoid CD8(+) T cell cytotoxicity. In this review, we explore the universal function and fate decision of infiltrated CD8(+) T cells and highlight their antitumor response within various stromal architectures in the process of confronting neoantigen-specific tumor cells. Thus, this review provides a foundation for the development of antitumor therapy based on CD8(+) T lymphocyte manipulation. (C) 2021 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:1365 / 1378
页数:14
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