Cytotoxic CD8+ Lymphocytes in the Tumor Microenvironment

被引:76
作者
Iwahori, Kota [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Clin Res Tumor Immunol, Osaka, Japan
[2] Osaka Univ, Grad Sch Med, Dept Resp Med & Clin Immunol, Osaka, Japan
来源
TUMOR MICROENVIRONMENT: HEMATOPOIETIC CELLS, PT A | 2020年 / 1224卷
关键词
Cytotoxic T cells; CD8(+) T cells; Tumor microenvironment; T-cell receptor; T-cell cytotoxicity; Tumor-specific antigen; Neoantigen; T-cell exhaustion; T-cell metabolism; Immune checkpoint inhibitor; PD-1; PD-L1; CTLA-4; Tumor mutation burden; Bispecific T-cell engager; SINGLE-CHAIN ANTIBODY; T-CELLS; ANTI-PD-1; ANTIBODY; RESIDENT MEMORY; E-CADHERIN; CANCER; SAFETY; CD28; CHEMOTHERAPY; NEOANTIGENS;
D O I
10.1007/978-3-030-35723-8_4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the tumor microenvironment, CD8(+) T cells play a major role in tumor immunity. CD8(+) T cells differentiate to cytotoxic T cells, traffic into the tumor microenvironment, and exhibit cytotoxicity against tumor cells. These processes have both positive and negative effects. Enhancements in the cytotoxic activity of tumor antigen-specific cytotoxic T cells in the tumor microenvironment are crucial for the development of cancer immunotherapy. To achieve this, several immunotherapies, including cancer vaccines, T cells engineered to express chimeric antigen receptors (CAR T cells), and bispecific T-cell engagers (BiTEs), have been developed. In contrast to cancer vaccines, CAR T cells, and BiTEs, immune checkpoint inhibitors enhance the activity of cytotoxic T cells by inhibiting the negative regulators of T cells. The total number, type, and activity of tumor antigen-specific cytotoxic T cells in the tumor microenvironment need to be clarified, particularly for the development of companion diagnostics to identify patients for whom these therapies are effective. Therefore, technologies including TCR repertoire, single-cell, and T-cell cytotoxicity analyses using BiTEs have been developed. Based on these and future innovations, the generation of effective cancer immunotherapies is anticipated.
引用
收藏
页码:53 / 62
页数:10
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