Revealing Clonal Responses of Tumor-Reactive T-Cells Through T Cell Receptor Repertoire Analysis

被引:16
作者
Aoki, Hiroyasu [1 ,2 ]
Shichino, Shigeyuki [1 ]
Matsushima, Kouji [1 ]
Ueha, Satoshi [1 ]
机构
[1] Tokyo Univ Sci, Res Inst Biomed Sci, Div Mol Regulat Inflammatory & Immune Dis, Chiba, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Hyg, Tokyo, Japan
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
日本学术振兴会;
关键词
CD8(+) T cell; T-cell receptor repertoire; single-cell TCR-seq; immune check inhibitors; cancer-immunity cycle; inter-organ clone tracking; PD-1; BLOCKADE;
D O I
10.3389/fimmu.2022.807696
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8(+) T cells are the key effector cells that contribute to the antitumor immune response. They comprise various T-cell clones with diverse antigen-specific T-cell receptors (TCRs). Thus, elucidating the overall antitumor responses of diverse T-cell clones is an emerging challenge in tumor immunology. With the recent advancement in next-generation DNA sequencers, comprehensive analysis of the collection of TCR genes (TCR repertoire analysis) is feasible and has been used to investigate the clonal responses of antitumor T cells. However, the immunopathological significance of TCR repertoire indices is still undefined. In this review, we introduce two approaches that facilitate an immunological interpretation of the TCR repertoire data: inter-organ clone tracking analysis and single-cell TCR sequencing. These approaches for TCR repertoire analysis will provide a more accurate understanding of the response of tumor-specific T cells in the tumor microenvironment.
引用
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页数:10
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