Identification of shared characteristics in tumor-infiltrating T cells across 15 cancers

被引:9
作者
Jin, Xiyun [1 ]
Cai, Yideng [1 ]
Xue, Guangfu [1 ]
Que, Jinhao [1 ]
Cheng, Rui [1 ]
Yang, Yuexin [1 ]
Xiao, Lixing [1 ]
Lin, Xiaoyu [1 ]
Xu, Chang [1 ]
Wang, Pingping [2 ]
Xu, Zhaochun [1 ]
Nie, Huan [1 ]
Jiang, Qinghua [1 ,2 ,3 ]
机构
[1] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150000, Peoples R China
[2] Harbin Med Univ, Sch Interdisciplinary Med & Engn, Harbin 150076, Peoples R China
[3] Harbin Inst Technol, Key Lab Biol Big Data, Minist Educ, Harbin 150000, Peoples R China
来源
MOLECULAR THERAPY NUCLEIC ACIDS | 2023年 / 32卷
基金
中国国家自然科学基金;
关键词
REGULATORS; INFLAMMATION; NETWORKS; RECEPTOR; CD4;
D O I
10.1016/j.omtn.2023.03.007
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Tumor-infiltrating T cells are essential players in tumor immunotherapy. Great progress has been achieved in the investigation of T cell heterogeneity. However, little is well known about the shared characteristics of tumor-infiltrating T cells across cancers. In this study, we conduct a pan-cancer analysis of 349,799 T cells across 15 cancers. The results show that the same T cell types had similar expression patterns regulated by specific transcription factor (TF) regulons across cancers. Multiple T cell type transition paths were consistent in cancers. We found that TF regulons associated with CD8+ T cells transitioned to terminally differentiated effector memory (Temra) or exhausted (Tex) states were associated with patient clinical classification. We also observed universal activated cell-cell interaction pathways of tumor-infiltrating T cells in all cancers, some of which specifically mediated crosstalk in certain cell types. Moreover, consistent characteristics of TCRs in the aspect of variable and joining region genes were found across cancers. Overall, our study reveals common features of tumor-infiltrating T cells in different cancers and suggests future avenues for rational, targeted immunotherapies.
引用
收藏
页码:189 / 202
页数:14
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