Phenotypic and spatial heterogeneity of CD8+ tumour infiltrating lymphocytes

被引:1
|
作者
Sun, Yikan [1 ,2 ,3 ,4 ]
Yinwang, Eloy [1 ,2 ,3 ,4 ]
Wang, Shengdong [1 ,2 ,3 ,4 ]
Wang, Zenan [1 ,2 ,3 ,4 ]
Wang, Fangqian [1 ,2 ,3 ,4 ]
Xue, Yucheng [1 ,2 ,3 ,4 ]
Zhang, Wenkan [1 ,2 ,3 ,4 ]
Zhao, Shenzhi [1 ,2 ,3 ,4 ]
Mou, Haochen [1 ,2 ,3 ,4 ]
Chen, Shixin [1 ,2 ,3 ,4 ]
Jin, Lingxiao [1 ,2 ,3 ,4 ]
Li, Binghao [1 ,2 ,3 ,4 ]
Ye, Zhaoming [1 ,2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Orthoped Surg, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Orthoped Res Inst, Hangzhou, Zhejiang, Peoples R China
[3] Key Lab Motor Syst Dis Res & Precis Therapy Zhejia, Hangzhou, Zhejiang, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 2, Musculoskeletal Tumor Ctr, Sch Med,Dept Orthoped, Hangzhou 310009, Peoples R China
基金
中国国家自然科学基金;
关键词
CD8(+) T cells; Tumour-infiltrating lymphocytes; T cell nomenclature; T cell exclusion; Caner immunotypes; Cancer immunotherapy; CANCER-ASSOCIATED FIBROBLASTS; T-CELL DYSFUNCTION; MEMORY STEM-CELLS; RESIDENT MEMORY; DENDRITIC CELLS; B-CELLS; PREFERENTIAL LOCALIZATION; VIRAL-INFECTION; LOCAL IMMUNITY; PD-L1; BLOCKADE;
D O I
10.1186/s12943-024-02104-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CD8(+) T cells are the workhorses executing adaptive anti-tumour response, and targets of various cancer immunotherapies. Latest advances have unearthed the sheer heterogeneity of CD8(+) tumour infiltrating lymphocytes, and made it increasingly clear that the bulk of the endogenous and therapeutically induced tumour-suppressive momentum hinges on a particular selection of CD8(+) T cells with advantageous attributes, namely the memory and stem-like exhausted subsets. A scrutiny of the contemporary perception of CD8(+) T cells in cancer and the subgroups of interest along with the factors arbitrating their infiltration contextures, presented herein, may serve as the groundwork for future endeavours to probe further into the regulatory networks underlying their differentiation and migration, and optimise T cell-based immunotherapies accordingly.
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页数:21
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