Signals for antigen-independent differentiation of memory CD8+ T cells

被引:4
|
作者
Kwesi-Maliepaard, Eliza Mari [1 ]
Jacobs, Heinz [2 ]
van Leeuwen, Fred [1 ,3 ]
机构
[1] Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Div Tumor Biol & Immunol, NL-1066 CX Amsterdam, Netherlands
[3] Univ Amsterdam, Amsterdam UMC, Dept Med Biol, NL-1105 AZ Amsterdam, Netherlands
关键词
CD8(+) T cell; Antigen-inexperienced memory; Virtual memory; Innate memory; HISTONE DEACETYLASE 7; H3K79; METHYLATION; CORD BLOOD; INNATE; EFFECTOR; NAIVE; IL-4; TRANSCRIPTION; PHENOTYPE; MICE;
D O I
10.1007/s00018-021-03912-9
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
Conventional CD8(+) memory T cells develop upon stimulation with foreign antigen and provide increased protection upon re-challenge. Over the past two decades, new subsets of CD8(+) T cells have been identified that acquire memory features independently of antigen exposure. These antigen-inexperienced memory T cells (T-AIM) are described under several names including innate memory, virtual memory, and memory phenotype. T-AIM cells exhibit characteristics of conventional or true memory cells, including antigen-specific responses. In addition, they show responsiveness to innate stimuli and have been suggested to provide additional levels of protection toward infections and cancer. Here, we discuss the current understanding of T-AIM cells, focusing on extrinsic and intrinsic molecular conditions that favor their development, their molecular definitions and immunological properties, as well as their transcriptional and epigenetic regulation.
引用
收藏
页码:6395 / 6408
页数:14
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