Defining Memory CD8 T Cell

被引:305
作者
Martin, Matthew D. [1 ]
Badovinac, Vladimir P. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Microbiol & Immunol, Iowa City, IA 52242 USA
[3] Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USA
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
基金
美国国家卫生研究院;
关键词
CD8 T cell; memory; subsets; heterogeneity; protection; outbred mice; age of memory; history of Ag enounters; ANTIGEN EXPOSURE HISTORY; IL-7; RECEPTOR-ALPHA; RESIDENT MEMORY; IN-VIVO; COLLABORATIVE CROSS; CUTTING EDGE; TRANSCRIPTION FACTORS; LINEAGE RELATIONSHIP; NONLYMPHOID TISSUES; PROTECTIVE IMMUNITY;
D O I
10.3389/fimmu.2018.02692
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 comprising the memory pool display considerable heterogeneity, with individual cells differing in phenotype and function. This review will focus on our current understanding of heterogeneity within the antigen-specific memory CD8 T cell compartment and classifications of memory CD8 T cell subsets with defined and discrete functionalities. Recent data suggest that phenotype and/or function of numerically stable circulatory memory CD8 T cells are defined by the age of memory CD8 T cell (or time after initial antigen-encounter). In addition, history of antigen stimulations has a profound effect on memory CD8 T cell populations, suggesting that repeated infections (or vaccination) have the capacity to further shape the memory CD8 T cell pool. Finally, genetic background of hosts and history of exposure to diverse microorganisms likely contribute to the observed heterogeneity in the memory CD8 T cell compartment. Extending our tool box and exploring alternative mouse models (i.e., "dirty" and/or outbred mice) to encompass and better model diversity observed in humans will remain an important goal for the near future that will likely shed new light into the mechanisms that govern biology of memory CD8 T cells.
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页数:10
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