Shaping and reshaping CD8+ T-cell memory

被引:453
作者
Harty, John T. [1 ]
Badovinac, Vladimir P. [2 ]
机构
[1] Univ Iowa, Grad Program Immunol, Dept Microbiol & Interdisciplinary, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nri2251
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ability to develop and sustain populations of memory T cells after infection or immunization is a hallmark of the adaptive immune response and a basis for protective vaccination against infectious disease. Technical advances that allow direct ex vivo identification and characterization of antigen-specific CD8(+) T cells at various stages of the response to infection or vaccination in mouse models have fuelled efforts to characterize the factors that control memory CD8(+) T-cell generation. Here, we dissect the input signals that shape the characteristics of the memory CD8(+) T-cell response and discuss how manipulation of these signals has the potential to reshape CD8(+) T-cell memory and improve the efficacy of vaccination.
引用
收藏
页码:107 / 119
页数:13
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