Memory cytolytic T-lymphocytes: induction, regulation and implications for vaccine design

被引:6
作者
Baz, Adriana [1 ]
Jackson, David C.
Kienzle, Norbert
Kelso, Anne
机构
[1] Queensland Inst Med Res, Cooperat Res Ctr Vaccine Technol, Brisbane, Qld, Australia
[2] Sch Chem, Dept Immunol, Montevideo, Uruguay
[3] Sch Sci, Montevideo, Uruguay
[4] Univ Melbourne, Cooperat Res Ctr Vaccine Technol, Dept Microbiol & Immunol, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
adjuvants; CD8(+) T cells; cross-presentation; cytokines; dendritic cells; differentiation; granzymes; lipopeptides; perforin; T-cell memory; Toll-like receptors; vaccines;
D O I
10.1586/14760584.4.5.711
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 design of vaccines that protect against intracellular infections or cancer remains a challenge. In many cases, immunity depends on the development of antigen-specific memory CD8(+) T-cells that can express cytokines and kill antigen-bearing cells when they encounter the pathogen or tumor. Here, the authors review current understanding of the signals and cells that lead to memory CD8(+) T-cell differentiation, the relationship between the primary CD8(+) T-cell response and the memory response and the regulation of memory CD8(+) T-cell survival and function. The implications of this new knowledge for vaccine design are discussed, and recent progress in the development of lipidated peptide vaccines as a promising approach for vaccination against intracellular infections and cancer is reviewed.
引用
收藏
页码:711 / 723
页数:13
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