Molecular regulation of effector and memory T cell differentiation

被引:432
作者
Chang, John T. [1 ]
Wherry, E. John [2 ,3 ]
Goldrath, Ananda W. [4 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Penn, Perelman Sch Med, Inst Immunol, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
[4] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
FOLLICULAR HELPER-CELL; RESIDENT MEMORY; TRANSCRIPTION FACTOR; GENE-EXPRESSION; CUTTING EDGE; SELECTIVE EXPRESSION; BICOID PROTEIN; CD8(+); TISSUE; BATF;
D O I
10.1038/ni.3031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunological memory is a cardinal feature of adaptive immunity and an important goal of vaccination strategies. Here we highlight advances in the understanding of the diverse T lymphocyte subsets that provide acute and long-term protection from infection. These include new insights into the transcription factors, and the upstream 'pioneering' factors that regulate their accessibility to key sites of gene regulation, as well as metabolic regulators that contribute to the differentiation of effector and memory subsets; ontogeny and defining characteristics of tissue-resident memory lymphocytes; and origins of the remarkable heterogeneity exhibited by activated T cells. Collectively, these findings underscore progress in delineating the underlying pathways that control diversification in T cell responses but also reveal gaps in the knowledge, as well as the challenges that arise in the application of this knowledge to rationally elicit desired T cell responses through vaccination and immunotherapy.
引用
收藏
页码:1104 / 1115
页数:12
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