Harnessing the plasticity of CD4+ T cells to treat immune-mediated disease

被引:381
作者
DuPage, Michel
Bluestone, Jeffrey A. [1 ]
机构
[1] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
CYTOKINE GENE-EXPRESSION; HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; TRANSCRIPTION FACTOR FOXP3; ROR-GAMMA-T; REGULATORY T; HELPER T; CUTTING EDGE; TH17; CELLS; FUNCTIONAL-HETEROGENEITY; LYMPHOKINE ACTIVITIES;
D O I
10.1038/nri.2015.18
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+) T cells differentiate and acquire distinct functions to combat specific pathogens but can also adapt their functions in response to changing circumstances. Although this phenotypic plasticity can be potentially deleterious, driving immune pathology, it also provides important benefits that have led to its evolutionary preservation. Here, we review CD4(+) T cell plasticity by examining the molecular mechanisms that regulate it - from the extracellular cues that initiate and drive cells towards varying phenotypes, to the cytosolic signalling cascades that decipher these cues and transmit them into the cell and to the nucleus, where these signals imprint specific gene expression programmes. By understanding how this functional flexibility is achieved, we may open doors to new therapeutic approaches that harness this property of T cells.
引用
收藏
页码:149 / 163
页数:15
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