Fine-tuning of T cell responses during infection

被引:29
作者
Dorhoi, Anca [1 ]
Kaufmann, Stefan H. E. [1 ]
机构
[1] Max Planck Inst Infect Biol, Dept Immunol, D-10117 Berlin, Germany
关键词
GROWTH-FACTOR-BETA; INNATE IMMUNE RECOGNITION; C-TYPE LECTIN; DENDRITIC CELLS; TGF-BETA; TRYPTOPHAN STARVATION; HELPER-CELLS; TH17; CELLS; RECEPTOR; DIFFERENTIATION;
D O I
10.1016/j.coi.2009.07.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
"Everything in excess is opposed to nature" Hippocrates Adequate control of infection relies on development of a tailored immune response according to the requirements of a given infection. This is achieved by the continuous crosstalk between innate and adaptive immunity. Pathogen diversity is deciphered via a plethora of receptors converging signals to adaptor molecules; tissue sites and environment generate additional signals that further influence T cell lineage decisions. Within this continuum of interactions, fine-tuning of the ensuing T cell responses together with plasticity of the committed T cells ensure development of balanced immune responses maintaining homeostasis. This review focuses on the multiple mechanisms that govern T cell differentiation during infection.
引用
收藏
页码:367 / 377
页数:11
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