Autophagy in CD4+ T-cell immunity and tolerance

被引:43
|
作者
Luenemann, J. D. [1 ]
Muenz, C. [1 ]
机构
[1] Rockefeller Univ, Christopher H Browne Ctr Immunol & Immune Dis, Lab Viral Immunobiol, New York, NY 10021 USA
来源
CELL DEATH AND DIFFERENTIATION | 2009年 / 16卷 / 01期
基金
美国国家卫生研究院;
关键词
autophagy; immunity; MHC; T cell; MHC CLASS-II; GENOME-WIDE ASSOCIATION; RESTRICTED PRESENTATION; CYTOSOLIC ANTIGEN; DENDRITIC CELLS; IN-VIVO; CYTOPLASMIC ANTIGENS; ENDOGENOUS PROTEINS; EPITHELIAL-CELLS; NUCLEAR ANTIGEN;
D O I
10.1038/cdd.2008.113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy is a homeostatic process that enables eukaryotic cells to deliver cytoplasmic constituents for lysosomal degradation, to recycle nutrients and to survive during starvation. In addition to these primordial functions, autophagy has emerged as a key mechanism in orchestrating innate and adaptive immune responses to intracellular pathogens. Autophagy restricts viral infections as well as replication of intracellular bacteria and parasites and delivers pathogenic determinants for TLR stimulation and for MHC class II presentation to the adaptive immune system. Apart from its role in defense against pathogens, autophagy-mediated presentation of self-antigens in the steady state could have a crucial role in the induction and maintenance of CD4(+) T-cell tolerance. This review describes the mechanisms by which the immune system utilizes autophagic degradation of cytoplasmic material to regulate adaptive immune responses.
引用
收藏
页码:79 / 86
页数:8
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