Indoleamine 2,3 dioxygenase and metabolic control of immune responses

被引:797
作者
Munn, David H. [1 ]
Mellor, Andrew L. [2 ]
机构
[1] Georgia Hlth Sci Univ, Ctr Canc, Canc Immunol Inflammat & Tolerance Program, Dept Pediat, Augusta, GA 30912 USA
[2] Georgia Hlth Sci Univ, Ctr Canc, Canc Immunol Inflammat & Tolerance Program, Dept Med, Augusta, GA 30912 USA
关键词
REGULATORY T-CELLS; PLASMACYTOID DENDRITIC CELLS; ARYL-HYDROCARBON RECEPTOR; DRAINING LYMPH-NODES; TRANSFER-RNA-SYNTHETASE; TRYPTOPHAN CATABOLISM; TOLERANCE INDUCTION; INTERFERON-GAMMA; 2,3-DIOXYGENASE; IDO;
D O I
10.1016/j.it.2012.10.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sustained access to nutrients is a fundamental biological need, especially for proliferating cells, and controlling nutrient supply is an ancient strategy to regulate cellular responses to stimuli. By catabolizing the essential amino acid TRP, cells expressing the enzyme indoleamine 2,3 dioxygenase (IDO) can mediate potent local effects on innate and adaptive immune responses to inflammatory insults. Here, we discuss recent progress in elucidating how IDO activity promotes local metabolic changes that impact cellular and systemic responses to inflammatory and immunological signals. These recent developments identify potential new targets for therapy in a range of clinical settings, including cancer, chronic infections, autoimmune and allergic syndromes, and transplantation.
引用
收藏
页码:137 / 143
页数:7
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