Retinoic acid-dependent regulation of immune responses by dendritic cells and macrophages

被引:114
作者
Manicassamya, Santhakumar [1 ]
Pulendrana, Bali [1 ,2 ]
机构
[1] Yerkes Natl Primate Res Ctr, Emory Vaccine Ctr, Atlanta, GA 30329 USA
[2] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
Macrophages; Retinoic acid; VITAMIN-A-DEFICIENCY; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; T-CELLS; PEYERS PATCH; HIPPOCAMPAL-NEURONS; ANTIBODY-RESPONSES; NERVOUS-SYSTEM; TGF-BETA; IN-VIVO; GUT;
D O I
10.1016/j.smim.2008.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) control the strength and quality of antigen-specific T and B cell responses. Recent advances point to a novel mechanism, in which metabolism of vitamin A into retinoic acid (RA) in DCs, regulate critical parameters of lymphocyte differentiation. First, RA enhances the induction of Foxp3(+) T regulatory cells by DCs. Thus, specific subsets of intestinal DCs and macrophages constitutively express RA synthesizing enzymes, and induce T regulatory cells. In addition, RA programs DCs to imprint mucosal homing properties on activated T and B cells, and enhanced induction of immunoglobulin-A (IgA) by B cells. Here, we review these recent advances, in the context of the pleiotropic effects of RA in regulating diverse biological processes. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 27
页数:6
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