How Tolerogenic Dendritic Cells Induce Regulatory T Cells

被引:330
作者
Maldonado, Roberto A. [1 ]
von Andrian, Ulrich H. [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Immune Dis Inst, Boston, MA 02115 USA
来源
ADVANCES IN IMMUNOLOGY, VOL 108 | 2010年 / 108卷
关键词
VASOACTIVE-INTESTINAL-PEPTIDE; VERSUS-HOST-DISEASE; TRANSCRIPTION FACTOR FOXP3; GROWTH-FACTOR-BETA; ANTIGEN-SPECIFIC TOLERANCE; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; COLONY-STIMULATING FACTOR; NECROSIS-FACTOR-ALPHA; DRAINING LYMPH-NODES; KAPPA-B ACTIVATION;
D O I
10.1016/S0065-2776(10)08004_1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since their discovery by Steinman and Cohn in 1973 dendritic cells (DCs) have become increasingly recognized for their crucial role as regulators of innate and adaptive immunity DCs are exquisitely adept at acquiring processing and presenting antigens to T cells They also adjust the context (and hence the outcome) of antigen presentation in response to a plethora of environmental inputs that signal the occurrence of pathogens or tissue damage Such signals generally boost DC maturation which promotes their migration from peripheral tissues into and within secondary lymphoid organs and their capacity to induce and regulate effector T cell responses Conversely more recent observations indicate that DCs are also crucial to ensure immunological peace Indeed DCs constantly present innocuous self- and nonself-antigens in a fashion that promotes tolerance at least in part through the control of regulatory T cells (Tregs) Tregs are specialized T cells that exert their immunosuppressive function through a variety of mechanisms affecting both DCs and effector cells Here we review recent advances in our understanding of the relationship between tolerogenic DCs and Tregs
引用
收藏
页码:111 / 165
页数:55
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