Regulatory T Cells in the Control of Host-Microorganism Interactions

被引:364
作者
Belkaid, Yasmine [1 ]
Tarbell, Kristin [2 ]
机构
[1] NIAID, Mucosal Immun Unit, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NIDDK, Immune Tolerance Sect, Diabet Branch, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
infection; Foxp3; dendritic cells; Treg; HUMAN-IMMUNODEFICIENCY-VIRUS; TOLL-LIKE RECEPTORS; GROWTH-FACTOR-BETA; ANTIVIRAL IMMUNE-RESPONSE; IN-VITRO PROLIFERATION; DENDRITIC CELLS; TGF-BETA; IFN-GAMMA; LEISHMANIA-MAJOR; CUTTING EDGE;
D O I
10.1146/annurev.immunol.021908.132723
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Each microenvironment requires a specific set of regulatory elements that ire finely and constantly tuned to maintain local homeostasis. Various populations of regulatory T cells contribute to the maintenance of this equilibrium and establishment of controlled immune responses. In particular, regulatory T cells limit the magnitude of effector responses, which may result in failure to adequately control infection. However, regulatory T cells also hell) limit collateral tissue damage caused by vigorous antimicrobial immune responses against pathogenic microbes as well as commensals. In this review, we describe various situations in which the balance between regulatory T cells and effector immune functions influence the outcome of host-microorganism coexistence and discuss current hypotheses and points of polemic associated with the origin, target, and antigen specificity of both endogenous and induced regulatory T cells during these interactions.
引用
收藏
页码:551 / 589
页数:39
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