共 67 条
Mechanisms of Foxp3+ T Regulatory Cell-Mediated Suppression
被引:1457
作者:

Shevach, Ethan M.
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Immunol Lab, Natl Inst Hlth, Bethesda, MD 20892 USA NIAID, Immunol Lab, Natl Inst Hlth, Bethesda, MD 20892 USA
机构:
[1] NIAID, Immunol Lab, Natl Inst Hlth, Bethesda, MD 20892 USA
来源:
关键词:
DENDRITIC CELLS;
TGF-BETA;
CUTTING EDGE;
AUTOIMMUNE-DISEASE;
IN-VITRO;
GRANZYME-B;
EFFECTOR;
ACTIVATION;
EXPRESSION;
TOLERANCE;
D O I:
10.1016/j.immuni.2009.04.010
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Foxp3(+) T regulatory (Treg) cells control all aspects of the immune response. Here, I will review the in vitro model systems that have been developed to define the mechanisms used by Treg cells to suppress a large number of distinct target cell types. These mechanisms can be broadly divided into those that target T cells (suppressor cytokines, IL-2 consumption, cytolysis) and those that primarily target antigen-presenting cells (decreased costimulation or decreased antigen presentation). Although multiple mechanisms for Treg cell suppression have been shown in vitro, it is unclear whether the same or different mechanisms are used by Treg cells in vivo. An increase in our understanding of Treg cell suppressor mechanisms will offer an insight into how Treg cell function can be manipulated either positively or negatively in vivo.
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收藏
页码:636 / 645
页数:10
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