生物
FOXP3型
细胞溶解
免疫系统
抑制器
细胞生物学
免疫学
体内
调节性T细胞
抗原
细胞
白细胞介素2受体
体外
T细胞
细胞毒性T细胞
基因
遗传学
出处
期刊:Immunity
[Cell Press]
日期:2009-05-01
卷期号:30 (5): 636-645
被引量:1699
标识
DOI:10.1016/j.immuni.2009.04.010
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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