共 23 条
Plasticity of Treg at infected sites
被引:30
作者:

Wohlfert, E.
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Mucosal Immunol Unit, Parasit Dis Lab, Bethesda, MD 20892 USA NIAID, Mucosal Immunol Unit, Parasit Dis Lab, Bethesda, MD 20892 USA

Belkaid, Y.
论文数: 0 引用数: 0
h-index: 0
机构:
NIAID, Mucosal Immunol Unit, Parasit Dis Lab, Bethesda, MD 20892 USA NIAID, Mucosal Immunol Unit, Parasit Dis Lab, Bethesda, MD 20892 USA
机构:
[1] NIAID, Mucosal Immunol Unit, Parasit Dis Lab, Bethesda, MD 20892 USA
关键词:
CELL-DIFFERENTIATION;
FOXP3;
INDUCTION;
D O I:
10.1038/mi.2010.11
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Regulatory T cells (T-reg) control an array of immune responses both in the context of various polarized settings as well as in distinct microenvironments. This implies that maintenance of peripheral homeostasis relies on the capacity of T-reg to appropriately adapt to these defined settings while sustaining a regulatory program in the face of inflammation. Adaptation of T-reg is particularly critical in tissues constantly exposed to microbes, such as the gut or the skin, or in the context of exposure to pathogenic microbes. Recent evidence supports the idea that the capacity of T-reg to control defined polarized settings can be associated with the acquisition of specific transcription factors previously associated with effector T-cell lineages. In this review we will discuss how such adaptation of T-reg can have a major role in the control of host-microbe interaction.
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收藏
页码:213 / 215
页数:3
相关论文
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