Regulatory T cells in autoimmune disease

被引:494
|
作者
Dominguez-Villar, Margarita [1 ]
Hafler, David A. [1 ,2 ]
机构
[1] Yale Sch Med, Dept Neurol, New Haven, CT 06510 USA
[2] Yale Sch Med, Dept Immunobiol, New Haven, CT 06510 USA
关键词
TRANSCRIPTION FACTOR FOXP3; TH1-LIKE TREG GENERATION; SUPPRESSIVE FUNCTION; NEONATAL THYMECTOMY; FUNCTIONAL DEFECT; SELF-TOLERANCE; HELPER-CELLS; CIS-ELEMENT; PPAR-GAMMA; TH17; CELLS;
D O I
10.1038/s41590-018-0120-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In recent years, the understanding of regulatory T cell (Treg cell) biology has expanded considerably. Key observations have challenged the traditional definition of Treg cells and have provided insight into the underlying mechanisms responsible for the development of autoimmune diseases, with new therapeutic strategies that improve disease outcome. This Review summarizes the newer concepts of Treg cell instability, Treg cell plasticity and tissue-specific Treg cells, and their relationship to autoimmunity. Those three main concepts have changed the understanding of Treg cell biology: how they interact with other immune and nonimmune cells; their functions in specific tissues; and the implications of this for the pathogenesis of autoimmune diseases.
引用
收藏
页码:665 / 673
页数:9
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