Tissue resident regulatory T cells: novel therapeutic targets for human disease

被引:43
|
作者
Zhou, Xiaohui [1 ,2 ]
Tang, Jiayou [3 ]
Cao, Hao [3 ]
Fan, Huimin [1 ,2 ,3 ]
Li, Bin [4 ]
机构
[1] Tongji Univ, Sch Med, Shanghai East Hosp, Res Ctr Translat Med, Shanghai 200120, Peoples R China
[2] Shanghai Heart Failure Res Ctr, Shanghai 200120, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai East Hosp, Dept Heart Failure, Shanghai 200120, Peoples R China
[4] Shanghai Inst Biol Sci, Inst Pasteur Shanghai, Unit Mol Immunol, Key Lab Mol Virol & Immunol, Shanghai 200120, Peoples R China
基金
上海市科技启明星计划; 中国国家自然科学基金;
关键词
Regulatory T cells; Tissue Tregs; VAT Tregs; Muscle Repair; Areg; Tumor; Bone; Skin memory Tregs; ENDOTHELIAL GROWTH-FACTOR; SUPPRESSIVE FUNCTION; TUMOR ANGIOGENESIS; INSULIN-RESISTANCE; PPAR-GAMMA; UNIQUE POPULATION; FOXP3; EXPRESSION; IMMUNE-SYSTEM; CUTTING EDGE; TH17; CELLS;
D O I
10.1038/cmi.2015.23
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Over the past decade, the ability of regulatory T cells (Tregs) to suppress multiple types of immune cells has received tremendous attention. Mounting evidence has revealed that tissue resident Tregs control non-immunological processes of their target tissues and contribute to a plethora of human diseases. The identification of novel tissue-specific Tregs has highlighted their heterogeneity and complexity. This review summarizes the recent findings for visceral adipose tissue CD4+Foxp3+ regulatory T cells (VAT Tregs), muscle Tregs, bone Tregs and skin memory Tregs, with a focus on their unique functions in local tissues. This interpretation of the roles of tissue-specific Tregs and of their involvement in disease progression provides new insight into the discovery of potential therapeutic targets of human diseases.
引用
收藏
页码:543 / 552
页数:10
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