Dermal γδ T cells - A new player in the pathogenesis of psoriasis

被引:40
作者
Cai, Yihua [1 ,2 ]
Fleming, Chris [1 ,2 ,3 ]
Yan, Jun [1 ,2 ,3 ]
机构
[1] Univ Louisville, Dept Med, James Graham Brown Canc Ctr, Louisville, KY 40202 USA
[2] Univ Louisville, Tumor Immunobiol Program, James Graham Brown Canc Ctr, Louisville, KY 40202 USA
[3] Univ Louisville, Sch Med, Dept Microbiol & Immunol, Louisville, KY 40202 USA
基金
新加坡国家研究基金会;
关键词
Psoriasis; Dermal gamma delta T cells; IL-17; HUMAN SKIN; EPIDERMAL HYPERPLASIA; IDENTIFICATION; LYMPHOCYTES; DIFFERENTIATION; POPULATION; MECHANISMS; VULGARIS; ANTIBODY; RECEPTOR;
D O I
10.1016/j.intimp.2013.02.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Psoriasis is considered as a T-cell driven chronic inflammatory skin disease. Both T helper (Th) 1 and Th17 cells have been demonstrated to participate in psoriasis pathogenesis. Recently, a new subset of gamma delta T cells residing in the dermis has been identified. Dermal gamma delta T cells are the major source of interleukin (IL)-17 in the skin upon IL-23 stimulation. More importantly, they are also shown to be involved in psoriasis development. In this review, we focus on this newly discovered cell population both in mice and human, particularly discussing its role in the pathogenesis of psoriasis. The biologic therapeutics targeting dermal gamma delta T cell and its related molecules in the treatment of psoriasis are also included. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:388 / 391
页数:4
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