白癜风
发病机制
生物
免疫学
医学
细胞毒性T细胞
脱色
趋化因子
CD8型
免疫系统
疾病
遗传学
病理
体外
作者
Michael L. Frisoli,Kingsley I. Essien,John E. Harris
出处
期刊:Annual Review of Immunology
[Annual Reviews]
日期:2020-02-04
卷期号:38 (1): 621-648
被引量:306
标识
DOI:10.1146/annurev-immunol-100919-023531
摘要
Vitiligo is an autoimmune disease of the skin that targets pigment-producing melanocytes and results in patches of depigmentation that are visible as white spots. Recent research studies have yielded a strong mechanistic understanding of this disease. Autoreactive cytotoxic CD8 + T cells engage melanocytes and promote disease progression through the local production of IFN-γ, and IFN-γ-induced chemokines are then secreted from surrounding keratinocytes to further recruit T cells to the skin through a positive-feedback loop. Both topical and systemic treatments that block IFN-γ signaling can effectively reverse vitiligo in humans; however, disease relapse is common after stopping treatments. Autoreactive resident memory T cells are responsible for relapse, and new treatment strategies focus on eliminating these cells to promote long-lasting benefit. Here, we discuss basic, translational, and clinical research studies that provide insight into the pathogenesis of vitiligo, and how this insight has been utilized to create new targeted treatment strategies.
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