Yang Lili, Wei Yi, Sun Yue, Shi Weimin, Yang Ji, Zhu Lubing, Li Ming
Department of Dermatology, Zhongshan Hospital, Fudan University, Shanghai, China.
Acta Derm Venereol. 2015 Jul;95(6):664-70. doi: 10.2340/00015555-2080.
Increased expression of the cytokine interferon (IFN)-γ plays a pivotal role in vitiligo-induced depigmentation. However, the major source of IFN-γ in vitiligo patients and the mechanisms underlying melanocyte destruction are unknown. In this study, a large number of skin infiltrating IFN-γ+ cells and CD8+ T cells were detected in progressive vitiligo. Among the peripheral blood mononuclear cells (PBMCs) of vitiligo patients, CD8+ cytotoxic T lymphocytes (CTLs) that express IFN-γ exhibited significant expansion, which suggests that activated CTLs are the main source of increased IFN-γ in progressive vitiligo. An in vitro analysis demonstrated that IFN-γ inhibits melanogenesis in primary cultured human melanocytes by altering melanogenic enzyme mRNA expression and, more importantly, that IFN-γ directly induces melanocyte apoptosis. Our data indicate that vitiligo pathophysiology may be linked to globally activated CD8+ CTL subpopulations, which produce increased IFN-γ and induce melanocyte dysfunction and apoptosis.
细胞因子干扰素(IFN)-γ表达增加在白癜风所致色素脱失中起关键作用。然而,白癜风患者中IFN-γ的主要来源以及黑素细胞破坏的潜在机制尚不清楚。在本研究中,在进展期白癜风中检测到大量皮肤浸润的IFN-γ+细胞和CD8+ T细胞。在白癜风患者的外周血单个核细胞(PBMC)中,表达IFN-γ的CD8+细胞毒性T淋巴细胞(CTL)显著扩增,这表明活化的CTL是进展期白癜风中IFN-γ增加的主要来源。体外分析表明,IFN-γ通过改变黑素生成酶mRNA表达抑制原代培养的人黑素细胞中的黑素生成,更重要的是,IFN-γ直接诱导黑素细胞凋亡。我们的数据表明,白癜风的病理生理学可能与整体活化的CD8+ CTL亚群有关,该亚群产生增加的IFN-γ并诱导黑素细胞功能障碍和凋亡。