人类白癜风小鼠模型

Q2 Immunology and Microbiology
Rebecca L. Riding, Jillian M. Richmond, John E. Harris
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引用次数: 26

摘要

白癜风是一种自身免疫性皮肤病,其中产生色素的黑色素细胞被自身反应性CD8+ T细胞破坏。结果,患者的皮肤上出现了难看的白斑。本文讨论了第一个白癜风小鼠模型,其表皮色素沉着,类似于人类患者的疾病。为了实现表皮脱色,通过基因工程使小鼠的皮肤表皮保留黑素细胞。通过将黑色素细胞特异性CD8+ T细胞过继转移到受体小鼠中,然后使用病毒载体激活这些T细胞,可以诱导疾病。表皮色素脱色在5至7周内发生,呈斑片状,与白癜风患者相似。本文介绍了白癜风诱导的方法,病变进展和消退的量化,皮肤处理进行详细分析,以及如何使用该模型为临床研究提供信息。©2018 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mouse Model for Human Vitiligo

Mouse Model for Human Vitiligo

Mouse Model for Human Vitiligo

Mouse Model for Human Vitiligo

Vitiligo is an autoimmune skin disease in which the pigment-producing melanocytes are destroyed by autoreactive CD8+ T cells. As a result, patients develop disfiguring white spots on the skin. This article discusses the first mouse model of vitiligo that develops epidermal depigmentation, similar to disease in human patients. To achieve epidermal depigmentation, mice are genetically engineered to retain melanocytes in the skin epidermis. Induction of disease occurs by adoptive transfer of melanocyte-specific CD8+ T cells into recipient mice and the subsequent activation of these T cells using a viral vector. Depigmentation of the epidermis occurs within 5 to 7 weeks in a patchy pattern similar to patients with vitiligo. This article describes the methods of vitiligo induction, quantification of lesion progression and regression, processing of the skin for detailed analysis, and how to use this model to inform clinical studies. © 2018 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Immunology
Current Protocols in Immunology Immunology and Microbiology-Immunology
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