窄带UVB治疗白癜风患者细胞免疫功能的改变。

N. F. Ibrahim, Nashwa K. Radwan, L. Rashed
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引用次数: 0

摘要

白癜风被认为是一种自身免疫性脱色疾病。许多证据表明,T细胞介导的免疫和细胞因子在该病的发病机制中起着重要作用。研究纳入20例活动期白癜风患者(1组)、20例窄带紫外线B (NBUVB)治疗患者(2组)和20例年龄、性别匹配的健康对照(3组)。采用ELISA技术检测三组患者皮肤组织中IL- 17、IL-10、TGF- Bi水平。结果显示,与对照组相比,活动期白癜风患者IL- 17和TGF-Bi显著升高,IL-10显著降低(P= 0.000)。NB-UVB治疗后,与活动期白癜风组相比,IL- 17和TGF-Bi水平均显著降低,IL-10水平显著升高(P= 0.000)。这些具有统计学意义的结果表明,细胞介导的免疫作用在疾病中起作用,而窄波段UVB的成功治疗改变了细胞因子的毒性作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alteration of Cell Mediated Immunity in Vitiligo Patients Using Narrow Band UVB as a Treatment.
VITILIGO is considered an autoimmune depigmenting disease. There were many evidences suggested the role of T cell mediated immunity and cytokines in the pathogenesis of the disease. The study included 20 active vitiligo patients (group 1), 20 treated patients using narrow band ultraviolet radiation B (NBUVB) (group 2), and 20 healthy control of matching age and sex (group 3). IL- 17, IL-10, TGF- Bi levels in skin tissue were measured in the three groups using ELISA technique. The results showed a significant increase in IL- 17 and TGF-Bi while there was a significant decrease in IL-10 in active vitiligo patients compared to the control (P= 0.000). Following treatment using NB-UVB, the results showed a significant decrease in the level of both IL- 17 and TGF-Bi while there was a significant increase in IL-10 (P= 0.000) compared to active vitiligo group. These statistically significant results suggest the cell mediated immune role in the disease and successful treatment by the narrow band UVB that altered the cytokines toxic effect.
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