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白癜风患者皮肤中抗菌肽(LL-37)免疫表达的研究。

Study of cathelicidin (LL-37) immunoexpression in the skin of vitiligo patients.

作者信息

Elgarhy Lamia Hamouda, Ramadan Basma Ramadan Refaey, Sallam Fersan Abd Allah, Iskandarani Dalya Ayman, Hewedy El-Sayed Shaaban

机构信息

Dermatology and Venereology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

Pathology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

出版信息

Arch Dermatol Res. 2025 Jan 28;317(1):316. doi: 10.1007/s00403-025-03801-2.

Abstract

Vitiligo is a pigmentary disorder acquired and caused by the loss or destruction of melanocytes from the epidermis. There is strong proof that vitiligo is mainly an autoimmune disease. Cathelicidin (LL37), an antimicrobial polypeptide, is an important part of the innate immune system and has a role in different skin autoimmune diseases. The present work aimed to study the immunoexpression of cathelicidin in the vitiligo patients' skin to elucidate its possible role in vitiligo pathogenesis. Twenty vitiligo patients and 20 controls of matched sex and age were included. A 3 mm punch biopsy was taken from the non-lesional and lesional skin of each patient and controlled subjects. Each was stained with hematoxylin and eosin (H&E) and subjected to cathelicidin immunostaining detection. A significant difference was detected between the two studied groups regarding cathelicidin immunohistochemical expression (Pvalue < 0.001). The lesional immunohistochemical expression of cathelicidin showed a mean of 2.85 ± 0.67. The non-lesional immunohistochemical expression of cathelicidin showed a mean of 2.05 ± 0.51 with a statistically significant higher mean value in the patients' group than the controls (P < 0.001) which recommends that cathelicidin may play a role in the vitiligo pathogenesis. The immunohistochemical scores of the lesional and non-lesional cathelicidin levels were significantly related to the VIDA score (p < 0.001 and = 0.016, respectively) which suggests a role of cathelicidin in vitiligo activity. A significant elevation was indicated in the non-lesional cathelicidin expression, indicating that cathelicidin may be able to predict the appearance of future lesions in non-lesional skin, this requires further longitudinal studies to be confirmed.

摘要

白癜风是一种后天获得的色素沉着紊乱疾病,由表皮黑素细胞的丧失或破坏引起。有强有力的证据表明,白癜风主要是一种自身免疫性疾病。抗菌多肽cathelicidin(LL37)是先天免疫系统的重要组成部分,在不同的皮肤自身免疫性疾病中发挥作用。本研究旨在探讨cathelicidin在白癜风患者皮肤中的免疫表达,以阐明其在白癜风发病机制中的可能作用。研究纳入了20名白癜风患者和20名年龄和性别匹配的对照者。从每位患者和对照者的非皮损区和皮损区皮肤取3毫米的打孔活检组织。每块组织进行苏木精-伊红(H&E)染色,并进行cathelicidin免疫染色检测。在cathelicidin免疫组化表达方面,两个研究组之间检测到显著差异(P值<0.001)。cathelicidin的皮损免疫组化表达平均值为2.85±0.67。cathelicidin的非皮损免疫组化表达平均值为2.05±0.51,患者组的平均值在统计学上显著高于对照组(P<0.001),这表明cathelicidin可能在白癜风发病机制中起作用。皮损和非皮损区cathelicidin水平的免疫组化评分与白癜风疾病活动评分(VIDA评分)显著相关(分别为p<0.001和=0.016),这表明cathelicidin在白癜风活动中起作用。非皮损区cathelicidin表达有显著升高,表明cathelicidin可能能够预测非皮损区皮肤未来皮损的出现,这需要进一步的纵向研究来证实。

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