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免疫组织化学研究 Toll 样受体 1 和 2 在皮肤扁平苔藓病变中的表达。

Immunohistochemical study of Toll-like receptors 1 and 2 expression in cutaneous lichen planus lesions.

机构信息

Dermatology and Venereology Department, Faculty of Medicine, Ain Shams University, Abbasseya Square, Cairo, Egypt.

出版信息

Arch Dermatol Res. 2013 Mar;305(2):125-31. doi: 10.1007/s00403-012-1267-8. Epub 2012 Jul 28.

DOI:10.1007/s00403-012-1267-8
PMID:22842950
Abstract

Lichen planus (LP) is a chronic inflammatory, T cell-mediated autoimmune skin disease. Innate immunity could explain the interplay between environmental triggers and the autoimmune cascade leading to disease development. Toll-like receptors (TLRs) are important components of the innate immune system, with no previous evaluation of TLRs 1 and 2 in cutaneous LP. This work aims to investigate TLRs 1 and 2 expression in cutaneous LP. This case-control study included 30 patients with LP and 15 healthy controls. Biopsies from the patients' lesional skin and from the controls' normal skin were examined immunohistochemically for TLR 1 and 2 expression. A significant re-localization was found in TLR1 expression with a higher percentage of basal and a significantly lower percentage of homogenous epidermal expression in patients (73.3 and 0 %, respectively) compared with controls (13.3 and 73.3 %, respectively) (P < 0.001). TLR2 showed a significantly higher percentage of epidermal expression (more in the upper spinous layer) and significantly lower percentage of epidermal but more basal expression in patients (66.6 and 10 %, respectively) compared with controls (0 and 73.3 %, respectively) (P < 0.001). The median (IQR) of TLR1 [1 (0.75-1)] and TLR2 [1 (1-1)] staining score in patients was significantly lower than that of the controls [2 (1-2) and 1 (1-2), respectively] (P < 0.05). This work thus shows a re-localization of TLR 1 and 2 expression sites with decreased grade of expression in LP lesions. Targeting TLR signaling is expected to be a novel treatment strategy for cutaneous LP.

摘要

扁平苔藓(LP)是一种慢性炎症性、T 细胞介导的自身免疫性皮肤病。先天免疫可以解释环境触发因素与导致疾病发展的自身免疫级联之间的相互作用。Toll 样受体(TLR)是先天免疫系统的重要组成部分,以前尚未评估过皮肤 LP 中的 TLR1 和 TLR2。这项工作旨在研究 TLR1 和 TLR2 在皮肤 LP 中的表达。这项病例对照研究包括 30 名 LP 患者和 15 名健康对照者。对患者皮损皮肤和对照者正常皮肤的活检标本进行 TLR1 和 TLR2 表达的免疫组织化学检查。与对照组相比,患者的 TLR1 表达有明显的重新定位,基底细胞的表达比例较高,而均匀表皮的表达比例显著较低(分别为 73.3%和 0%)(P<0.001)。TLR2 表现出明显较高的表皮表达比例(在上棘状层更多),而患者的表皮和基底表达比例明显较低(分别为 66.6%和 10%)(P<0.001)。与对照组相比,患者的 TLR1[1(0.75-1)]和 TLR2[1(1-1)]染色评分中位数(IQR)明显较低[2(1-2)和 1(1-2)](P<0.05)。因此,本研究显示 LP 病变中 TLR1 和 TLR2 表达部位的重新定位,表达水平降低。靶向 TLR 信号可能是治疗皮肤 LP 的一种新策略。

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