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特应性皮炎患者在紫外线A1光疗前后细胞因子的基因表达

Gene expression of cytokines in atopic eczema before and after ultraviolet A1 phototherapy.

作者信息

Gambichler T, Kreuter A, Tomi N S, Othlinghaus N, Altmeyer P, Skrygan M

机构信息

Department of Dermatology, Ruhr-University of Bochum, Gudrunstr. 56, D-44791 Bochum, Germany.

出版信息

Br J Dermatol. 2008 May;158(5):1117-20. doi: 10.1111/j.1365-2133.2008.08498.x. Epub 2008 Mar 20.

DOI:10.1111/j.1365-2133.2008.08498.x
PMID:18363757
Abstract

BACKGROUND

Atopic eczema (AE) is a common pruritic and chronically relapsing inflammatory skin disease in which cytokines seem to represent important factors in the pathogenesis.

OBJECTIVES

We aimed to investigate cytokine mRNA expression in the skin of patients with AE who underwent a course of ultraviolet A1 (UVA1) phototherapy.

METHODS

We studied 21 patients diagnosed with extrinsic AE who were treated with a 6-week course of UVA1 phototherapy. Skin biopsies were taken from healthy controls (n=18) and patients with AE at baseline and after the last UVA1 exposure. Quantitative real-time reverse transcriptase-polymerase chain reaction was performed for interleukin (IL)-4, IL-5, IL-10, IL-13 and IL-31.

RESULTS

A significant reduction of the clinical scores was observed after treatment with UVA1. Except for IL-4, cytokine mRNA expression was significantly increased prior to phototherapy when compared with controls. mRNA levels of IL-4 and IL-10 before UVA1 did not significantly differ from levels observed after UVA1. However, a significant decrease of IL-5, IL-13 and IL-31 mRNA expression was observed following UVA1 treatment. IL-31 mRNA levels were even adjusted to the levels of healthy controls.

CONCLUSIONS

We have shown that the resolution of extrinsic AE lesions following phototherapy is accompanied by significant reduction of mRNA expression of IL-5, IL-13 and IL-31, supporting current concepts that these cytokines play a crucial role in the pathogenesis of extrinsic AE and possibly represent targets for phototherapy.

摘要

背景

特应性皮炎(AE)是一种常见的瘙痒性慢性复发性炎症性皮肤病,细胞因子似乎是其发病机制中的重要因素。

目的

我们旨在研究接受紫外线A1(UVA1)光疗疗程的AE患者皮肤中的细胞因子mRNA表达。

方法

我们研究了21例被诊断为外源性AE的患者,他们接受了为期6周的UVA1光疗。在基线时以及最后一次UVA1照射后,从健康对照者(n = 18)和AE患者身上获取皮肤活检样本。对白细胞介素(IL)-4、IL-5、IL-10、IL-13和IL-31进行定量实时逆转录聚合酶链反应。

结果

用UVA1治疗后观察到临床评分显著降低。与对照组相比,除IL-4外,光疗前细胞因子mRNA表达显著增加。UVA1治疗前IL-4和IL-10的mRNA水平与UVA1治疗后观察到的水平无显著差异。然而,UVA1治疗后观察到IL-5、IL-13和IL-31的mRNA表达显著降低。IL-31的mRNA水平甚至调整到了健康对照者的水平。

结论

我们已经表明,光疗后外源性AE皮损的消退伴随着IL-5、IL-13和IL-31的mRNA表达显著降低,支持了当前的观点,即这些细胞因子在外源性AE的发病机制中起关键作用,并且可能是光疗的靶点。

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