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特应性皮炎复发现象期间IgE、IgG4及Th2细胞细胞因子产生的选择性增强及甲苯磺酸舒他西林的预防作用

Selective enhancement of production of IgE, IgG4, and Th2-cell cytokine during the rebound phenomenon in atopic dermatitis and prevention by suplatast tosilate.

作者信息

Kimata H

机构信息

Department of Allergy, Unitika Central Hospital, Uji-City, Kyoto Prefecture, Japan.

出版信息

Ann Allergy Asthma Immunol. 1999 Mar;82(3):293-5. doi: 10.1016/S1081-1206(10)62611-7.

Abstract

BACKGROUND

Atopic dermatitis is a chronic inflammatory skin disease, which is commonly treated with topical steroids. It is, however, associated with rebound after therapy has been discontinued.

OBJECTIVE

This study was designed to elucidate the mechanisms of the rebound phenomenon, and to test the effect of an oral anti-allergic medication, suplatast tosilate, on atopic dermatitis.

METHODS

This is a randomized, placebo controlled study. Patients with atopic dermatitis who had been treated with strong steroid ointment (dexamethasone valerate) for several years were divided into two groups. One group (the control group, n = 15) was treated with a non-steroid anti-inflammatory ointment (bufexamac ointment), while the other group (the suplatast tosilate group, n = 17) was treated with the anti-allergic medications, suplatast tosilate and bufexamac ointment. In each group, in vitro production of immunoglobulins and cytokines before and after 2 weeks of treatment was measured.

RESULTS

In the control group, 15 of the 15 patients experienced rebound and mean production of IgE, IgG4, IL-4, IL-5, IL-10, and IL-13 was enhanced after 2 weeks. In contrast, only 2 of the 17 patients in the suplatast tosilate group experienced rebound. There was no enhancement of production of immunoglobulins and cytokines after 2 weeks of treatment.

CONCLUSION

Enhanced production of the Th2-cell cytokines, which selectively induces IgE and IgG4 production, may be involved in the pathogenesis of the rebound phenomenon, and that suplatast tosilate may prevent the rebound phenomenon by down-regulating the production of these cytokines.

摘要

背景

特应性皮炎是一种慢性炎症性皮肤病,通常用外用类固醇治疗。然而,在治疗中断后会出现反弹。

目的

本研究旨在阐明反弹现象的机制,并测试口服抗过敏药物甲苯磺酸舒普拉泰对特应性皮炎的疗效。

方法

这是一项随机、安慰剂对照研究。将使用强效类固醇软膏(戊酸倍他米松)治疗数年的特应性皮炎患者分为两组。一组(对照组,n = 15)用非甾体抗炎软膏(丁苯羟酸软膏)治疗,另一组(甲苯磺酸舒普拉泰组,n = 17)用抗过敏药物甲苯磺酸舒普拉泰和丁苯羟酸软膏治疗。每组在治疗2周前后测量免疫球蛋白和细胞因子的体外产生情况。

结果

对照组的15名患者均出现反弹,2周后IgE、IgG4、IL-4、IL-5、IL-10和IL-13的平均产生量增加。相比之下,甲苯磺酸舒普拉泰组的17名患者中只有2名出现反弹。治疗2周后免疫球蛋白和细胞因子的产生没有增加。

结论

选择性诱导IgE和IgG4产生的Th2细胞细胞因子产生增加可能与反弹现象的发病机制有关,甲苯磺酸舒普拉泰可能通过下调这些细胞因子的产生来预防反弹现象。

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