Treating atopic dermatitis at the source: corrective barrier repair therapy based upon new pathogenic insights

P. Elias, R. Sun, J. Wakefield, M. Man
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引用次数: 19

Abstract

Until recently, atopic dermatitis (AD) has been linked to Th1/Th2 cell dysregulation. But now, the opinion that inflammation in AD results from a convergence of inherited and acquired insults to the cutaneous permeability barrier, with variable contributions from inherited abnormalities in innate/adaptive immunity, is becoming increasingly accepted. Current therapy is however, still largely directed towards ameliorating immunologically triggered inflammation, rather than correcting the barrier abnormality. In this article, the authors provide an overview of epidermal barrier function; a review of recent molecular genetic studies pointing to a primary barrier abnormality in AD; a detailed description of new pathogenic insights into AD; and they compare the efficacy of several putative ‘barrier repair’ products currently utilized as adjunctive or primary therapy for AD. The authors also explore the potential of ‘next-generation’ barrier repair approaches that attack specific pathogenic mechanisms in AD (hig...
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从源头上治疗特应性皮炎:基于新的致病见解的纠正性屏障修复疗法
直到最近,特应性皮炎(AD)一直被认为与Th1/Th2细胞失调有关。但是现在,越来越多的人认为,AD中的炎症是由于遗传和获得性对皮肤渗透性屏障的损害,以及先天/适应性免疫的遗传异常的不同贡献,这一观点越来越被接受。然而,目前的治疗仍然主要是针对改善免疫引发的炎症,而不是纠正屏障异常。在本文中,作者提供了表皮屏障功能的概述;最近的分子遗传学研究综述指出阿尔茨海默病的原发性屏障异常;对阿尔茨海默病病原学新见解的详细描述;他们比较了目前用作AD辅助或主要治疗的几种假定的“屏障修复”产品的疗效。作者还探索了“下一代”屏障修复方法的潜力,这些方法可以攻击阿尔茨海默病的特定致病机制。
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