An Appropriate Response to the Black-Box Warning: Corrective, Barrier Repair Therapy in Atopic Dermatitis.

Clinical medicine. Dermatology Pub Date : 2009-02-09
Peter M Elias
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Abstract

Due to years of sophisticated research on T cell function, many dermatologists have viewed atopic dermatitis (AD) largely as an inflammatory disorder of TH1/TH2 imbalance. Hence, therapy has largely consisted of topical immunomodulators and/or steroids. The imposition of "black box" warnings about the potential toxicity associated with prolonged use of the immunosuppressive drugs, tacrolimus 0.1% or 0.3% ointment (Protopic((R)), Astellas Pharma U.S., Inc., Deerfield, IL) and pimecrolimus 1% cream (Elidel((R)), Novartis, Basel, Switzerland), as well as legitimate concerns about the adverse side effects of potent topical steroids, has stimulated a search for alternate forms of therapy. Recent genetic studies point to the primary role of a defective barrier to water loss and microbial invasion in the provocation of AD, creating a rationale for 'barrier repair' therapy. This approach utilizes topical applications of specific combination of the three (3) epidermal lipids that comprise the epidermal permeability barrier in a ratio (ceramide-dominant) that corrects the biochemical abnormality in AD.1,2 We review here both recent concerns about the topical immunomodulators, as well as the rationale for barrier repair therapy.

对黑盒警告的适当回应:纠正性屏障修复治疗特应性皮炎。
由于多年来对T细胞功能的复杂研究,许多皮肤科医生将特应性皮炎(AD)主要视为TH1/TH2失衡的炎症性疾病。因此,治疗主要由局部免疫调节剂和/或类固醇组成。长期使用免疫抑制药物0.1%或0.3%他克莫司软膏(Protopic(R), Astellas Pharma us, Inc., Deerfield, IL)和1%吡美莫司乳膏(Elidel(R), Novartis, Basel, Switzerland)的潜在毒性的“黑盒子”警告的强制实施,以及对强效外用类固醇的不良副作用的合理担忧,刺激了对替代治疗形式的研究。最近的遗传学研究指出,在阿尔茨海默病的诱发过程中,防止水分流失和微生物入侵的屏障缺陷发挥了主要作用,为“屏障修复”疗法创造了基本原理。这种方法利用局部应用三(3)种表皮脂质的特定组合,它们组成表皮渗透性屏障,以一定比例(神经酰胺占主导地位)纠正ad中的生化异常。我们在这里回顾了最近对局部免疫调节剂的关注,以及屏障修复治疗的基本原理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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