Dupilumab for Moderate-to-Severe Atopic Dermatitis.

Q1 Medicine
Skin therapy letter Pub Date : 2017-11-01
R Vangipuram, S K Tyring
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引用次数: 0

Abstract

Atopic dermatitis (AD) is the most common chronic inflammatory disease affecting 2-10% of adults and up to 15-30% of children. Despite a rising prevalence, effective and safe therapeutics for patients with moderate-to-severe AD are limited due to toxicity and side effects. Dupilumab, an interleukin (IL)-4 and IL-13 antagonist that limits type 2 T helper (Th2) driven inflammatory activity, is a promising therapeutic option. In clinical trials, it has demonstrated efficacy by reducing clinical activity and symptoms, and showed improvement in the AD genomic phenotype, including a significant reduction in Th2 chemokines and reversal of key epidermal markers of AD. It also has a favorable safety profile. This review discusses the role of dupilumab in treating Th2 related inflammation, and its efficacy and safety, as demonstrated in clinical trials. Dupilumab (Dupixent®) recently gained US FDA approval for patients with moderate-to-severe AD, and is poised to revolutionize the management of this chronic, relapsing condition.

Dupilumab用于中重度特应性皮炎。
特应性皮炎(AD)是最常见的慢性炎症性疾病,影响2-10%的成年人和高达15-30%的儿童。尽管患病率不断上升,但由于毒性和副作用,对中重度AD患者有效和安全的治疗方法有限。Dupilumab是一种白细胞介素(IL)-4和IL-13拮抗剂,可限制2型T辅助(Th2)驱动的炎症活性,是一种很有前景的治疗选择。在临床试验中,它通过降低临床活动和症状证明了疗效,并显示了AD基因组表型的改善,包括Th2趋化因子的显著降低和AD关键表皮标志物的逆转。它还具有良好的安全性。这篇综述讨论了dupilumab在治疗Th2相关炎症中的作用,以及临床试验证明的dupilumab的有效性和安全性。Dupilumab (Dupixent®)最近获得了美国FDA批准用于中重度AD患者,并准备彻底改变这种慢性复发性疾病的管理。
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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来源期刊
Skin therapy letter
Skin therapy letter Medicine-Medicine (all)
CiteScore
2.80
自引率
0.00%
发文量
0
期刊介绍: The premier international journal on the latest advances, techniques and practice in conservation and restoration from around the world.
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