医学
杜皮鲁玛
特应性皮炎
贾纳斯激酶
免疫抑制
坏疽性脓皮病
免疫学
阿纳基纳
皮肤病科
疾病
内科学
细胞因子
作者
Megan Newsom,Arjun M. Bashyam,Esther A. Balogh,Steven R. Feldman,Lindsay C. Strowd
出处
期刊:Drugs
[Adis, Springer Healthcare]
日期:2020-06-09
卷期号:80 (11): 1041-1052
被引量:128
标识
DOI:10.1007/s40265-020-01335-7
摘要
Atopic dermatitis (AD) is a prevalent inflammatory skin condition that, depending on its severity, can cause enormous morbidity. Corticosteroids and systemic immunosuppression, traditionally standard of care for difficult-to-treat disease, have many undesirable side effects. The desire for targeted treatments along with an improved understanding of the pathophysiology of AD has spurred the development of novel treatments. In this article, we review promising new treatments and discuss how their targets-IL-13, IL-31, OX40 (CD134), and the Janus kinase family of proteins-participate in the pathogenesis of AD. We review the published phase II and III data for dupilumab, tralokinumab, lebrikizumab, nemolizumab, anti-OX40 antibody, baricitinib, abrocitinib, and upadacitinib. The introduction of new agents may offer new options, but it remains to be seen how narrow-acting agents, like single interleukin inhibitors, will compare in safety and efficacy to broad-acting agents such as JAK inhibitors.
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