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特应性皮炎的新型和新兴系统治疗方法。

New and Emerging Systemic Treatments for Atopic Dermatitis.

机构信息

Department of Dermatology, Center for Dermatology Research, Medical Center Boulevard, Wake Forest School of Medicine, Winston-Salem, North Carolina, 27157-1071, USA.

Department of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, USA.

出版信息

Drugs. 2020 Jul;80(11):1041-1052. doi: 10.1007/s40265-020-01335-7.

Abstract

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.

摘要

特应性皮炎(AD)是一种常见的炎症性皮肤疾病,根据其严重程度,可能会导致巨大的发病率。皮质类固醇和全身性免疫抑制,传统上是治疗难治性疾病的标准治疗方法,但有许多不良副作用。由于人们希望采用靶向治疗以及对 AD 病理生理学的理解的提高,因此刺激了新型治疗方法的发展。在本文中,我们回顾了有前途的新治疗方法,并讨论了它们的靶标(IL-13、IL-31、OX40(CD134)和 Janus 激酶家族蛋白)如何参与 AD 的发病机制。我们回顾了度普利尤单抗、特利鲁单抗、利匹鲁单抗、奈莫利尤单抗、抗 OX40 抗体、巴瑞替尼、阿布昔替尼和乌帕替尼的已发表的 II 期和 III 期数据。新型药物的引入可能会提供新的选择,但尚不清楚像单种白细胞介素抑制剂这样的窄作用药物在安全性和疗效方面将如何与 JAK 抑制剂等广泛作用药物进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ba5/7281689/54de1bc2fc3e/40265_2020_1335_Fig1_HTML.jpg

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