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探索治疗领域:关于皮肤科局部和口服磷酸二酯酶-4抑制剂的叙述性综述

Exploring the Therapeutic Landscape: A Narrative Review on Topical and Oral Phosphodiesterase-4 Inhibitors in Dermatology.

作者信息

Carmona-Rocha Elena, Rusiñol Lluís, Puig Lluís

机构信息

Department of Dermatology, Hospital de la Santa Creu i Sant Pau, 08041 Barcelona, Spain.

Institut de Recerca Sant Pau (IR SANT PAU), 08041 Barcelona, Spain.

出版信息

Pharmaceutics. 2025 Jan 12;17(1):91. doi: 10.3390/pharmaceutics17010091.

Abstract

Phosphodiesterase-4 (PDE4) is involved in the synthesis of inflammatory cytokines that mediate several chronic inflammatory disorders, including psoriasis and atopic dermatitis. In recent years, the therapeutic armamentarium in dermatology has expanded with the introduction of PDE4 inhibitors, both in oral and topical formulations. PDE4 inhibitors have gained increasing interest due to their remarkable safety record and ease of prescription, as evidenced by the recent influx of literature detailing its off-label uses. Apremilast was the first PDE4 inhibitor approved by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for psoriasis, psoriatic arthritis, and oral ulcers of Behcet's disease. Off-label use has been reported in diverse dermatological conditions, including aphthous stomatitis, chronic actinic dermatitis, atopic dermatitis, cutaneous sarcoidosis, hidradenitis suppurativa, lichen planus, and discoid lupus erythematosus. Roflumilast is a PDE4 inhibitor that was approved by the FDA and the EMA as an oral treatment of chronic obstructive pulmonary disease. Since patent expiration, several generic formulations of oral roflumilast have become available, and various studies have documented its off-label use in psoriasis and other dermatological conditions such as hidradenitis suppurativa, recurrent oral aphthosis, nummular eczema, lichen planus, and Behçet's disease. Topical roflumilast has received FDA approval for treatment of plaque psoriasis and seborrheic dermatitis. The favorable safety profile encourages its long-term use as an alternative to corticosteroids, addressing the chronic nature of many dermatological conditions. New oral PDE4 inhibitors are being developed, such as orismilast (LEO-32731), mufemilast (Hemay005), difamilast (OPA-15406) or lotamilast (E6005/RVT-501), among others. This narrative review provides a comprehensive synthesis of the pharmacology, clinical efficacy, safety profile, and practical considerations regarding the oral and topical use of PDE4 inhibitors in dermatology.

摘要

磷酸二酯酶-4(PDE4)参与介导多种慢性炎症性疾病(包括银屑病和特应性皮炎)的炎性细胞因子的合成。近年来,随着口服和外用剂型的PDE4抑制剂的引入,皮肤科的治疗手段有所扩展。PDE4抑制剂因其出色的安全记录和易于处方而受到越来越多的关注,最近大量详细描述其非标签用途的文献涌入就证明了这一点。阿普斯特是首个被美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准用于治疗银屑病、银屑病关节炎和白塞病口腔溃疡的PDE4抑制剂。在多种皮肤病中都有其非标签使用的报道,包括复发性口腔溃疡、慢性光化性皮炎、特应性皮炎、皮肤结节病、化脓性汗腺炎、扁平苔藓和盘状红斑狼疮。罗氟司特是一种PDE4抑制剂,被FDA和EMA批准用于口服治疗慢性阻塞性肺疾病。自专利到期以来,已有几种口服罗氟司特的仿制药上市,各种研究记录了其在银屑病和其他皮肤病(如化脓性汗腺炎、复发性口腔溃疡、钱币状湿疹、扁平苔藓和白塞病)中的非标签使用情况。外用罗氟司特已获得FDA批准用于治疗斑块状银屑病和脂溢性皮炎。其良好的安全性促使它可长期用作皮质类固醇的替代品,以应对许多皮肤病的慢性特性。新型口服PDE4抑制剂正在研发中,如奥瑞司特(LEO-32731)、穆非司特(Hemay005)、地法司特(OPA-15406)或洛他司特(E6005/RVT-501)等。本叙述性综述全面综合了PDE4抑制剂在皮肤科口服和外用方面的药理学、临床疗效、安全性概况及实际考量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/290e/11769339/b590eded7cc4/pharmaceutics-17-00091-g001.jpg

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