Lubrano Ennio, Perrotta Fabio Massimo
a Dipartimento di Medicina e Scienze della Salute "Vincenzo Tiberio" , Università degli Studi del Molise , Campobasso , Italy.
Expert Rev Clin Immunol. 2017 Aug;13(8):815-821. doi: 10.1080/1744666X.2017.1327354. Epub 2017 May 16.
Psoriatic arthritis (PsA) is a chronic inflammatory articular disease characterized by psoriasis, synovitis and enthesitis. Current treatment of PsA is mainly based on the use of classical and biological DMARDs; however, 30-40% of patients could not respond to these or have a loss of response. Areas covered: Recently, the discovery of new pathogenic mechanisms have made possible the development of new drugs that target the IL-17 with the possibility to interfere with the Th17 cells that are considered the cell type mainly involved in the development of the inflammation in PsA. New molecules have shown efficacy and safety over the various components of the disease in randomized clinical trials. These drugs have been recently approved for the treatment of PsA and included in the newest treatment recommendations. Other molecules are currently being tested in phase III clinical trials and are potential new treatment options for PsA. Expert Commentary: The aim of this paper is to review the role of IL-17 in the pathogenesis and treatment of PsA, with a discussion on the emerging anti-IL-17 drugs for PsA.
银屑病关节炎(PsA)是一种慢性炎症性关节疾病,其特征为银屑病、滑膜炎和附着点炎。PsA的当前治疗主要基于使用传统和生物性改善病情抗风湿药(DMARDs);然而,30%-40%的患者对这些药物无反应或出现反应丧失。涵盖领域:最近,新致病机制的发现使得开发靶向IL-17的新药成为可能,这些新药有可能干扰Th17细胞,Th17细胞被认为是主要参与PsA炎症发生的细胞类型。新分子在随机临床试验中已显示出对该疾病各个组成部分的疗效和安全性。这些药物最近已被批准用于治疗PsA,并被纳入最新的治疗推荐中。其他分子目前正在进行III期临床试验,是PsA潜在的新治疗选择。专家评论:本文旨在综述IL-17在PsA发病机制和治疗中的作用,并讨论新兴的用于治疗PsA的抗IL-17药物。