Chimenti Maria Sole, Conigliaro Paola, Biancone Livia, Perricone Roberto
Rheumatology, Allergology and Immunology, University of Rome Tor Vergata, Via Montpellier 1, Rome, Lazio, Italy.
Rheumatology, Allergology and Clinical Immunology, Department of Systems Medicine, University of Rome Tor Vergata, Rome, Lazio, Italy.
Ther Adv Musculoskelet Dis. 2021 Feb 18;13:1759720X20977777. doi: 10.1177/1759720X20977777. eCollection 2021.
Psoriatic arthritis (PsA) and ulcerative colitis (UC) are immune-mediated diseases that cause significant burden worldwide. Recent advances in their management have improved patient outcomes. However, significant unmet needs still remain as not all patients respond to current treatments, and patients may lose responsiveness over time. An improved understanding of the pathophysiology of these diseases has brought about the development of novel disease-modifying agents, including interleukin inhibitors and, more recently, Janus kinase (JAK) inhibitors. With the approval of tofacitinib for the treatment of adults with active PsA and in adult patients with moderately-to-severely active UC, JAK inhibitors have recently entered the treatment armamentarium for PsA and UC. A number of other JAK inhibitors are also undergoing clinical development and are currently in phase III trials. This review provides an overview of the current therapeutic options for PsA and UC, with a focus on the JAK inhibitors.
银屑病关节炎(PsA)和溃疡性结肠炎(UC)是免疫介导的疾病,在全球范围内造成了重大负担。它们治疗方面的最新进展改善了患者的治疗效果。然而,由于并非所有患者都对当前治疗有反应,且患者可能会随着时间推移失去反应性,因此仍存在重大未满足需求。对这些疾病病理生理学的进一步了解推动了新型病情改善药物的研发,包括白细胞介素抑制剂,以及最近的 Janus 激酶(JAK)抑制剂。随着托法替布被批准用于治疗活动性 PsA 的成人患者以及中度至重度活动性 UC 的成人患者,JAK 抑制剂最近已进入 PsA 和 UC 的治疗药物库。其他一些 JAK 抑制剂也正在进行临床开发,目前处于 III 期试验阶段。本综述概述了 PsA 和 UC 当前的治疗选择,重点关注 JAK 抑制剂。