Atzeni Fabiola, Carriero Antonio, Boccassini Laura, D'Angelo Salvatore
Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Rheumatology Institute of Lucania (IReL), Rheumatology Department of Lucania, San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.
Immunotargets Ther. 2021 May 3;10:141-153. doi: 10.2147/ITT.S259126. eCollection 2021.
Axial spondyloarthritis (axSpA) describes a group of chronic inflammatory rheumatic diseases primarily involving the axial skeleton. IL-17 is involved in the pathogenesis of numerous inflammatory diseases, including inflammatory arthritis. Until a few years ago, the only biological agents licensed for the treatment of axSpA and nr-axSpA were TNF inhibitors. However, as some patients did not respond to TNF inhibition or experienced secondary failure, the introduction of the first two IL-17 inhibitors (secukinumab [SEC] and ixekizumab [IXE]) has extended the treatment options, and there are now three others (bimekizumab, brodalumab and netakimab) in various stages of clinical development. The last ten years have seen the development of a number of therapeutic recommendations that aimed at improving the management of axSpA patients. The aim of this narrative review of the published literature concerning the role of IL-17 in the pathogenesis of SpA, and the role of IL-17 inhibitors in the treatment of axSpA, is to provide a comprehensive picture of the clinical efficacy and safety of the drugs themselves, and the treatment strategies recommended in the international guidelines.
轴性脊柱关节炎(axSpA)是一组主要累及中轴骨骼的慢性炎症性风湿性疾病。白细胞介素-17(IL-17)参与包括炎性关节炎在内的多种炎性疾病的发病机制。直到几年前,唯一获批用于治疗axSpA和非放射学中轴性脊柱关节炎(nr-axSpA)的生物制剂还是肿瘤坏死因子(TNF)抑制剂。然而,由于一些患者对TNF抑制治疗无反应或出现继发性失效,首批两种IL-17抑制剂(司库奇尤单抗[SEC]和依奇珠单抗[IXE])的引入扩展了治疗选择,目前还有其他三种药物(比美吉珠单抗、布罗达单抗和奈他珠单抗)正处于不同阶段的临床开发中。在过去十年中,出现了一些旨在改善axSpA患者管理的治疗建议。这篇关于已发表文献的叙述性综述旨在探讨IL-17在脊柱关节炎发病机制中的作用,以及IL-17抑制剂在axSpA治疗中的作用,以全面呈现这些药物本身的临床疗效和安全性,以及国际指南中推荐的治疗策略。