Harrington Robert, Al Nokhatha Shamma Ahmad, Conway Richard
Department of Rheumatology, St. James's Hospital, Dublin, Ireland.
Biologics. 2021 Jan 6;15:17-29. doi: 10.2147/BTT.S229662. eCollection 2021.
Glucocorticoids have been the mainstay of treatment in giant cell arteritis (GCA) for the past 70 years. Conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) have largely failed to show significant clinical efficacy or reduction of the glucocorticoid burden in GCA. Tocilizumab is the first biologic to make a substantial impact in GCA treatment. With the current understanding of GCA pathogenesis implicating multiple cytokines, notably interleukin (IL) 6, IL-12, IL-23, IL-1β, and the role of janus kinases (JAKs) and the signal transducer and activator of transcription (STAT) pathway in these cytokines, many biologics are currently being investigated in GCA. This review article looks at the existing evidence for biologic agents in GCA. In addition to tocilizumab, the potential role of ustekinumab, abatacept, JAK inhibitors and other promising biologics in GCA are discussed in detail. A treatment algorithm based on the best evidence to date is also presented.
在过去70年里,糖皮质激素一直是巨细胞动脉炎(GCA)治疗的主要手段。传统的合成改善病情抗风湿药(csDMARDs)在GCA中大多未能显示出显著的临床疗效,也未能减轻糖皮质激素负担。托珠单抗是首个在GCA治疗中产生重大影响的生物制剂。鉴于目前对GCA发病机制的认识涉及多种细胞因子,尤其是白细胞介素(IL)-6、IL-12、IL-23、IL-1β,以及janus激酶(JAKs)和信号转导及转录激活因子(STAT)途径在这些细胞因子中的作用,目前许多生物制剂正在GCA中进行研究。这篇综述文章探讨了GCA中生物制剂的现有证据。除托珠单抗外,还详细讨论了优特克单抗、阿巴西普、JAK抑制剂和其他有前景的生物制剂在GCA中的潜在作用。还提出了基于迄今最佳证据的治疗方案。