Serio I, Tovoli F
Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Drugs Today (Barc). 2018 Mar;54(3):219-230. doi: 10.1358/dot.2018.54.3.2788019.
Rheumatoid arthritis (RA) is an immune-mediated condition which primarily affects the joints, but with critical extra-articular manifestations, including a significantly increased cardiovascular risk. Patients suffering from RA can develop deforming and disabling alterations of the affected joints. Their quality of life can be substantially affected, and their life expectancy is shorter compared to that of healthy subjects. Fortunately, several pathogenic mechanisms characterizing RA have been identified, leading to the development of targeted drugs. Inhibitors of tumor necrosis factor (TNF) were the first developed among biological medications and they dramatically changed the therapeutic perspectives of RA patients. Now, 20 years after the licensing of etanercept (the first anti-TNF drug), more than 10 different biological agents have been approved by the U.S. Food and Drug Administration (FDA). Additionally, more and more drugs are under investigation in clinical trials. This review will focus on the more recently approved monoclonal antibodies and the more promising antibodies under investigation.
类风湿关节炎(RA)是一种免疫介导性疾病,主要影响关节,但伴有严重的关节外表现,包括心血管风险显著增加。患有RA的患者会出现受累关节的变形和致残性改变。他们的生活质量会受到严重影响,与健康受试者相比,预期寿命较短。幸运的是,已经确定了几种表征RA的致病机制,从而促成了靶向药物的研发。肿瘤坏死因子(TNF)抑制剂是最早研发的生物药物,它们极大地改变了RA患者的治疗前景。现在,在依那西普(第一种抗TNF药物)获批20年后,美国食品药品监督管理局(FDA)已批准了10多种不同的生物制剂。此外,越来越多的药物正在临床试验中进行研究。本综述将聚焦于最近获批的单克隆抗体以及正在研究的更有前景的抗体。