Smolen Josef S, Aletaha Daniel, Koeller Marcus, Weisman Michael H, Emery Paul
Division of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Lancet. 2007 Dec 1;370(9602):1861-74. doi: 10.1016/S0140-6736(07)60784-3.
Rheumatoid arthritis is characterised by pain, swelling, and destruction of joints, with resultant disability. Only disease-modifying antirheumatic drugs can interfere with the disease process. In the past few years, biological agents, especially inhibitors of tumour necrosis factor, have allowed for hitherto unseen therapeutic benefit, although even with these drugs the frequency and degree of responses are restricted. Therefore, new agents are needed, and three novel biological compounds for treatment of rheumatoid arthritis have already been used in practice or are on the horizon: rituximab (anti-CD20), abatacept (cytotoxic T-lymphocyte antigen 4 immunoglobulin), and tocilizumab (anti-interleukin 6 receptor). We discuss the targets of these drugs, the roles of these targets in the pathogenesis of rheumatoid arthritis, and the efficacy and adverse effects of these agents from clinical trial data. Novel therapeutic strategies in conjunction with optimised disease assessment for better treatment of rheumatoid arthritis and an outlook into potential future targets are also presented.
类风湿性关节炎的特点是关节疼痛、肿胀和破坏,并导致残疾。只有改善病情的抗风湿药物才能干扰疾病进程。在过去几年中,生物制剂,尤其是肿瘤坏死因子抑制剂,带来了前所未有的治疗益处,尽管即便使用这些药物,反应的频率和程度也受到限制。因此,需要新的药物,三种用于治疗类风湿性关节炎的新型生物化合物已在实际中使用或即将出现:利妥昔单抗(抗CD20)、阿巴西普(细胞毒性T淋巴细胞抗原4免疫球蛋白)和托珠单抗(抗白细胞介素6受体)。我们根据临床试验数据讨论这些药物的靶点、这些靶点在类风湿性关节炎发病机制中的作用以及这些药物的疗效和不良反应。还介绍了结合优化疾病评估以更好治疗类风湿性关节炎的新型治疗策略以及对潜在未来靶点的展望。