Buch Maya H, Vital Edward M, Emery Paul
Academic Unit of Musculoskeletal Disease, University of Leeds, Chapeltown Road, Leeds, LS7 4SA, UK.
Arthritis Res Ther. 2008;10 Suppl 1(Suppl 1):S5. doi: 10.1186/ar2416. Epub 2008 Oct 15.
T-cell biology has regained importance in the pathogenesis of rheumatoid arthritis. Despite the significant improvements associated with the introduction of tumor necrosis factor-alpha blockade, reasonable proportions of failures and suboptimal responses have been reported, necessitating a search for alternative targeted therapies. This has included drug therapy designed to interrupt T-cell activation via the co-stimulation pathway. Abatacept is a recombinant fusion protein that blocks the co-stimulatory signal mediated by the CD28-CD80/86 pathway, which is required for T-cell activation. Several clinical trials have confirmed the safety and efficacy of this drug in the treatment of rheumatoid arthritis. This review summarizes the clinical data supporting this line of treatment and considers the safety and efficacy data from phase II and III trials.
T细胞生物学在类风湿性关节炎的发病机制中再度变得重要。尽管随着肿瘤坏死因子-α阻断剂的引入取得了显著进展,但仍有相当比例的治疗失败和反应欠佳的情况被报道,因此有必要寻找替代的靶向治疗方法。这包括旨在通过共刺激途径中断T细胞活化的药物治疗。阿巴西普是一种重组融合蛋白,可阻断由CD28-CD80/86途径介导的共刺激信号,而该信号是T细胞活化所必需的。多项临床试验已证实该药物治疗类风湿性关节炎的安全性和有效性。本综述总结了支持这一治疗方法的临床数据,并考量了II期和III期试验的安全性和有效性数据。