Mugnier B, Bouvenot G
Service de rhumatologie, hôpital de la Conception, Marseille, France.
Rev Med Interne. 2000 Oct;21(10):854-62. doi: 10.1016/s0248-8663(00)00236-8.
Current slow-acting anti-rheumatic drugs available for rheumatoid arthritis can fail for certain severe cases; some are used empirically. Improvements in our knowledge of its pathogenesis and advances in molecular biology have made it possible to develop partially selective immunotherapy approaches.
Tumor necrosis factor-alpha (TNF-alpha) is a critical inflammatory mediator in rheumatoid arthritis and may therefore be a useful target for specific immunotherapy. This article summarizes clinical studies using anti-TNF-alpha antibodies. It appears that there is good evidence for both safety and beneficial effects of anti-TNF-alpha antibodies in short-term treatment of rheumatoid arthritis.
It remains to be determined whether specific blockade of a single inflammatory mediator may be useful in long-term management. Therapeutic strategies aimed at concomitantly interfering with multiple pathogenic pathways are currently under investigation.
目前用于类风湿性关节炎的慢作用抗风湿药物在某些严重病例中可能无效;有些是经验性使用。我们对其发病机制认识的提高以及分子生物学的进展使得开发部分选择性免疫治疗方法成为可能。
肿瘤坏死因子-α(TNF-α)是类风湿性关节炎中的一种关键炎症介质,因此可能是特异性免疫治疗的一个有用靶点。本文总结了使用抗TNF-α抗体的临床研究。似乎有充分证据表明抗TNF-α抗体在类风湿性关节炎的短期治疗中具有安全性和有益效果。
单一炎症介质的特异性阻断在长期治疗中是否有用仍有待确定。目前正在研究旨在同时干扰多种致病途径的治疗策略。