Maini R N, Taylor P C
Kennedy Institute of Rheumatology, London, UK.
Annu Rev Med. 2000;51:207-29. doi: 10.1146/annurev.med.51.1.207.
Tumor necrosis factor alpha (TNF alpha) and interleukin-1 (IL-1) are important in mediating inflammation in rheumatoid arthritis (RA). Randomized phase II and III clinical trials of anti-TNF reagents (infliximab and etanercept) have demonstrated an acceptable safety profile and marked clinical efficacy in cases of RA that have not responded adequately to conventional therapy. Combination therapy with methotrexate (MTX) appears to be particularly effective in patients whose disease activity persists despite prior disease-modifying antirheumatic drugs (DMARDs) and ongoing MTX monotherapy. DMARD-recalcitrant disease may become the main indication for the use of anti-TNF drugs in patients with RA. Trials of IL-1 receptor antagonist show a relatively modest anti-inflammatory effect and a possible retardation of joint damage. Whether anti-TNF therapy protects joints from structural damage is under investigation. One anti-TNF reagent has already been approved in the United States for the treatment of RA, and other cytokine antagonists or agonists are under development.
肿瘤坏死因子α(TNFα)和白细胞介素-1(IL-1)在类风湿关节炎(RA)的炎症介导过程中起重要作用。抗TNF试剂(英夫利昔单抗和依那西普)的随机II期和III期临床试验已证明,在对传统治疗反应不佳的RA病例中,其安全性可接受且临床疗效显著。对于那些尽管先前使用过改善病情抗风湿药(DMARDs)且正在进行甲氨蝶呤(MTX)单药治疗但疾病活动仍持续的患者,MTX联合治疗似乎特别有效。DMARD难治性疾病可能成为RA患者使用抗TNF药物的主要适应症。IL-1受体拮抗剂的试验显示出相对适度的抗炎作用以及可能延缓关节损伤。抗TNF治疗是否能保护关节免受结构损伤正在研究中。一种抗TNF试剂已在美国获批用于治疗RA,其他细胞因子拮抗剂或激动剂正在研发中。