Taylor P C
The Kennedy Institute Division, Imperial College School of Medicine, London, UK.
Curr Opin Rheumatol. 2001 May;13(3):164-9. doi: 10.1097/00002281-200105000-00003.
Recently published studies confirm that the long-term use of biologicals targeting tumor necrosis factor-alpha (TNF-alpha) in therapy for rheumatoid arthritis (RA) gives rise to sustained improvement in symptoms and signs of disease provided the anti-TNF agent is efficacious and of low immunogenicity. The current regimens for infliximab 3 or 10 mg/kg infusion in combination with weekly oral methotrexate, or of etanercept 25 mg subcutaneously twice per week, appear to fulfill these criteria. D2E7, a "human" antibody produced by phage display, has also been used for over a year. It has recently emerged that anti-TNF therapy protects joints from structural damage. The 1-year data for infliximab and methotrexate combination therapy suggest that this regimen reduces disability. In early RA, etanercept acts more rapidly than methotrexate to decrease symptoms and retard the progression of erosions. In conclusion, for patients with established and early RA, anti-TNF therapies set a new standard for symptom control and joint protection.
最近发表的研究证实,在类风湿关节炎(RA)治疗中,长期使用靶向肿瘤坏死因子-α(TNF-α)的生物制剂,只要抗TNF药物有效且免疫原性低,就能使疾病的症状和体征得到持续改善。目前英夫利昔单抗3或10mg/kg静脉输注联合每周口服甲氨蝶呤,或依那西普25mg皮下注射每周两次的治疗方案似乎符合这些标准。D2E7,一种通过噬菌体展示产生的“人”抗体,也已使用一年多。最近发现抗TNF治疗可保护关节免受结构损伤。英夫利昔单抗与甲氨蝶呤联合治疗的1年数据表明,该方案可减少残疾。在早期RA中,依那西普比甲氨蝶呤起效更快,可减轻症状并延缓侵蚀进展。总之,对于已确诊的RA患者和早期RA患者,抗TNF治疗为症状控制和关节保护树立了新的标准。