Moreland L W
Arthritis Clinical Intervention Program, Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Rheum Dis Clin North Am. 2001 May;27(2):445-91. doi: 10.1016/s0889-857x(05)70212-x.
The encouraging clinical results observed in trials using anti-TNF therapy clearly warrant further studies to determine whether TNF inhibitors are capable of modifying the destructive component of this disease in long-term follow-up studies as well as to assess the safety of long-term use (see the article by Keystone in this issue). It is also reasonable to propose that interfering with the cytokine cascade earlier in the course of disease may be of even greater therapeutic benefit. As the pathogenetic mechanisms in RA are more clearly defined, especially in early disease and in those individuals destined to develop severe disease, the potential of other biologic agents to specifically inhibit these critical pathways may provide better treatments for our patients. Many potential targets in the immune-mediated process of RA are currently being rigorously evaluated in clinical trials. Use of combinations of biologic therapies, perhaps in human patients with RA, should be of considerable interest in future trials.
在使用抗TNF治疗的试验中观察到的令人鼓舞的临床结果,显然有必要进行进一步研究,以确定TNF抑制剂在长期随访研究中是否能够改变该疾病的破坏成分,并评估长期使用的安全性(见本期Keystone的文章)。也有理由提出,在疾病进程中更早地干扰细胞因子级联反应可能具有更大的治疗益处。随着类风湿关节炎发病机制的更明确界定,特别是在早期疾病以及那些注定会发展为严重疾病的个体中,其他生物制剂特异性抑制这些关键途径的潜力可能为我们的患者提供更好的治疗方法。目前许多类风湿关节炎免疫介导过程中的潜在靶点正在临床试验中进行严格评估。生物疗法联合使用,或许在类风湿关节炎患者中应用,在未来试验中应会备受关注。