Sander O, Rau R
Rheumatologische Klinik, Evangelisches Fachkrankenhaus, Ratingen, Germany.
Int J Clin Pharmacol Ther. 1998 Nov;36(11):621-4.
Cytokines and T cells play a major role in the pathogenesis of rheumatoid arthritis (RA). Biologic targeting is a novel therapeutic approach. Published trials in humans are discussed in this paper.
CD4-positive T cells, proinflammatory cytokines like TNF-alpha, IL-1, IL-6 and gamma-IFN were major targets for therapy. Biologics were constructed of monoclonal human and non-human antibodies, chimerics of both, antiinflammatory regulatory proteins like IL-1 receptor antagonist, IL-10, and fusion proteins consisting of receptors and immunoglobulins.
More than 2000 humans with RA were exposed to biologics in the last decade. Both, toxic and safe, efficient and non-efficient drugs were tested. Phase II data could not confirm preliminary phase I data in several drugs tested. The pharmacokinetic profile of biologics is influenced by frequent induction of human anti drug antibodies.
The major role of cytokines in RA has been confirmed. Due to the limited long-term experience immunomodulation does not replace conventional pharmacotherapy.
细胞因子和T细胞在类风湿性关节炎(RA)的发病机制中起主要作用。生物靶向治疗是一种新型治疗方法。本文讨论了已发表的人体试验。
治疗的主要靶点是CD4阳性T细胞以及肿瘤坏死因子-α、白细胞介素-1、白细胞介素-6和γ-干扰素等促炎细胞因子。生物制剂由单克隆人源和非人源抗体、两者的嵌合体、白细胞介素-1受体拮抗剂、白细胞介素-10等抗炎调节蛋白以及由受体和免疫球蛋白组成的融合蛋白构建而成。
在过去十年中,超过2000名类风湿性关节炎患者接受了生物制剂治疗。对毒性和安全性、有效性和无效性的药物都进行了测试。在几种受试药物中,II期数据未能证实I期初步数据。生物制剂的药代动力学特征受人体抗药物抗体频繁诱导的影响。
细胞因子在类风湿性关节炎中的主要作用已得到证实。由于长期经验有限,免疫调节不能替代传统药物治疗。