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Serum cartilage oligomeric matrix protein (COMP) decreases in rheumatoid arthritis patients treated with infliximab or etanercept

机译:英夫利昔单抗或依那西普治疗的类风湿关节炎患者血清软骨寡聚基质蛋白(COMP)降低

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摘要

Changes in serum cartilage oligomeric matrix protein (COMP) were studied during a 6-month period from initiation of treatment of rheumatoid arthritis patients with either infliximab or etanercept, to elucidate whether the favourable results of tissue protection reported in clinical trials are corroborated by changing levels of circulating COMP. Rheumatoid arthritis patients commencing treatment with infliximab (N = 32) or etanercept (N = 17) were monitored in accordance with a structured protocol. Only patients who were not receiving glucocorticoids or who were on a stable dose of oral prednisolone (<10 mg daily) were included. Serum COMP was measured by a sandwich immunoassay based on two monoclonal antibodies against human COMP in samples obtained at treatment initiation and at 3 and 6 months. Serum COMP decreased at 3 months in both infliximab- and etanercept-treated patients (P < 0.001 and <0.005, respectively) and remained low at 6 months. There was no significant correlation between changes in or concentrations of serum COMP and serum C-reactive protein at any time point. A decrease in serum COMP was seen both in ACR20 responders (patients meeting the American College of Rheumatology criteria for 20% improvement) and in nonresponders. The pattern of changes of serum COMP, a marker for cartilage turnover, in these patient groups supports the interpretation that infliximab and etanercept have a joint protective effect. Serum COMP has potential as a useful marker for evaluating tissue effects of novel treatment modalities in rheumatoid arthritis.
机译:在开始用英夫利昔单抗或依那西普治疗类风湿性关节炎患者后的6个月内研究了血清软骨寡聚基质蛋白(COMP)的变化,以阐明是否通过改变水平来证实临床试验中报道的组织保护的有利结果循环COMP。根据结构化方案监测开始用英夫利昔单抗(N = 32)或依那西普(N = 17)治疗的类风湿关节炎患者。仅包括未接受糖皮质激素或稳定剂量口服泼尼松龙(每天<10 mg)的患者。通过三明治免疫测定法,基于在治疗开始时以及治疗3个月和6个月时获得的两种抗人COMP的单克隆抗体,对血清COMP进行测定。在英夫利昔单抗和依那西普治疗的患者中,血清COMP均在3个月时下降(分别为P <0.001和<0.005),并在6个月时保持较低水平。在任何时间点,血清COMP和血清C反应蛋白的变化或浓度之间均无显着相关性。在ACR20应答者(满足美国风湿病学会标准以改善20%的患者)和无应答者中,血清COMP均下降。在这些患者组中,血清COMP(软骨更新的标志物)的变化模式支持英夫利昔单抗和依那西普具有联合保护作用的解释。血清COMP有潜力作为评估类风湿关节炎新型治疗方式的组织效果的有用标志物。

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