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Prophylactic and therapeutic effects of a humanized monoclonal antibody against the IL-2 receptor (DACLIZUMAB) on collagen-induced arthritis (CIA) in rhesus monkeys

机译:抗IL-2受体的人源化单克隆抗体(DACLIZUMAB)对恒河猴胶原诱导的关节炎(CIA)的预防和治疗作用

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摘要

CIA in the rhesus monkey is an autoimmune-based polyarthritis with inflammation and erosion of synovial joints that shares various features with human rheumatoid arthritis (RA). The close phylogenetic relationship between man and rhesus monkey makes the model very suitable for preclinical safety and efficacy testing of new therapeutics with exclusive reactivity in primates. In this study we have investigated the prophylactic and therapeutic effects of a humanized monoclonal antibody (Daclizumab) against the α-chain of the IL-2 receptor (CD25). When Daclizumab treatment was started well after immunization but before the expected onset of CIA a significant reduction of joint-inflammation and joint-erosion was observed. A therapeutic treatment, initiated as soon as the first clinical signs of CIA were observed, proved also effective since joint-degradation was abrogated. The results of this study indicate that Daclizumab has clinical potential for the treatment of RA during periods of active inflammation and suppression of the destruction of the joint tissues.
机译:恒河猴中的CIA是一种基于自身免疫的多关节炎,具有炎症和滑膜关节侵蚀,与人类类风湿关节炎(RA)具有多种特征。人与恒河猴之间的亲密系统发育关系使该模型非常适合灵长类中具有独家反应性的新疗法的临床前安全性和功效测试。在这项研究中,我们研究了针对IL-2受体(CD25)α链的人源化单克隆抗体(Daclizumab)的预防和治疗作用。当达克珠单抗治疗在免疫后开始但在预期的CIA发作之前开始时,观察到关节炎症和关节侵蚀明显减少。观察到CIA的首次临床体征后立即开始的治疗方法也被证明是有效的,因为消除了关节退化。这项研究的结果表明,达克珠单抗在活动性炎症和抑制关节组织破坏期间具有治疗RA的临床潜力。

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