首页> 美国卫生研究院文献>TH Open: Companion Journal to Thrombosis and Haemostasis >Emicizumab A Bispecific Antibody to Factors IX/IXa and X/Xa Does Not Interfere with Antithrombin or TFPI Activity In Vitro
【2h】

Emicizumab A Bispecific Antibody to Factors IX/IXa and X/Xa Does Not Interfere with Antithrombin or TFPI Activity In Vitro

机译:Emicizumab是一种针对因子IX / IXa和X / Xa的双特异性抗体在体外不会干扰抗凝血酶或TFPI的活性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Emicizumab is a humanized bispecific antibody that binds simultaneously to factor (F) IXa and FX replacing the cofactor function of FVIIIa. Because emicizumab recognizes FIX/FIXa and FX/FXa, a question may arise whether emicizumab competes with antithrombin (AT) and/or tissue factor pathway inhibitor (TFPI), thereby enhancing overall hemostatic potential by blocking their antihemostatic effects. To address this question, we performed enzymatic assays using purified coagulation factors to confirm whether emicizumab interferes with the action of AT on FIXa or FXa, or with the action of TFPI on FXa. In those assays, we found no interference of emicizumab on the actions of AT and TFPI. We next assessed emicizumab's influences on the anticoagulation actions of AT or TFPI in thrombin generation assays triggered with FXIa or tissue factor (TF) in AT-depleted or TFPI-depleted plasma supplemented with AT or TFPI in vitro. In those assays, we employed anti-FIXa and anti-FX monospecific one-armed antibodies derived from emicizumab instead of emicizumab itself so as to prevent emicizumab's FVIIIa cofactor activity from boosting thrombin generation. Consequently, we found that neither anti-FIXa, anti-FX monospecific antibody, nor the mixture of the two interfered with the anticoagulation actions of AT or TFPI in plasma. Although emicizumab can bind to FIXa and FXa, our results showed no interference of emicizumab with the action of AT or TFPI on FIXa or FXa. This indicates that the presence of emicizumab is irrelevant to the action of AT and TFPI, and thus should not alter the coagulant/anticoagulant balance related to AT and TFPI.
机译:Emicizumab是一种人源化双特异性抗体,可同时与因子(F)IXa和FX结合,取代FVIIIa的辅因子功能。由于艾米单抗可识别FIX / FIXa和FX / FXa,因此可能会产生一个问题,即艾米单抗是否与抗凝血酶(AT)和/或组织因子途径抑制剂(TFPI)竞争,从而通过阻断其止血作用来增强总体止血潜力。为了解决这个问题,我们使用纯化的凝血因子进行了酶促测定,以确认艾米单抗是否干扰AT对FIXa或FXa的作用,或TFPI对FXa的作用。在那些测定中,我们发现艾米珠单抗对AT和TFPI的作用没有干扰。接下来,我们在体外补充了AT或TFPI的AT耗尽或TFPI耗尽的血浆中,用FXIa或组织因子(TF)触发的凝血酶生成测定中,评估了emicizumab对AT或TFPI的抗凝作用的影响。在那些测定中,我们采用了源自艾米单抗的抗FIXa和抗FX单特异性单臂抗体,而不是艾米单抗本身,以防止艾米单抗的FVIIIa辅因子活性促进凝血酶的产生。因此,我们发现抗FIXa,抗FX单特异性抗体或两者的混合物均不会干扰血浆中AT或TFPI的抗凝作用。尽管艾米单抗可以与FIXa和FXa结合,但我们的结果表明,艾米单抗在FIXa或FXa上不受AT或TFPI的干扰。这表明艾米珠单抗的存在与AT和TFPI的作用无关,因此不应改变与AT和TFPI有关的凝血/抗凝平衡。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号