Gruber Andras, Cantwell Angelene M, Di Cera Enrico, Hanson Stephen R
Department of Biomedical Engineering and Yerkes Regional Primate Research Center, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, Georgia 30322, USA.
J Biol Chem. 2002 Aug 2;277(31):27581-4. doi: 10.1074/jbc.C200237200. Epub 2002 Jun 17.
Administration of the thrombin mutant W215A/E217A (WE), rationally designed for selective activation of the anticoagulant protein C, elicits safe and potent anticoagulant and antithrombotic effects in a baboon model of platelet-dependent thrombosis. The lowest dose of WE tested (0.011 mg/kg bolus) reduced platelet thrombus accumulation by 80% and was at least as effective as the direct administration of 40-fold more (0.45 mg/kg bolus) activated protein C. WE-treated animals showed no detectable hemorrhage or organ failure. No procoagulant activity could be detected for up to 1 week in baboon plasma obtained following WE administration. These results show that engineered thrombin derivatives that selectively activate protein C may represent useful therapeutic agents for the treatment of thrombotic disorders.
凝血酶突变体W215A/E217A(WE)是为选择性激活抗凝蛋白C而合理设计的,在依赖血小板的血栓形成狒狒模型中,它能引发安全且强效的抗凝和抗血栓作用。所测试的最低剂量的WE(0.011mg/kg推注)使血小板血栓积聚减少了80%,其效果至少与直接给予剂量高40倍(0.45mg/kg推注)的活化蛋白C相同。接受WE治疗的动物未出现可检测到的出血或器官衰竭。在给予WE后采集的狒狒血浆中,长达1周都检测不到促凝活性。这些结果表明,选择性激活蛋白C的工程化凝血酶衍生物可能是治疗血栓性疾病的有用治疗剂。