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Updated: Sep 30, 2026

Ferric Chloride-induced Thrombosis Mouse Model on Carotid Artery and Mesentery Vessel
Published on: June 29, 2015
The thrombin mutant W215A/E217A shows safe and potent anticoagulant and antithrombotic effects in vivo
Andras Gruber1, Angelene M Cantwell, Enrico Di Cera
1Department of Biomedical Engineering and Yerkes Regional Primate Research Center, Emory University School of Medicine and Georgia Institute of Technology, Atlanta, Georgia 30322, USA.
Abstract:
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.

