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Updated: Jul 4, 2025

Ferric Chloride-induced Thrombosis Mouse Model on Carotid Artery and Mesentery Vessel
Published on: June 29, 2015
Pharmacologic targeting of coagulation factors XII and XI by monoclonal antibodies reduces thrombosis in nitinol
Novella M Keeling1, Michael Wallisch2, Jennifer Johnson3
1Department of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA; Biomedical Engineering Program, University of Colorado Boulder, Boulder, Colorado, USA.
New therapies targeting coagulation factors (F)XI and FXII show promise for preventing thrombosis associated with cardiovascular devices. FXI inhibition proved most effective in reducing device-related blood clots, offering a safer alternative to current treatments.
Area of Science:
- Biomedical Engineering
- Hematology
- Cardiovascular Research
Background:
- Cardiovascular implantable devices, like vascular stents, are vital for treating heart disease.
- Current antithrombotic therapies carry significant bleeding risks.
- Coagulation factors XI and XII are potential targets for safer antithrombotic strategies.
Purpose of the Study:
- To evaluate the efficacy of monoclonal antibodies targeting coagulation factors (F)XI and FXII.
- To assess their role in preventing thrombosis related to vascular devices.
Main Methods:
- Utilized a nonhuman primate model to study nitinol stent-related thrombosis.
- Examined the effects of function-blocking monoclonal antibodies against FXI and FXII.
- Tested under both arterial and venous flow conditions.
Main Results:
- Both FXI and FXII inhibition reduced markers of stent-induced thrombosis in vitro and ex vivo.
- FXI inhibition demonstrated superior effectiveness in mitigating thrombosis across varied flow conditions.
Conclusions:
- Inhibitors of the coagulation contact pathway show potential for clinical use with cardiovascular devices.
- Further research supports the translation of these findings for improved patient outcomes.
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