Abstract

ObjectivesWe examined the effect of Revacept, an Fc fusion protein which is specifically linked to the extracellular domain of glycoprotein VI (GPVI), on thrombus formation after vessel wall injury and on experimental stroke in mice.BackgroundSeveral antiplatelet drugs for the treatment of myocardial infarction or ischemic stroke with potent anti-ischemic effects have been developed, but all incur a significant risk of bleeding.MethodsPlatelet adhesion and thrombus formation after endothelial injury was monitored in the carotid artery by intra-vital fluorescence microscopy. The morphological and clinical consequences of stroke were investigated in a mouse model with a one hour-occlusion of the middle cerebral artery.ResultsThrombus formation was significantly decreased after endothelial injury by 1 mg/kg Revacept IV, compared to Fc only. 1 mg/kg Revacept IV applied in mice with ischemic stroke immediately before reperfusion significantly improved functional outcome, cerebral infarct size and edema compared to Fc only. Also treatment with 10 mg/kg rtPA was effective, and functional outcome was similar in both treatment groups. The combination of Revacept with rtPA leads to increased reperfusion compared to treatment with either agent alone. In contrast to rtPA, however, there were no signs of increased intracranial bleeding with Revacept. Both rtPA and Revacept improved survival after stroke compared to placebo treatment. Revacept and vWF bind to collagen and Revacept competitively prevented the binding of vWF to collagen.ConclusionsRevacept reduces arterial thrombus formation, reduces cerebral infarct size and edema after ischemic stroke, improves functional and prognostic outcome without intracranial bleeding. Revacept not only prevents GPVI-mediated, but probably also vWF-mediated platelet adhesion and aggregate formation. Therefore Revacept might be a potent and safe tool to treat ischemic complications of stroke.

Highlights

  • Ischemic stroke is the most frequent disabling disease and a leading cause of death above the age of 60 years [1]

  • Thrombus formation was significantly decreased after endothelial injury by 1 mg/kg Revacept IV, compared to Fc only. 1 mg/kg Revacept IV applied in mice with ischemic stroke immediately before reperfusion significantly improved functional outcome, cerebral infarct size and edema compared to Fc only

  • The combination of Revacept with recombinant tissue plasminogen activator (rtPA) leads to increased reperfusion compared to treatment with either agent alone

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Summary

Introduction

Ischemic stroke is the most frequent disabling disease and a leading cause of death above the age of 60 years [1]. GPVI is the major signalling receptor for collagen and exclusively expressed on platelets and megakaryocytes initiating platelet recruitment at sites of vascular injury [6,7] Both blocking of GPIba and GPVI with specific antibodies led to a reduced infarct volume and a significantly improved functional outcome in an acute stroke model in mice with one hour occlusion of the middle cerebral artery (MCA) [8]. This finding was confirmed in vWF-/mice [9]. Several antiplatelet drugs for the treatment of myocardial infarction or ischemic stroke with potent antiischemic effects have been developed, but all incur a significant risk of bleeding

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