Why the study?
Conventional anti-platelet agents have limited efficacy in secondary stroke prevention under high shear stress with elevated VWF, prompting characterization of the anti-VWF aptamer BT200 in blood from patients with large artery atherosclerosis stroke.
Does BT200 inhibit VWF activity and platelet function in blood samples from patients with large artery atherosclerosis stroke?
Does BT200 inhibit VWF activity and platelet function in blood samples from patients with large artery atherosclerosis stroke?
The anti-VWF aptamer BT200 effectively inhibits VWF activity and platelet function in ex vivo blood samples from stroke patients, highlighting its potential as a novel antiplatelet agent for secondary stroke prevention.
Answers are grounded in this paper and cite their sources.
BT200 inhibits VWF activity in acute stroke blood; leaves open efficacy for secondary prevention in prospective trials.
The effect of conventional anti-platelet agents is limited in secondary stroke prevention, and their effects are blunted under high shear stress in the presence of increased levels of circulating von Willebrand factor (VWF). VWF is critically involved in thrombus formation at sites of stenotic extracranial/intracranial arteries. A third generation anti-VWF aptamer (BT200) has been generated which could be useful for secondary stroke prevention. To characterize the effects of BT200 in blood of patients with large artery atherosclerosis stroke (LAA). Blood samples were obtained from 33 patients with acute stroke or transient ischemic attack to measure inhibition of VWF activity and VWF-dependent platelet function. Patients who received clopidogrel or dual antiplatelet therapy did not differ in VWF dependent platelet function tests from aspirin treated patients. Of 18 patients receiving clopidogrel with or without aspirin, only 3 had a prolonged collagen adenosine diphosphate closure time, and none of the patients had ristocetin induced aggregation in the target range. BT200 concentration-dependently reduced median VWF activity from 178 to < 3%, ristocetin induced platelet aggregation from 40U to < 10U and prolonged collagen adenosine diphosphate closure times from 93 s to > 300 s. Baseline VWF activity correlated (r = 0.86, p < 0.001) with concentrations needed to reduce VWF activity to < 20% of normal, indicating that BT200 acts in a target concentration-dependent manner. Together with a long half-life supporting once weekly administration, the safety and tolerability observed in an ongoing phase I trial, and the existence of a reversal agent, BT200 is an interesting drug candidate.
No takes yet. Share an insight, caveat, or question.
Kovacevic et al. (2021) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: