Preclinical Development of a vWF Aptamer to Limit Thrombosis and Engender Arterial Recanalization of Occluded Vessels.

Journal Article (Journal Article)

Endothelial surface and circulating glycoprotein von Willebrand factor (vWF) regulates platelet adhesion and is associated with thrombotic diseases, including ischemic stroke, myocardial infarction, and peripheral vascular disease. Thrombosis, as manifested in these diseases, is the leading cause of disability and death in the western world. Current parenteral antithrombotic and thrombolytic agents used to treat these conditions are limited by a short therapeutic window, irreversibility, and major risk of hemorrhage. To overcome these limitations, we developed a novel anti-vWF aptamer, called DTRI-031, that selectively binds and inhibits vWF-mediated platelet adhesion and arterial thrombosis while enabling rapid reversal of this antiplatelet activity by an antidote oligonucleotide (AO). Aptamer DTRI-031 exerts dose-dependent inhibition of platelet aggregation and thrombosis in whole blood and mice, respectively. Moreover, DTRI-031 can achieve potent vascular recanalization of platelet-rich thrombotic occlusions in murine and canine carotid arteries. Finally, DTRI-031 activity is rapidly (<5 min) and completely reversed by AO administration in a murine saphenous vein hemorrhage model, and murine toxicology studies indicate the aptamer is well tolerated. These findings suggest that targeting vWF with an antidote-controllable aptamer potentially represents an effective and safer treatment for thrombosis patients having platelet-rich arterial occlusions in the brain, heart, or periphery.

Full Text

Duke Authors

Cited Authors

  • Nimjee, SM; Dornbos, D; Pitoc, GA; Wheeler, DG; Layzer, JM; Venetos, N; Huttinger, A; Talentino, SE; Musgrave, NJ; Moody, H; Rempel, RE; Jones, C; Carlisle, K; Wilson, J; Bratton, C; Joseph, ME; Khan, S; Hoffman, MR; Sommerville, L; Becker, RC; Zweier, JL; Sullenger, BA

Published Date

  • July 3, 2019

Published In

Volume / Issue

  • 27 / 7

Start / End Page

  • 1228 - 1241

PubMed ID

  • 30987839

Pubmed Central ID

  • PMC6612779

Electronic International Standard Serial Number (EISSN)

  • 1525-0024

Digital Object Identifier (DOI)

  • 10.1016/j.ymthe.2019.03.016


  • eng

Conference Location

  • United States