Affinity-based design of a synthetic universal reversal agent for heparin anticoagulants

Rajesh A. Shenoi, Manu Thomas Kalathottukaren, Richard J. Travers, Benjamin F L Lai, A. Louise Creagh, Dirk Lange, Kai Yu, Marie Weinhart, Ben H. Chew, Caigan Du, Donald E. Brooks, Cedric J. Carter, James H. Morrissey, Charles A. Haynes, Jayachandran N. Kizhakkedathu

Research output: Contribution to journalArticlepeer-review

Abstract

Heparin-based anticoagulant drugs have been widely used for the prevention of blood clotting during surgical procedures and for the treatment of thromboembolic events. However, bleeding risks associated with these anticoagulants demand continuous monitoring and neutralization with suitable antidotes. Protamine, the only clinically approved antidote to heparin, has shown adverse effects and ineffectiveness against low-molecular weight heparins and fondaparinux, a heparin-related medication. Alternative approaches based on cationic molecules and recombinant proteins have several drawbacks including limited efficacy, toxicity, immunogenicity, and high cost. Thus, there is an unmet clinical need for safer, rapid, predictable, and cost-effective anticoagulant-reversal agents for all clinically used heparins. We report a design strategy for a fully synthetic dendritic polymer-based universal heparin reversal agent (UHRA) that makes use of multivalent presentation of branched cationic heparin binding groups (HBGs). Optimization of the UHRA design was aided by isothermal titration calorimetry studies, biocompatibility evaluation, and heparin neutralization analysis. By controlling the scaffold's molecular weight, the nature of the protective shell, and the presentation of HBGs on the polymer scaffold, we arrived at lead UHRA molecules that completely neutralized the activity of all clinically used heparins. The optimized UHRA molecules demonstrated superior efficacy and safety profiles and mitigated heparin-induced bleeding in animal models. This new polymer therapeutic may benefit patients undergoing high-risk surgical procedures and has potential for the treatment of anticoagulantrelated bleeding problems.

Original languageEnglish (US)
Article number260ra150
JournalScience Translational Medicine
Volume6
Issue number260
DOIs
StatePublished - Oct 29 2014

ASJC Scopus subject areas

  • General Medicine

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