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Mol Ther ; 32(7): 2286-2298, 2024 Jul 03.
Article in English | MEDLINE | ID: mdl-38720458

ABSTRACT

Injectable anticoagulants are widely used in medical procedures to prevent unwanted blood clotting. However, many lack safe, effective reversal agents. Here, we present new data on a previously described RNA origami-based, direct thrombin inhibitor (HEX01). We describe a new, fast-acting, specific, single-molecule reversal agent (antidote) and present in vivo data for the first time, including efficacy, reversibility, preliminary safety, and initial biodistribution studies. HEX01 contains multiple thrombin-binding aptamers appended on an RNA origami. It exhibits excellent anticoagulation activity in vitro and in vivo. The new single-molecule, DNA antidote (HEX02) reverses anticoagulation activity of HEX01 in human plasma within 30 s in vitro and functions effectively in a murine liver laceration model. Biodistribution studies of HEX01 in whole mice using ex vivo imaging show accumulation mainly in the liver over 24 h and with 10-fold lower concentrations in the kidneys. Additionally, we show that the HEX01/HEX02 system is non-cytotoxic to epithelial cell lines and non-hemolytic in vitro. Furthermore, we found no serum cytokine response to HEX01/HEX02 in a murine model. HEX01 and HEX02 represent a safe and effective coagulation control system with a fast-acting, specific reversal agent showing promise for potential drug development.


Subject(s)
Aptamers, Nucleotide , Thrombin , Animals , Mice , Humans , Aptamers, Nucleotide/pharmacology , Aptamers, Nucleotide/chemistry , Thrombin/metabolism , Blood Coagulation/drug effects , Tissue Distribution , RNA , Disease Models, Animal , Liver/metabolism , Liver/drug effects , Anticoagulants/pharmacology , Anticoagulants/chemistry , Antithrombins/pharmacology , Antidotes/pharmacology , Antidotes/chemistry
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