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Emerging applications of aptamers for anticoagulation and hemostasis

Chabata, Charlene V.a,b; Frederiksen, James W.b; Sullenger, Bruce A.a,b; Gunaratne, Ruwana,b,c

doi: 10.1097/MOH.0000000000000452
HEMOSTASIS AND THROMBOSIS: Edited by Alvin H. Schmaier

Purpose of review Since the selection of the first thrombin-binding aptamer in 1992, the use of nucleic acid aptamers to target specific coagulation factors has emerged as a valuable approach for generating novel anticoagulant and procoagulant therapeutics. Herein, we highlight the most recent discoveries involving application of aptamers for those purposes.

Recent findings Learning from the successes and pitfalls of the FIXa-targeting aptamer pegnivacogin in preclinical and clinical studies, the latest efforts to develop antidote-controllable anticoagulation strategies for cardiopulmonary bypass that avoid unfractionated heparin involve potentiation of the exosite-binding factor X (FX)a aptamer 11F7t by combination with either a small molecule FXa catalytic site inhibitor or a thrombin aptamer. Recent work has also focused on identifying aptamer inhibitors of contact pathway factors such as FXIa and kallikrein, which may prove to be well tolerated and effective antithrombotic agents in certain clinical settings. Finally, new approaches to develop procoagulant aptamers to control bleeding associated with hemophilia and other coagulopathies involve targeting activated protein C and tissue plasminogen activator.

Summary Overall, these recent findings exemplify the versatility of aptamers to modulate a variety of procoagulant and anticoagulant factors, along with their capacity to be used complementarily with other aptamers or drugs for wide-ranging applications.

aDepartment of Pharmacology and Cancer Biology

bDepartment of Surgery

cMedical Scientist Training Program, Duke University, Durham, North Carolina, USA

Correspondence to Ruwan Gunaratne, 1045 MSRB II, Box 103035, Durham, NC 27710, USA. Tel: +1 919 684 4822. E-mail: ruwan.gunaratne@duke.edu

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