Semin Thromb Hemost 1996; 22(2): 185-196
DOI: 10.1055/s-2007-999007
Copyright © 1996 by Thieme Medical Publishers, Inc.

Hirudins: From Leeches to Man

Robert B. Wallis
  • From Biopharm (UK) Ltd, Bryngelen Manor, Hendy, Dyfed, United Kingdom.
Further Information

Publication History

Publication Date:
06 February 2008 (online)

Abstract

Hirudins are a group of highly homologous polypeptides from the medicinal leech, Hirudo medicinalis. They have an extremely high and specific affinity for thrombin and are consequently potent anticoagulants. They inhibit platelet aggregation induced by thrombin and efficiently inhibit thrombin when it is bound to a fibrin clot. Recombinant hirudins have now been produced and have been used to show a wide range of effects on thrombosis in animal models. They are particularly effective against venoustype thrombi and have greater effects than heparins on the platelet-rich thrombi in arteries. Recombinant hirudins are currently undergoing clinical trials in deep venous thrombosis and acute coronary syndrome and as an adjunct to thrombolysis in myocardial infarction. Results from pilot trials indicate promising advantages over the currently used antithrombotic agents. Larger clinical trials have been initiated and we await with great interest their imminent publication.