Recombinant hirudin in clinical practice: focus on lepirudin
Review published in Circulation (2001)
Abstract
Clinical applications for recombinant hirudins have been investigated for the past 10 years. The first indication for which a hirudin-lepirudin-has been approved is treatment of heparin-induced thrombocytopenia (HIT). Also, the recently completed trials for use of lepirudin in unstable angina indicate a potentially new indication. This review describes pharmacology and clinical applications of lepirudin with an emphasis on HIT and unstable angina. An overview of usage of lepirudin in acute coronary syndromes is given, as well as a summary of rare indications for lepirudin, such as extracorporeal circulation, for which comprehensive data are lacking.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Summary
This review covers lepirudin, the first approved recombinant hirudin, for heparin-induced thrombocytopenia, its pharmacology, completed unstable angina trials suggesting a new indication, acute coronary syndrome use, and rare applications such as extracorporeal circulation where comprehensive data are lacking.
Why This Matters for Hirudotherapy
This review describes the pharmacology and clinical use of recombinant hirudin, focusing on lepirudin, and notes that the first approved indication was treatment of heparin-induced thrombocytopenia (HIT), with completed trials in unstable angina pointing to a potential further indication and additional coverage of acute coronary syndromes and sparse data for uses such as extracorporeal circulation. It documents the medicinal-leech-to-medicine story: hirudin, the leech's natural thrombin inhibitor, was re-engineered as a recombinant drug (lepirudin) and entered routine clinical anticoagulation, an example of how the leech secretome has yielded approved therapeutics. As a narrative review it summarizes others' trials rather than presenting new primary data, and it describes the therapeutic recombinant molecule, not whole-leech hirudotherapy; it also predates lepirudin's later market withdrawal, so it reflects the state of practice circa 2001.
Citation
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