Американское общество гирудотерапии

Efficacy and safety of next-generation tick transcriptome-derived direct thrombin inhibitors

Translational study published in Nature Communications (2021)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Preclinical (animal)Разработка лекарственных препаратовГеномика и протеомикаФармакология секрета слюнных желёзKoh CY et al. · Nature Communications, 2021

Abstract

Despite their limitations, unfractionated heparin (UFH) and bivalirudin remain standard-of-care parenteral anticoagulants for percutaneous coronary intervention (PCI). We discovered novel direct thrombin inhibitors (DTIs) from tick salivary transcriptomes and optimised their pharmacologic activity. The most potent, ultravariegin, inhibits thrombin with a Ki of 4.0 pM, 445-fold better than bivalirudin. Unexpectedly, despite their greater antithrombotic effect, variegin/ultravariegin demonstrated less bleeding, achieving a 3-to-7-fold wider therapeutic index in rodent thrombosis and bleeding models. When used in combination with aspirin and ticagrelor in a porcine model, variegin/ultravariegin reduced stent thrombosis compared with antiplatelet therapy alone but achieved a 5-to-7-fold lower bleeding time than UFH/bivalirudin. Moreover, two antibodies screened from a naïve human antibody library effectively reversed the anticoagulant activity of ultravariegin, demonstrating proof-of-principle for antidote reversal. Variegin and ultravariegin are promising translational candidates for next-generation DTIs that may reduce peri-PCI bleeding in the presence of antiplatelet therapy.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleResearch Support, Non-U.S. Gov't
Indexed MeSH termsAmblyommaAnimalsAntibodiesAnticoagulantsAntidotesAntithrombinsAspirinDrug DevelopmentDrug DiscoveryFemaleFibrinolytic AgentsGene Library

Резюме

Ultravariegin from tick salivary transcriptomes inhibits thrombin with a Ki of 4.0 pM (445-fold better than bivalirudin), achieves 3-to-7-fold wider therapeutic index than UFH/bivalirudin in rodent and porcine models, and is antibody-reversible.

Почему это важно для гирудотерапии

This study describes the discovery and optimization of novel direct thrombin inhibitors (variegin and ultravariegin) derived from tick salivary transcriptomes, not from leeches. Ultravariegin inhibits thrombin with a Ki of 4.0 pM (445-fold better than bivalirudin) and demonstrated a 3-to-7-fold wider therapeutic index in rodent thrombosis and bleeding models, with reduced stent thrombosis and shorter bleeding times in a porcine model using aspirin and ticagrelor; two human antibodies reversed its activity as proof-of-principle antidotes. For ASH, the relevance is indirect: while no leeches are involved, this work pertains to hematophagous-animal-derived anticoagulants, a domain overlapping with leech-derived therapeutics. CAVEAT: This study involves no leeches or leech-derived compounds; all data are preclinical (rodent and porcine models), and relevance to hirudotherapy is strictly conceptual.

Цитирование

Efficacy and safety of next-generation tick transcriptome-derived direct thrombin inhibitors.

Koh CY et al. · Nature Communications, 2021

Связанный клинический контекст

Добавлено в библиотеку ASH: May 27, 2026 · Последнее обновление сайта: June 18, 2026

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