Increased Plasma Heparanase Activity in COVID-19 Patients

Baranca Buijsers(Radboud Institute for Molecular Life Sciences), Cansu Yanginlar(Radboud Institute for Molecular Life Sciences), Aline de Nooijer(Radboud University Nijmegen), Inge Grondman(Radboud University Medical Center), Marissa L. Maciej-Hulme(Radboud Institute for Molecular Life Sciences), Inge Jonkman(Radboud University Nijmegen), Nico Janssen(Radboud University Medical Center), Nils Rother(Radboud University Medical Center), Mark de Graaf(Radboud Institute for Molecular Life Sciences), Peter Pickkers(Radboud University Nijmegen), Matthijs Kox(Radboud University Nijmegen), Leo A. B. Joosten(Radboud University Medical Center), Tom Nijenhuis(Radboud University Medical Center), Mihai G. Netea(Radboud University Medical Center), Luuk B. Hilbrands(Radboud Institute for Molecular Life Sciences), Frank L. van de Veerdonk(Radboud University Medical Center), Raphaël Duivenvoorden(Radboud University Medical Center), Quirijn de Mast(Radboud University Nijmegen), Johan van der Vlag(Radboud University Nijmegen)
Frontiers in Immunology
October 6, 2020
Cited by 135Open Access
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Abstract

Reports suggest a role of endothelial dysfunction and loss of endothelial barrier function in COVID-19. It is well established that the endothelial glycocalyx-degrading enzyme heparanase contributes to vascular leakage and inflammation. Low molecular weight heparins (LMWH) serve as an inhibitor of heparanase. We hypothesize that heparanase contributes to the pathogenesis of COVID-19, and that heparanase may be inhibited by LMWH. To test this hypothesis, heparanase activity and heparan sulfate levels were measured in plasma of healthy controls (n = 10) and COVID-19 patients (n = 48). Plasma heparanase activity and heparan sulfate levels were significantly elevated in COVID-19 patients. Heparanase activity was associated with disease severity including the need for intensive care, lactate dehydrogenase levels, and creatinine levels. Use of prophylactic LMWH in non-ICU patients was associated with a reduced heparanase activity. Since there is no other clinically applied heparanase inhibitor currently available, therapeutic treatment of COVID-19 patients with low molecular weight heparins should be explored.


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