Unfractionated heparin inhibits live wild type SARS-CoV-2 cell infectivity at therapeutically relevant concentrations



Tree, Julia A, Turnbull, Jeremy E ORCID: 0000-0002-1791-754X, Buttigieg, Karen R, Elmore, Michael J, Coombes, Naomi, Hogwood, John, Mycroft-West, Courtney J, Lima, Marcelo A, Skidmore, Mark A, Karlsson, Richard
et al (show 10 more authors) (2021) Unfractionated heparin inhibits live wild type SARS-CoV-2 cell infectivity at therapeutically relevant concentrations. BRITISH JOURNAL OF PHARMACOLOGY, 178 (3). pp. 626-635.

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Abstract

<h4>Background and purpose</h4>Currently, there are no licensed vaccines and limited antivirals for the treatment of COVID-19. Heparin (delivered systemically) is currently used to treat anticoagulant anomalies in COVID-19 patients. Additionally, in the United Kingdom, Brazil and Australia, nebulised unfractionated heparin (UFH) is being trialled in COVID-19 patients as a potential treatment. A systematic comparison of the potential antiviral effect of various heparin preparations on live wild type SARS-CoV-2, in vitro, is needed.<h4>Experimental approach</h4>Seven different heparin preparations including UFH and low MW heparins (LMWH) of porcine or bovine origin were screened for antiviral activity against live SARS-CoV-2 (Australia/VIC01/2020) using a plaque inhibition assay with Vero E6 cells. Interaction of heparin with spike protein RBD was studied using differential scanning fluorimetry and the inhibition of RBD binding to human ACE2 protein using elisa assays was examined.<h4>Key results</h4>All the UFH preparations had potent antiviral effects, with IC<sub>50</sub> values ranging between 25 and 41 μg·ml<sup>-1</sup> , whereas LMWHs were less inhibitory by ~150-fold (IC<sub>50</sub> range 3.4-7.8 mg·ml<sup>-1</sup> ). Mechanistically, we observed that heparin binds and destabilizes the RBD protein and furthermore, we show heparin directly inhibits the binding of RBD to the human ACE2 protein receptor.<h4>Conclusion and implications</h4>This comparison of clinically relevant heparins shows that UFH has significantly stronger SARS-CoV-2 antiviral activity compared to LMWHs. UFH acts to directly inhibit binding of spike protein to the human ACE2 protein receptor. Overall, the data strongly support further clinical investigation of UFH as a potential treatment for patients with COVID-19.

Item Type: Article
Uncontrolled Keywords: COVID-19, heparin, LMWH, nebulised, SARS-CoV-2, UFH
Divisions: Faculty of Health and Life Sciences
Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology
Depositing User: Symplectic Admin
Date Deposited: 31 Mar 2021 15:16
Last Modified: 18 Jan 2023 22:54
DOI: 10.1111/bph.15304
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3118230