Antiviral Properties of the NSAID Drug Naproxen Targeting the Nucleoprotein of SARS-CoV-2 Coronavirus.
Olivier TerrierSébastien DillyAndrés PizzornoDominika ChalupskaJana HumpolickovaEvžen BouřaFrancis BerenbaumStéphane QuideauBruno LinaBruno FèveFrédéric AdnetMichèle SabbahManuel Rosa-CalatravaVincent MaréchalJulien HenriAnny Slama-SchwokPublished in: Molecules (Basel, Switzerland) (2021)
There is an urgent need for specific antiviral treatments directed against SARS-CoV-2 to prevent the most severe forms of COVID-19. By drug repurposing, affordable therapeutics could be supplied worldwide in the present pandemic context. Targeting the nucleoprotein N of the SARS-CoV-2 coronavirus could be a strategy to impede viral replication and possibly other essential functions associated with viral N. The antiviral properties of naproxen, a non-steroidal anti-inflammatory drug (NSAID) that was previously demonstrated to be active against Influenza A virus, were evaluated against SARS-CoV-2. Intrinsic fluorescence spectroscopy, fluorescence anisotropy, and dynamic light scattering assays demonstrated naproxen binding to the nucleoprotein of SARS-Cov-2 as predicted by molecular modeling. Naproxen impeded recombinant N oligomerization and inhibited viral replication in infected cells. In VeroE6 cells and reconstituted human primary respiratory epithelium models of SARS-CoV-2 infection, naproxen specifically inhibited viral replication and protected the bronchial epithelia against SARS-CoV-2-induced damage. No inhibition of viral replication was observed with paracetamol or the COX-2 inhibitor celecoxib. Thus, among the NSAID tested, only naproxen combined antiviral and anti-inflammatory properties. Naproxen addition to the standard of care could be beneficial in a clinical setting, as tested in an ongoing clinical study.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- anti inflammatory
- induced apoptosis
- single molecule
- drug induced
- endothelial cells
- cell cycle arrest
- emergency department
- palliative care
- small molecule
- high resolution
- endoplasmic reticulum stress
- cancer therapy
- early onset
- drug delivery
- high glucose
- quality improvement
- high density
- pain management
- energy transfer
- pluripotent stem cells