Clofoctol inhibits SARS-CoV-2 replication and reduces lung pathology in mice.
Sandrine BelouzardArnaud MachelartValentin SencioThibaut VausselinEik HoffmannNathalie DeboosereYves RouilléLowiese DesmaretsKarin SéronAdeline DanneelsCyril RobilLoic BelloyCamille MoreauCatherine PiveteauAlexandre BielaAlexandre VandeputteSéverine HeumelLucie DeruyterJulie DumontFlorence LerouxIlka EngelmannEnagnon Kazali AlidjinouDidier HoberPriscille BrodinTerence BeghynFrançois TrotteinBenoit DeprezJean DubuissonPublished in: PLoS pathogens (2022)
Drug repurposing has the advantage of shortening regulatory preclinical development steps. Here, we screened a library of drug compounds, already registered in one or several geographical areas, to identify those exhibiting antiviral activity against SARS-CoV-2 with relevant potency. Of the 1,942 compounds tested, 21 exhibited a substantial antiviral activity in Vero-81 cells. Among them, clofoctol, an antibacterial drug used for the treatment of bacterial respiratory tract infections, was further investigated due to its favorable safety profile and pharmacokinetic properties. Notably, the peak concentration of clofoctol that can be achieved in human lungs is more than 20 times higher than its IC50 measured against SARS-CoV-2 in human pulmonary cells. This compound inhibits SARS-CoV-2 at a post-entry step. Lastly, therapeutic treatment of human ACE2 receptor transgenic mice decreased viral load, reduced inflammatory gene expression and lowered pulmonary pathology. Altogether, these data strongly support clofoctol as a therapeutic candidate for the treatment of COVID-19 patients.
Keyphrases
- sars cov
- endothelial cells
- gene expression
- respiratory syndrome coronavirus
- induced apoptosis
- pulmonary hypertension
- respiratory tract
- emergency department
- dna methylation
- oxidative stress
- adipose tissue
- type diabetes
- signaling pathway
- cell death
- stem cells
- metabolic syndrome
- cell proliferation
- angiotensin ii
- adverse drug
- deep learning
- bone marrow
- smoking cessation
- drug induced
- high speed
- single molecule
- cell therapy
- atomic force microscopy