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Clofoctol inhibits SARS-CoV-2 replication and reduces lung pathology in mice.
Belouzard, Sandrine; Machelart, Arnaud; Sencio, Valentin; Vausselin, Thibaut; Hoffmann, Eik; Deboosere, Nathalie; Rouillé, Yves; Desmarets, Lowiese; Séron, Karin; Danneels, Adeline; Robil, Cyril; Belloy, Loic; Moreau, Camille; Piveteau, Catherine; Biela, Alexandre; Vandeputte, Alexandre; Heumel, Séverine; Deruyter, Lucie; Dumont, Julie; Leroux, Florence; Engelmann, Ilka; Alidjinou, Enagnon Kazali; Hober, Didier; Brodin, Priscille; Beghyn, Terence; Trottein, François; Deprez, Benoit; Dubuisson, Jean.
  • Belouzard S; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Machelart A; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Sencio V; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Vausselin T; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Hoffmann E; APTEEUS, Campus Pasteur Lille, Lille, France.
  • Deboosere N; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Rouillé Y; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Desmarets L; Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, Plateformes lilloises en biologie et santé, Lille, France.
  • Séron K; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Danneels A; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Robil C; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Belloy L; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Moreau C; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Piveteau C; APTEEUS, Campus Pasteur Lille, Lille, France.
  • Biela A; APTEEUS, Campus Pasteur Lille, Lille, France.
  • Vandeputte A; Univ Lille, Inserm, Institut Pasteur de Lille, Drugs and Molecules for Living Systems, Lille, France.
  • Heumel S; Univ Lille, Inserm, Institut Pasteur de Lille, Drugs and Molecules for Living Systems, Lille, France.
  • Deruyter L; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Dumont J; Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, Plateformes lilloises en biologie et santé, Lille, France.
  • Leroux F; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Engelmann I; Univ Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, Lille, France.
  • Alidjinou EK; Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, Plateformes lilloises en biologie et santé, Lille, France.
  • Hober D; Univ Lille, Inserm, Institut Pasteur de Lille, Drugs and Molecules for Living Systems, Lille, France.
  • Brodin P; Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, Plateformes lilloises en biologie et santé, Lille, France.
  • Beghyn T; Univ Lille, Inserm, Institut Pasteur de Lille, Drugs and Molecules for Living Systems, Lille, France.
  • Trottein F; Univ Lille, CHU Lille, Laboratoire de Virologie, Lille, France.
  • Deprez B; Univ Lille, CHU Lille, Laboratoire de Virologie, Lille, France.
  • Dubuisson J; Univ Lille, CHU Lille, Laboratoire de Virologie, Lille, France.
PLoS Pathog ; 18(5): e1010498, 2022 05.
Article en En | MEDLINE | ID: mdl-35587469
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: SARS-CoV-2 / Tratamiento Farmacológico de COVID-19 Límite: Animals / Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: SARS-CoV-2 / Tratamiento Farmacológico de COVID-19 Límite: Animals / Humans Idioma: En Año: 2022 Tipo del documento: Article