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Inhibition of SARS-CoV-2 Infection by the Cyclophilin Inhibitor Alisporivir (Debio 025)

Authors :
Rozenn Brillet
Margot Morin-Dewaele
Patrice Bruscella
Nazim Ahnou
Jean-Michel Pawlotsky
Abdelhakim Ahmed-Belkacem
François Berry
Laurent Softic
Slim Fourati
Sabah Hamadat
Quentin Nevers
Molecular virology and immunology – Physiopathology and therapeutic of chronic viral hepatitis (Team 18) (Inserm U955)
Institut Mondor de Recherche Biomédicale (IMRB)
Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Hôpital Henri Mondor
Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)
Bruscella, Patrice
Source :
Antimicrobial Agents and Chemotherapy, Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2020, 64 (7), pp.e00876-20. ⟨10.1128/AAC.00876-20⟩
Publication Year :
2020
Publisher :
American Society for Microbiology, 2020.

Abstract

Cyclophilins play a key role in the life cycle of coronaviruses. Alisporivir (Debio 025) is a nonimmunosuppressive analogue of cyclosporine with potent cyclophilin inhibition properties. Alisporivir reduced SARS-CoV-2 RNA production in a dose-dependent manner in Vero E6 cells, with a 50% effective concentration (EC50) of 0.46 ± 0.04 μM. Alisporivir inhibited a postentry step of the SARS-CoV-2 life cycle. These results justify rapidly conducting a proof-of-concept phase 2 trial with alisporivir in patients with SARS-CoV-2 infection.

Details

ISSN :
10986596 and 00664804
Volume :
64
Database :
OpenAIRE
Journal :
Antimicrobial Agents and Chemotherapy
Accession number :
edsair.doi.dedup.....776540f11a5c3121763b292e8a2943b7
Full Text :
https://doi.org/10.1128/aac.00876-20