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Development and optimisation of a high-throughput screening assay for in vitro anti-SARS-CoV-2 activity: evaluation of 5676 phase 1 passed structures
Winston Chiu; Lore Verschueren; Christel Van den Eynde; Christophe Buyck; Sandra De Meyer; Dirk Jochmans; Denisa Bojkova; Sandra Ciesek; Jindrich Cinatl; Steven De Jonghe; Pieter Leyssen; Johan Neyts; Marnix Van Loock; Ellen Van Damme.
Affiliation
  • Winston Chiu; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy
  • Lore Verschueren; Janssen Pharmaceutica NV
  • Christel Van den Eynde; Janssen Pharmaceutica NV
  • Christophe Buyck; Janssen Pharmaceutica NV
  • Sandra De Meyer; Janssen Pharmaceutica NV
  • Dirk Jochmans; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy
  • Denisa Bojkova; Institute of Medical Virology, University Hospital Frankfurt, Goethe University
  • Sandra Ciesek; Institute of Medical Virology, University Hospital Frankfurt, Goethe University
  • Jindrich Cinatl; Institute of Medical Virology, University Hospital Frankfurt, Goethe University
  • Steven De Jonghe; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy
  • Pieter Leyssen; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy
  • Johan Neyts; KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy
  • Marnix Van Loock; Janssen Pharmaceutica NV
  • Ellen Van Damme; Janssen Pharmaceutica NV
Preprint in English | bioRxiv | ID: ppbiorxiv-478671
ABSTRACT
Although vaccines are currently used to control the coronavirus disease 2019 (COVID-19) pandemic, treatment options are urgently needed for those who cannot be vaccinated and for future outbreaks involving new severe acute respiratory syndrome coronavirus virus 2 (SARS-CoV-2) strains or coronaviruses not covered by current vaccines. Thus far, few existing antivirals are known to be effective against SARS-CoV-2 and clinically successful against COVID-19. As part of an immediate response to the COVID-19 pandemic, a high-throughput, high content imaging-based SARS-CoV-2 infection assay was developed in VeroE6-eGFP cells and was used to screen a library of 5676 compounds that passed phase 1 clinical trials. Eight candidates (nelfinavir, RG-12915, itraconazole, chloroquine, hydroxychloroquine, sematilide, remdesivir, and doxorubicin) with in vitro anti-SARS-CoV-2 activity in VeroE6-eGFP and/or Caco-2 cell lines were identified. However, apart from remdesivir, toxicity and pharmacokinetic data did not support further clinical development of these compounds for COVID-19 treatment.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Experimental_studies / Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Experimental_studies / Prognostic study Language: English Year: 2022 Document type: Preprint
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