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Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection

Recurrent waves of COVID19 remain a major global health concern. Repurposing either FDA-approved or clinically advanced drug candidates can save time and effort required for validating the safety profile and FDA approval. However, the selection of appropriate screening approaches is key to identifyi...

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Autores principales: Kumar, Prabhakaran, Mathayan, Manikannan, Smieszek, Sandra P., Przychodzen, Bartlomiej P., Koprivica, Vuk, Birznieks, Gunther, Polymeropoulos, Mihael H., Prabhakar, Bellur S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108900/
https://www.ncbi.nlm.nih.gov/pubmed/35598394
http://dx.doi.org/10.1016/j.virol.2022.05.004
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author Kumar, Prabhakaran
Mathayan, Manikannan
Smieszek, Sandra P.
Przychodzen, Bartlomiej P.
Koprivica, Vuk
Birznieks, Gunther
Polymeropoulos, Mihael H.
Prabhakar, Bellur S.
author_facet Kumar, Prabhakaran
Mathayan, Manikannan
Smieszek, Sandra P.
Przychodzen, Bartlomiej P.
Koprivica, Vuk
Birznieks, Gunther
Polymeropoulos, Mihael H.
Prabhakar, Bellur S.
author_sort Kumar, Prabhakaran
collection PubMed
description Recurrent waves of COVID19 remain a major global health concern. Repurposing either FDA-approved or clinically advanced drug candidates can save time and effort required for validating the safety profile and FDA approval. However, the selection of appropriate screening approaches is key to identifying novel candidate drugs with a higher probability of clinical success. Here, we report a rapid, stratified two-step screening approach using pseudovirus entry inhibition assay followed by an infectious prototypic SARS CoV2 cytotoxic effect inhibition assay in multiple cell lines. Using this approach, we screened a library of FDA-approved and clinical-stage drugs and identified four compounds, apilimod, berbamine, cepharanthine and (S)-crizotinib which potently inhibited SARS CoV2-induced cell death. Importantly, these drugs exerted similar inhibitory effect on the delta and omicron variants although they replicated less efficiently than the prototypic strain. Apilimod is currently under clinical trial (NCT04446377) for COVID19 supporting the validity and robustness of our screening approach.
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spelling pubmed-91089002022-05-16 Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection Kumar, Prabhakaran Mathayan, Manikannan Smieszek, Sandra P. Przychodzen, Bartlomiej P. Koprivica, Vuk Birznieks, Gunther Polymeropoulos, Mihael H. Prabhakar, Bellur S. Virology Brief Communication Recurrent waves of COVID19 remain a major global health concern. Repurposing either FDA-approved or clinically advanced drug candidates can save time and effort required for validating the safety profile and FDA approval. However, the selection of appropriate screening approaches is key to identifying novel candidate drugs with a higher probability of clinical success. Here, we report a rapid, stratified two-step screening approach using pseudovirus entry inhibition assay followed by an infectious prototypic SARS CoV2 cytotoxic effect inhibition assay in multiple cell lines. Using this approach, we screened a library of FDA-approved and clinical-stage drugs and identified four compounds, apilimod, berbamine, cepharanthine and (S)-crizotinib which potently inhibited SARS CoV2-induced cell death. Importantly, these drugs exerted similar inhibitory effect on the delta and omicron variants although they replicated less efficiently than the prototypic strain. Apilimod is currently under clinical trial (NCT04446377) for COVID19 supporting the validity and robustness of our screening approach. Academic Press 2022-07 2022-05-16 /pmc/articles/PMC9108900/ /pubmed/35598394 http://dx.doi.org/10.1016/j.virol.2022.05.004 Text en Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Brief Communication
Kumar, Prabhakaran
Mathayan, Manikannan
Smieszek, Sandra P.
Przychodzen, Bartlomiej P.
Koprivica, Vuk
Birznieks, Gunther
Polymeropoulos, Mihael H.
Prabhakar, Bellur S.
Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection
title Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection
title_full Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection
title_fullStr Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection
title_full_unstemmed Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection
title_short Identification of potential COVID-19 treatment compounds which inhibit SARS Cov2 prototypic, Delta and Omicron variant infection
title_sort identification of potential covid-19 treatment compounds which inhibit sars cov2 prototypic, delta and omicron variant infection
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108900/
https://www.ncbi.nlm.nih.gov/pubmed/35598394
http://dx.doi.org/10.1016/j.virol.2022.05.004
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