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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2022
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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. |
format | Online Article Text |
id | pubmed-9108900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
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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