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Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses
The increasingly frequent outbreaks of pathogenic viruses have underlined the urgent need to improve our arsenal of antivirals that can be deployed for future pandemics. Innate immunity is a powerful first line of defense against pathogens, and compounds that boost the innate response have high pote...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213012/ https://www.ncbi.nlm.nih.gov/pubmed/35728599 http://dx.doi.org/10.1016/j.chembiol.2022.05.009 |
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author | Maarifi, Ghizlane Martin, Marie-France Zebboudj, Abderezak Boulay, Aude Nouaux, Pierre Fernandez, Juliette Lagisquet, Justine Garcin, Dominique Gaudin, Raphael Arhel, Nathalie J. Nisole, Sébastien |
author_facet | Maarifi, Ghizlane Martin, Marie-France Zebboudj, Abderezak Boulay, Aude Nouaux, Pierre Fernandez, Juliette Lagisquet, Justine Garcin, Dominique Gaudin, Raphael Arhel, Nathalie J. Nisole, Sébastien |
author_sort | Maarifi, Ghizlane |
collection | PubMed |
description | The increasingly frequent outbreaks of pathogenic viruses have underlined the urgent need to improve our arsenal of antivirals that can be deployed for future pandemics. Innate immunity is a powerful first line of defense against pathogens, and compounds that boost the innate response have high potential to act as broad-spectrum antivirals. Here, we harnessed localization-dependent protein-complementation assays (called Alpha Centauri) to measure the nuclear translocation of interferon regulatory factors (IRFs), thus providing a readout of innate immune activation following viral infection that is applicable to high-throughput screening of immunomodulatory molecules. As proof of concept, we screened a library of kinase inhibitors on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and identified Gilteritinib as a powerful enhancer of innate responses to viral infection. This immunostimulatory activity of Gilteritinib was found to be dependent on the AXL-IRF7 axis and results in a broad and potent antiviral activity against unrelated RNA viruses. |
format | Online Article Text |
id | pubmed-9213012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Author(s). Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92130122022-06-22 Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses Maarifi, Ghizlane Martin, Marie-France Zebboudj, Abderezak Boulay, Aude Nouaux, Pierre Fernandez, Juliette Lagisquet, Justine Garcin, Dominique Gaudin, Raphael Arhel, Nathalie J. Nisole, Sébastien Cell Chem Biol Article The increasingly frequent outbreaks of pathogenic viruses have underlined the urgent need to improve our arsenal of antivirals that can be deployed for future pandemics. Innate immunity is a powerful first line of defense against pathogens, and compounds that boost the innate response have high potential to act as broad-spectrum antivirals. Here, we harnessed localization-dependent protein-complementation assays (called Alpha Centauri) to measure the nuclear translocation of interferon regulatory factors (IRFs), thus providing a readout of innate immune activation following viral infection that is applicable to high-throughput screening of immunomodulatory molecules. As proof of concept, we screened a library of kinase inhibitors on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and identified Gilteritinib as a powerful enhancer of innate responses to viral infection. This immunostimulatory activity of Gilteritinib was found to be dependent on the AXL-IRF7 axis and results in a broad and potent antiviral activity against unrelated RNA viruses. The Author(s). Published by Elsevier Ltd. 2022-07-21 2022-06-20 /pmc/articles/PMC9213012/ /pubmed/35728599 http://dx.doi.org/10.1016/j.chembiol.2022.05.009 Text en © 2022 The Author(s) 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 | Article Maarifi, Ghizlane Martin, Marie-France Zebboudj, Abderezak Boulay, Aude Nouaux, Pierre Fernandez, Juliette Lagisquet, Justine Garcin, Dominique Gaudin, Raphael Arhel, Nathalie J. Nisole, Sébastien Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
title | Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
title_full | Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
title_fullStr | Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
title_full_unstemmed | Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
title_short | Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
title_sort | identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213012/ https://www.ncbi.nlm.nih.gov/pubmed/35728599 http://dx.doi.org/10.1016/j.chembiol.2022.05.009 |
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