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Promoting autophagy to mitigate coronavirus disease pathology in the elderly

In this commentary, we highlight autophagy's important function, while identifying potential therapeutic targets for severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) in the elderly. Autophagy's decline in the elderly causes increased cell senescence and a dysregulated immune sy...

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Detalles Bibliográficos
Autores principales: Lund Da Costa, Abby, Mehta, Het, Mathur, Ramkumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347787/
https://www.ncbi.nlm.nih.gov/pubmed/35942234
http://dx.doi.org/10.1002/ctd2.68
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author Lund Da Costa, Abby
Mehta, Het
Mathur, Ramkumar
author_facet Lund Da Costa, Abby
Mehta, Het
Mathur, Ramkumar
author_sort Lund Da Costa, Abby
collection PubMed
description In this commentary, we highlight autophagy's important function, while identifying potential therapeutic targets for severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) in the elderly. Autophagy's decline in the elderly causes increased cell senescence and a dysregulated immune system. As this demographic often faces decreased vaccine‐provided immunity, coronavirus disease 2019 treatments must be developed. We discuss a recent study by Acharya et al. (2022) that found that SF2523 induced autophagy, reducing SARS‐CoV‐2 replication. Furthermore, across varying dosages, SF2523 was shown to have a synergistic effect with remdesivir or MU‐UNMC. Consequently, we believe that SF2523, alone or with other anti‐virals, is a promising potential therapeutic for preventing SARS‐CoV‐2‐related mortalities.
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spelling pubmed-93477872022-08-04 Promoting autophagy to mitigate coronavirus disease pathology in the elderly Lund Da Costa, Abby Mehta, Het Mathur, Ramkumar Clin Transl Discov Commentary In this commentary, we highlight autophagy's important function, while identifying potential therapeutic targets for severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) in the elderly. Autophagy's decline in the elderly causes increased cell senescence and a dysregulated immune system. As this demographic often faces decreased vaccine‐provided immunity, coronavirus disease 2019 treatments must be developed. We discuss a recent study by Acharya et al. (2022) that found that SF2523 induced autophagy, reducing SARS‐CoV‐2 replication. Furthermore, across varying dosages, SF2523 was shown to have a synergistic effect with remdesivir or MU‐UNMC. Consequently, we believe that SF2523, alone or with other anti‐virals, is a promising potential therapeutic for preventing SARS‐CoV‐2‐related mortalities. John Wiley and Sons Inc. 2022-05-23 2022-06 /pmc/articles/PMC9347787/ /pubmed/35942234 http://dx.doi.org/10.1002/ctd2.68 Text en © 2022 The Authors. Clinical and Translational Discovery published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Lund Da Costa, Abby
Mehta, Het
Mathur, Ramkumar
Promoting autophagy to mitigate coronavirus disease pathology in the elderly
title Promoting autophagy to mitigate coronavirus disease pathology in the elderly
title_full Promoting autophagy to mitigate coronavirus disease pathology in the elderly
title_fullStr Promoting autophagy to mitigate coronavirus disease pathology in the elderly
title_full_unstemmed Promoting autophagy to mitigate coronavirus disease pathology in the elderly
title_short Promoting autophagy to mitigate coronavirus disease pathology in the elderly
title_sort promoting autophagy to mitigate coronavirus disease pathology in the elderly
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347787/
https://www.ncbi.nlm.nih.gov/pubmed/35942234
http://dx.doi.org/10.1002/ctd2.68
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