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Targeting immunometabolism to treat COVID-19
The COVID-19 crisis has emphasised the need for antiviral therapies to combat current and future viral zoonoses. Recent studies have shown that immune cells such as macrophages are the main contributors to the inflammatory response seen in the later inflammatory phase of COVID-19. Immune cells in th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195165/ https://www.ncbi.nlm.nih.gov/pubmed/34240083 http://dx.doi.org/10.1093/immadv/ltab013 |
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author | O’Carroll, Shane M O’Neill, Luke A J |
author_facet | O’Carroll, Shane M O’Neill, Luke A J |
author_sort | O’Carroll, Shane M |
collection | PubMed |
description | The COVID-19 crisis has emphasised the need for antiviral therapies to combat current and future viral zoonoses. Recent studies have shown that immune cells such as macrophages are the main contributors to the inflammatory response seen in the later inflammatory phase of COVID-19. Immune cells in the context of a viral infection such as SARS-CoV-2 undergo metabolic reprogramming to elicit these pro-inflammatory effector functions. The evidence of metabolic reprogramming in COVID-19 offers opportunities for metabolites with immunomodulatory properties to be investigated as potential therapies to combat this hyper-inflammatory response. Recent research indicates that the metabolite itaconate, previously known to be broadly antibacterial, may have both antiviral and immunomodulatory potential. Furthermore, low itaconate levels have shown to correlate with COVID-19 disease severity, potentially implicating its importance in the disease. The antiviral potential of itaconate has encouraged researchers to synthesise itaconate derivatives for antiviral screening, with some encouraging results. This review summarises the antiviral and immunomodulatory potential of immunometabolic modulators including metformin, peroxisome proliferator-activated receptor agonists and TEPP-46 as well as itaconate, and its derivatives and their potential use as broad spectrum anti-viral agents. |
format | Online Article Text |
id | pubmed-8195165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81951652021-06-15 Targeting immunometabolism to treat COVID-19 O’Carroll, Shane M O’Neill, Luke A J Immunother Adv Targeting Immunometabolism The COVID-19 crisis has emphasised the need for antiviral therapies to combat current and future viral zoonoses. Recent studies have shown that immune cells such as macrophages are the main contributors to the inflammatory response seen in the later inflammatory phase of COVID-19. Immune cells in the context of a viral infection such as SARS-CoV-2 undergo metabolic reprogramming to elicit these pro-inflammatory effector functions. The evidence of metabolic reprogramming in COVID-19 offers opportunities for metabolites with immunomodulatory properties to be investigated as potential therapies to combat this hyper-inflammatory response. Recent research indicates that the metabolite itaconate, previously known to be broadly antibacterial, may have both antiviral and immunomodulatory potential. Furthermore, low itaconate levels have shown to correlate with COVID-19 disease severity, potentially implicating its importance in the disease. The antiviral potential of itaconate has encouraged researchers to synthesise itaconate derivatives for antiviral screening, with some encouraging results. This review summarises the antiviral and immunomodulatory potential of immunometabolic modulators including metformin, peroxisome proliferator-activated receptor agonists and TEPP-46 as well as itaconate, and its derivatives and their potential use as broad spectrum anti-viral agents. Oxford University Press 2021-06-02 /pmc/articles/PMC8195165/ /pubmed/34240083 http://dx.doi.org/10.1093/immadv/ltab013 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Targeting Immunometabolism O’Carroll, Shane M O’Neill, Luke A J Targeting immunometabolism to treat COVID-19 |
title | Targeting immunometabolism to treat COVID-19 |
title_full | Targeting immunometabolism to treat COVID-19 |
title_fullStr | Targeting immunometabolism to treat COVID-19 |
title_full_unstemmed | Targeting immunometabolism to treat COVID-19 |
title_short | Targeting immunometabolism to treat COVID-19 |
title_sort | targeting immunometabolism to treat covid-19 |
topic | Targeting Immunometabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195165/ https://www.ncbi.nlm.nih.gov/pubmed/34240083 http://dx.doi.org/10.1093/immadv/ltab013 |
work_keys_str_mv | AT ocarrollshanem targetingimmunometabolismtotreatcovid19 AT oneilllukeaj targetingimmunometabolismtotreatcovid19 |