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Chemokine Regulation During Epidemic Coronavirus Infection

SARS-CoV-2 (Severe Acute Respiratory Syndrome coronavirus-2) is the third coronavirus to emerge as a cause of severe and frequently fatal pneumonia epidemics in humans, joining SARS-CoV and MERS-CoV (Middle East Respiratory Syndrome-coronavirus). As with many infectious diseases, the immune response...

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Autores principales: Majumdar, Shamik, Murphy, Philip M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890195/
https://www.ncbi.nlm.nih.gov/pubmed/33613280
http://dx.doi.org/10.3389/fphar.2020.600369
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author Majumdar, Shamik
Murphy, Philip M.
author_facet Majumdar, Shamik
Murphy, Philip M.
author_sort Majumdar, Shamik
collection PubMed
description SARS-CoV-2 (Severe Acute Respiratory Syndrome coronavirus-2) is the third coronavirus to emerge as a cause of severe and frequently fatal pneumonia epidemics in humans, joining SARS-CoV and MERS-CoV (Middle East Respiratory Syndrome-coronavirus). As with many infectious diseases, the immune response to coronavirus infection may act as a double-edged sword: necessary for promoting antiviral host defense, but, if not appropriately regulated, also able to incite life-threatening immunopathology. Key immunoregulatory mediators include the chemokines, a large family of leukocyte chemoattractants that coordinate leukocyte infiltration, positioning and activation in infected tissue by acting at specific G protein-coupled receptors. Here, we compare the involvement of chemokines and chemokine receptors during infection with the three epidemic coronaviruses and discuss their potential value as biomarkers and targets for therapeutic development.
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spelling pubmed-78901952021-02-19 Chemokine Regulation During Epidemic Coronavirus Infection Majumdar, Shamik Murphy, Philip M. Front Pharmacol Pharmacology SARS-CoV-2 (Severe Acute Respiratory Syndrome coronavirus-2) is the third coronavirus to emerge as a cause of severe and frequently fatal pneumonia epidemics in humans, joining SARS-CoV and MERS-CoV (Middle East Respiratory Syndrome-coronavirus). As with many infectious diseases, the immune response to coronavirus infection may act as a double-edged sword: necessary for promoting antiviral host defense, but, if not appropriately regulated, also able to incite life-threatening immunopathology. Key immunoregulatory mediators include the chemokines, a large family of leukocyte chemoattractants that coordinate leukocyte infiltration, positioning and activation in infected tissue by acting at specific G protein-coupled receptors. Here, we compare the involvement of chemokines and chemokine receptors during infection with the three epidemic coronaviruses and discuss their potential value as biomarkers and targets for therapeutic development. Frontiers Media S.A. 2021-02-04 /pmc/articles/PMC7890195/ /pubmed/33613280 http://dx.doi.org/10.3389/fphar.2020.600369 Text en Copyright © 2021 Majumdar and Murphy. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (http://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Majumdar, Shamik
Murphy, Philip M.
Chemokine Regulation During Epidemic Coronavirus Infection
title Chemokine Regulation During Epidemic Coronavirus Infection
title_full Chemokine Regulation During Epidemic Coronavirus Infection
title_fullStr Chemokine Regulation During Epidemic Coronavirus Infection
title_full_unstemmed Chemokine Regulation During Epidemic Coronavirus Infection
title_short Chemokine Regulation During Epidemic Coronavirus Infection
title_sort chemokine regulation during epidemic coronavirus infection
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890195/
https://www.ncbi.nlm.nih.gov/pubmed/33613280
http://dx.doi.org/10.3389/fphar.2020.600369
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