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S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes
Coronavirus disease 2019 (COVID-19) has a broad range of clinical manifestations, highlighting the need for specific diagnostic tools to predict disease severity and improve patient prognosis. Recently, calprotectin (S100A8/A9) has been proposed as a potential biomarker for COVID-19, as elevated ser...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520505/ https://www.ncbi.nlm.nih.gov/pubmed/34728150 http://dx.doi.org/10.1016/j.cytogfr.2021.10.004 |
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author | Mellett, Leah Khader, Shabaana A. |
author_facet | Mellett, Leah Khader, Shabaana A. |
author_sort | Mellett, Leah |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) has a broad range of clinical manifestations, highlighting the need for specific diagnostic tools to predict disease severity and improve patient prognosis. Recently, calprotectin (S100A8/A9) has been proposed as a potential biomarker for COVID-19, as elevated serum S100A8/A9 levels are associated with critical COVID-19 cases and can distinguish between mild and severe disease states. S100A8/A9 is an alarmin that mediates host proinflammatory responses during infection and it has been postulated that S100A8/A9 modulates the cytokine storm; the hallmark of fatal COVID-19 cases. However, it has yet to be determined if S100A8/A9 is a bona-fide biomarker for COVID-19. S100A8/A9 is widely implicated in a variety of inflammatory conditions, such as cystic fibrosis (CF) and chronic obstructive pulmonary disorder (COPD), as well as pulmonary infectious diseases, including tuberculosis and influenza. Therefore, understanding how S100A8/A9 levels correlate with immune responses during inflammatory diseases is necessary to evaluate its candidacy as a potential COVID-19 biomarker. This review will outline the protective and detrimental roles of S100A8/A9 during infection, summarize the recent findings detailing the contributions of S100A8/A9 to COVID-19 pathogenesis, and highlight its potential as diagnostic biomarker and a therapeutic target for pulmonary infectious diseases, including COVID-19. |
format | Online Article Text |
id | pubmed-8520505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85205052021-10-18 S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes Mellett, Leah Khader, Shabaana A. Cytokine Growth Factor Rev Article Coronavirus disease 2019 (COVID-19) has a broad range of clinical manifestations, highlighting the need for specific diagnostic tools to predict disease severity and improve patient prognosis. Recently, calprotectin (S100A8/A9) has been proposed as a potential biomarker for COVID-19, as elevated serum S100A8/A9 levels are associated with critical COVID-19 cases and can distinguish between mild and severe disease states. S100A8/A9 is an alarmin that mediates host proinflammatory responses during infection and it has been postulated that S100A8/A9 modulates the cytokine storm; the hallmark of fatal COVID-19 cases. However, it has yet to be determined if S100A8/A9 is a bona-fide biomarker for COVID-19. S100A8/A9 is widely implicated in a variety of inflammatory conditions, such as cystic fibrosis (CF) and chronic obstructive pulmonary disorder (COPD), as well as pulmonary infectious diseases, including tuberculosis and influenza. Therefore, understanding how S100A8/A9 levels correlate with immune responses during inflammatory diseases is necessary to evaluate its candidacy as a potential COVID-19 biomarker. This review will outline the protective and detrimental roles of S100A8/A9 during infection, summarize the recent findings detailing the contributions of S100A8/A9 to COVID-19 pathogenesis, and highlight its potential as diagnostic biomarker and a therapeutic target for pulmonary infectious diseases, including COVID-19. Elsevier Ltd. 2022-02 2021-10-17 /pmc/articles/PMC8520505/ /pubmed/34728150 http://dx.doi.org/10.1016/j.cytogfr.2021.10.004 Text en © 2021 Elsevier Ltd. All rights reserved. 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 Mellett, Leah Khader, Shabaana A. S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes |
title | S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes |
title_full | S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes |
title_fullStr | S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes |
title_full_unstemmed | S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes |
title_short | S100A8/A9 in COVID-19 pathogenesis: Impact on clinical outcomes |
title_sort | s100a8/a9 in covid-19 pathogenesis: impact on clinical outcomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520505/ https://www.ncbi.nlm.nih.gov/pubmed/34728150 http://dx.doi.org/10.1016/j.cytogfr.2021.10.004 |
work_keys_str_mv | AT mellettleah s100a8a9incovid19pathogenesisimpactonclinicaloutcomes AT khadershabaanaa s100a8a9incovid19pathogenesisimpactonclinicaloutcomes |