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Contribution of STAT3 to the pathogenesis of COVID-19
Hyper-inflammatory responses, lymphopenia, unbalanced immune responses, cytokine storm, large viral replication and massive cell death play fundamental roles in the pathogenesis of COVID-19. Extreme production of many kinds of pro-inflammatory cytokines and chemokines occur in severe COVID-19 that c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937040/ https://www.ncbi.nlm.nih.gov/pubmed/33691172 http://dx.doi.org/10.1016/j.micpath.2021.104836 |
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author | Jafarzadeh, Abdollah Nemati, Maryam Jafarzadeh, Sara |
author_facet | Jafarzadeh, Abdollah Nemati, Maryam Jafarzadeh, Sara |
author_sort | Jafarzadeh, Abdollah |
collection | PubMed |
description | Hyper-inflammatory responses, lymphopenia, unbalanced immune responses, cytokine storm, large viral replication and massive cell death play fundamental roles in the pathogenesis of COVID-19. Extreme production of many kinds of pro-inflammatory cytokines and chemokines occur in severe COVID-19 that called cytokine storm. Signal transducer and activator of transcription-3 (STAT-3) present in the cytoplasm in an inactive form and can be stimulated by a vast range of cytokines, chemokines and growth factors. Thus, STAT-3 can participate in the induction of inflammatory responses during coronavirus infections. STAT-3 can also suppress anti-virus interferon response and induce unbalanced anti-virus adaptive immune response, through influencing Th17-, Th1-, Treg-, and B cell-mediated functions. Furthermore, STAT-3 can contribute to the M2 macrophage polarization, lung fibrosis and thrombosis. Moreover, STAT-3 may be directly targeted by some virus-derived protein and operate as a pro-viral or anti-viral element in a virus-specific process. Here, the possible contribution of STAT-3 to the pathogenesis of COVID-19 was explained, while providing potential approaches to target this transcription factor in an attempt for COVID-19 treatment. |
format | Online Article Text |
id | pubmed-7937040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79370402021-03-08 Contribution of STAT3 to the pathogenesis of COVID-19 Jafarzadeh, Abdollah Nemati, Maryam Jafarzadeh, Sara Microb Pathog Article Hyper-inflammatory responses, lymphopenia, unbalanced immune responses, cytokine storm, large viral replication and massive cell death play fundamental roles in the pathogenesis of COVID-19. Extreme production of many kinds of pro-inflammatory cytokines and chemokines occur in severe COVID-19 that called cytokine storm. Signal transducer and activator of transcription-3 (STAT-3) present in the cytoplasm in an inactive form and can be stimulated by a vast range of cytokines, chemokines and growth factors. Thus, STAT-3 can participate in the induction of inflammatory responses during coronavirus infections. STAT-3 can also suppress anti-virus interferon response and induce unbalanced anti-virus adaptive immune response, through influencing Th17-, Th1-, Treg-, and B cell-mediated functions. Furthermore, STAT-3 can contribute to the M2 macrophage polarization, lung fibrosis and thrombosis. Moreover, STAT-3 may be directly targeted by some virus-derived protein and operate as a pro-viral or anti-viral element in a virus-specific process. Here, the possible contribution of STAT-3 to the pathogenesis of COVID-19 was explained, while providing potential approaches to target this transcription factor in an attempt for COVID-19 treatment. Elsevier Ltd. 2021-05 2021-03-07 /pmc/articles/PMC7937040/ /pubmed/33691172 http://dx.doi.org/10.1016/j.micpath.2021.104836 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 Jafarzadeh, Abdollah Nemati, Maryam Jafarzadeh, Sara Contribution of STAT3 to the pathogenesis of COVID-19 |
title | Contribution of STAT3 to the pathogenesis of COVID-19 |
title_full | Contribution of STAT3 to the pathogenesis of COVID-19 |
title_fullStr | Contribution of STAT3 to the pathogenesis of COVID-19 |
title_full_unstemmed | Contribution of STAT3 to the pathogenesis of COVID-19 |
title_short | Contribution of STAT3 to the pathogenesis of COVID-19 |
title_sort | contribution of stat3 to the pathogenesis of covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937040/ https://www.ncbi.nlm.nih.gov/pubmed/33691172 http://dx.doi.org/10.1016/j.micpath.2021.104836 |
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