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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...

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Autores principales: Jafarzadeh, Abdollah, Nemati, Maryam, Jafarzadeh, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
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.
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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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