(2021) Contribution of STAT3 to the pathogenesis of COVID-19. Microb Pathog. p. 104836. ISSN 0882-4010 (Print) 0882-4010
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Abstract
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.
Item Type: | Article |
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Keywords: | Keywords: COVID-19; Immune response; Inflammation; Pathogenesis; SARS-CoV-2; STAT3; Treatment. |
Subjects: | WC Communicable Diseases > WC 500-590 Virus Diseases |
Divisions: | Research Vice-Chancellor Department > Immunology of Infectious Diseases Research Center |
Page Range: | p. 104836 |
Journal or Publication Title: | Microb Pathog |
Journal Index: | Pubmed, Scopus |
Volume: | 154 |
Publisher: | Elsevier B.V., All rights reserved. |
Identification Number: | https://doi.org/10.1016/j.micpath.2021.104836 |
ISSN: | 0882-4010 (Print) 0882-4010 |
Depositing User: | خانم مهتاب اکبری |
URI: | http://eprints.rums.ac.ir/id/eprint/28784 |
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