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Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review
BACKGROUND: Influenza virus (IV) is a leading cause of respiratory tract infections, eliciting responses from key innate immune cells such as Macrophages (MQs), Neutrophils, and Dendritic Cells (DCs). These cells employ diverse mechanisms to combat IV, with Inflammasomes playing a pivotal role in vi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521376/ https://www.ncbi.nlm.nih.gov/pubmed/37773712 http://dx.doi.org/10.1002/iid3.997 |
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author | Wei, Li Wang, Xufang Zhou, Huifei |
author_facet | Wei, Li Wang, Xufang Zhou, Huifei |
author_sort | Wei, Li |
collection | PubMed |
description | BACKGROUND: Influenza virus (IV) is a leading cause of respiratory tract infections, eliciting responses from key innate immune cells such as Macrophages (MQs), Neutrophils, and Dendritic Cells (DCs). These cells employ diverse mechanisms to combat IV, with Inflammasomes playing a pivotal role in viral infection control. Cellular death mechanisms, including Pyroptosis, Apoptosis, and Necroptosis (collectively called PANoptosis), significantly contribute to the innate immune response. METHODS: In this updated review, we delve into the intricate relationship between PANoptosis and Inflammasomes within innate immune cells (MQs, Neutrophils, and DCs) during IV infections. We explore the strategies employed by IV to evade these immune defenses and the consequences of unchecked PANoptosis and inflammasome activation, including the potential development of severe complications such as cytokine storms and tissue damage. RESULTS: Our analysis underscores the interplay between PANoptosis and Inflammasomes as a critical aspect of the innate immune response against IV. We provide insights into IV's various mechanisms to subvert these immune pathways and highlight the importance of understanding these interactions to develop effective antiviral medications. CONCLUSION: A comprehensive understanding of the dynamic interactions between PANoptosis, Inflammasomes, and IV is essential for advancing our knowledge of innate immune responses to viral infections. This knowledge will be invaluable in developing targeted antiviral therapies to combat IV and mitigate potential complications, including cytokine storms and tissue damage. |
format | Online Article Text |
id | pubmed-10521376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105213762023-09-27 Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review Wei, Li Wang, Xufang Zhou, Huifei Immun Inflamm Dis Review Article BACKGROUND: Influenza virus (IV) is a leading cause of respiratory tract infections, eliciting responses from key innate immune cells such as Macrophages (MQs), Neutrophils, and Dendritic Cells (DCs). These cells employ diverse mechanisms to combat IV, with Inflammasomes playing a pivotal role in viral infection control. Cellular death mechanisms, including Pyroptosis, Apoptosis, and Necroptosis (collectively called PANoptosis), significantly contribute to the innate immune response. METHODS: In this updated review, we delve into the intricate relationship between PANoptosis and Inflammasomes within innate immune cells (MQs, Neutrophils, and DCs) during IV infections. We explore the strategies employed by IV to evade these immune defenses and the consequences of unchecked PANoptosis and inflammasome activation, including the potential development of severe complications such as cytokine storms and tissue damage. RESULTS: Our analysis underscores the interplay between PANoptosis and Inflammasomes as a critical aspect of the innate immune response against IV. We provide insights into IV's various mechanisms to subvert these immune pathways and highlight the importance of understanding these interactions to develop effective antiviral medications. CONCLUSION: A comprehensive understanding of the dynamic interactions between PANoptosis, Inflammasomes, and IV is essential for advancing our knowledge of innate immune responses to viral infections. This knowledge will be invaluable in developing targeted antiviral therapies to combat IV and mitigate potential complications, including cytokine storms and tissue damage. John Wiley and Sons Inc. 2023-09-26 /pmc/articles/PMC10521376/ /pubmed/37773712 http://dx.doi.org/10.1002/iid3.997 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Wei, Li Wang, Xufang Zhou, Huifei Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review |
title | Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review |
title_full | Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review |
title_fullStr | Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review |
title_full_unstemmed | Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review |
title_short | Interaction among inflammasome, PANoptosise, and innate immune cells in infection of influenza virus: Updated review |
title_sort | interaction among inflammasome, panoptosise, and innate immune cells in infection of influenza virus: updated review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521376/ https://www.ncbi.nlm.nih.gov/pubmed/37773712 http://dx.doi.org/10.1002/iid3.997 |
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