Cargando…
Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes
COVID-19 is characterized by excessive production of pro-inflammatory cytokines and acute lung damage associated with patient mortality. While multiple inflammatory cytokines are produced by innate immune cells during SARS-CoV-2 infection, we found that only the combination of TNF-α and IFN-γ induce...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674074/ https://www.ncbi.nlm.nih.gov/pubmed/33278357 http://dx.doi.org/10.1016/j.cell.2020.11.025 |
_version_ | 1783611441082793984 |
---|---|
author | Karki, Rajendra Sharma, Bhesh Raj Tuladhar, Shraddha Williams, Evan Peter Zalduondo, Lillian Samir, Parimal Zheng, Min Sundaram, Balamurugan Banoth, Balaji Malireddi, R.K. Subbarao Schreiner, Patrick Neale, Geoffrey Vogel, Peter Webby, Richard Jonsson, Colleen Beth Kanneganti, Thirumala-Devi |
author_facet | Karki, Rajendra Sharma, Bhesh Raj Tuladhar, Shraddha Williams, Evan Peter Zalduondo, Lillian Samir, Parimal Zheng, Min Sundaram, Balamurugan Banoth, Balaji Malireddi, R.K. Subbarao Schreiner, Patrick Neale, Geoffrey Vogel, Peter Webby, Richard Jonsson, Colleen Beth Kanneganti, Thirumala-Devi |
author_sort | Karki, Rajendra |
collection | PubMed |
description | COVID-19 is characterized by excessive production of pro-inflammatory cytokines and acute lung damage associated with patient mortality. While multiple inflammatory cytokines are produced by innate immune cells during SARS-CoV-2 infection, we found that only the combination of TNF-α and IFN-γ induced inflammatory cell death characterized by inflammatory cell death, PANoptosis. Mechanistically, TNF-α and IFN-γ co-treatment activated the JAK/STAT1/IRF1 axis, inducing nitric oxide production and driving caspase-8/FADD-mediated PANoptosis. TNF-α and IFN-γ caused a lethal cytokine shock in mice that mirrors the tissue damage and inflammation of COVID-19, and inhibiting PANoptosis protected mice from this pathology and death. Furthermore, treating with neutralizing antibodies against TNF-α and IFN-γ protected mice from mortality during SARS-CoV-2 infection, sepsis, hemophagocytic lymphohistiocytosis, and cytokine shock. Collectively, our findings suggest that blocking the cytokine-mediated inflammatory cell death signaling pathway identified here may benefit patients with COVID-19 or other infectious and autoinflammatory diseases by limiting tissue damage/inflammation. |
format | Online Article Text |
id | pubmed-7674074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76740742020-11-19 Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes Karki, Rajendra Sharma, Bhesh Raj Tuladhar, Shraddha Williams, Evan Peter Zalduondo, Lillian Samir, Parimal Zheng, Min Sundaram, Balamurugan Banoth, Balaji Malireddi, R.K. Subbarao Schreiner, Patrick Neale, Geoffrey Vogel, Peter Webby, Richard Jonsson, Colleen Beth Kanneganti, Thirumala-Devi Cell Article COVID-19 is characterized by excessive production of pro-inflammatory cytokines and acute lung damage associated with patient mortality. While multiple inflammatory cytokines are produced by innate immune cells during SARS-CoV-2 infection, we found that only the combination of TNF-α and IFN-γ induced inflammatory cell death characterized by inflammatory cell death, PANoptosis. Mechanistically, TNF-α and IFN-γ co-treatment activated the JAK/STAT1/IRF1 axis, inducing nitric oxide production and driving caspase-8/FADD-mediated PANoptosis. TNF-α and IFN-γ caused a lethal cytokine shock in mice that mirrors the tissue damage and inflammation of COVID-19, and inhibiting PANoptosis protected mice from this pathology and death. Furthermore, treating with neutralizing antibodies against TNF-α and IFN-γ protected mice from mortality during SARS-CoV-2 infection, sepsis, hemophagocytic lymphohistiocytosis, and cytokine shock. Collectively, our findings suggest that blocking the cytokine-mediated inflammatory cell death signaling pathway identified here may benefit patients with COVID-19 or other infectious and autoinflammatory diseases by limiting tissue damage/inflammation. Elsevier Inc. 2021-01-07 2020-11-19 /pmc/articles/PMC7674074/ /pubmed/33278357 http://dx.doi.org/10.1016/j.cell.2020.11.025 Text en © 2020 Elsevier Inc. 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 Karki, Rajendra Sharma, Bhesh Raj Tuladhar, Shraddha Williams, Evan Peter Zalduondo, Lillian Samir, Parimal Zheng, Min Sundaram, Balamurugan Banoth, Balaji Malireddi, R.K. Subbarao Schreiner, Patrick Neale, Geoffrey Vogel, Peter Webby, Richard Jonsson, Colleen Beth Kanneganti, Thirumala-Devi Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes |
title | Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes |
title_full | Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes |
title_fullStr | Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes |
title_full_unstemmed | Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes |
title_short | Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes |
title_sort | synergism of tnf-α and ifn-γ triggers inflammatory cell death, tissue damage, and mortality in sars-cov-2 infection and cytokine shock syndromes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674074/ https://www.ncbi.nlm.nih.gov/pubmed/33278357 http://dx.doi.org/10.1016/j.cell.2020.11.025 |
work_keys_str_mv | AT karkirajendra synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT sharmabheshraj synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT tuladharshraddha synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT williamsevanpeter synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT zalduondolillian synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT samirparimal synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT zhengmin synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT sundarambalamurugan synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT banothbalaji synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT malireddirksubbarao synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT schreinerpatrick synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT nealegeoffrey synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT vogelpeter synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT webbyrichard synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT jonssoncolleenbeth synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes AT kannegantithirumaladevi synergismoftnfaandifngtriggersinflammatorycelldeathtissuedamageandmortalityinsarscov2infectionandcytokineshocksyndromes |