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Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies

The outbreak of coronavirus disease 2019 (COVID-19) is an unprecedented global health crisis. Tissue and peripheral blood analysis indicate profound, aberrant myeloid cell activation, cytokine storm, and lymphopenia, with unknown immunopathological mechanisms. Spatiotemporal control of the quality a...

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Autores principales: Zhou, Ting, Su, Tina Tianjiao, Mudianto, Tenny, Wang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481961/
https://www.ncbi.nlm.nih.gov/pubmed/32910820
http://dx.doi.org/10.1084/jem.20200674
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author Zhou, Ting
Su, Tina Tianjiao
Mudianto, Tenny
Wang, Jun
author_facet Zhou, Ting
Su, Tina Tianjiao
Mudianto, Tenny
Wang, Jun
author_sort Zhou, Ting
collection PubMed
description The outbreak of coronavirus disease 2019 (COVID-19) is an unprecedented global health crisis. Tissue and peripheral blood analysis indicate profound, aberrant myeloid cell activation, cytokine storm, and lymphopenia, with unknown immunopathological mechanisms. Spatiotemporal control of the quality and quantity of the antiviral immune responses involves synchronized cellular and molecular cascades and cross-talk between innate and adaptive immunity. Dysregulated responses in immunity, such as at the stages of immune sensing, alarming, polarization, and resolution, may contribute to disease pathology. Herein, we approach SARS-CoV-2 through an immunomodulatory lens, discussing possible mechanisms of the asynchronized antiviral immune response and proposing potential therapeutic strategies to correct the dysregulation.
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spelling pubmed-74819612020-09-21 Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies Zhou, Ting Su, Tina Tianjiao Mudianto, Tenny Wang, Jun J Exp Med Perspective The outbreak of coronavirus disease 2019 (COVID-19) is an unprecedented global health crisis. Tissue and peripheral blood analysis indicate profound, aberrant myeloid cell activation, cytokine storm, and lymphopenia, with unknown immunopathological mechanisms. Spatiotemporal control of the quality and quantity of the antiviral immune responses involves synchronized cellular and molecular cascades and cross-talk between innate and adaptive immunity. Dysregulated responses in immunity, such as at the stages of immune sensing, alarming, polarization, and resolution, may contribute to disease pathology. Herein, we approach SARS-CoV-2 through an immunomodulatory lens, discussing possible mechanisms of the asynchronized antiviral immune response and proposing potential therapeutic strategies to correct the dysregulation. Rockefeller University Press 2020-09-10 /pmc/articles/PMC7481961/ /pubmed/32910820 http://dx.doi.org/10.1084/jem.20200674 Text en © 2020 Zhou et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Perspective
Zhou, Ting
Su, Tina Tianjiao
Mudianto, Tenny
Wang, Jun
Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies
title Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies
title_full Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies
title_fullStr Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies
title_full_unstemmed Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies
title_short Immune asynchrony in COVID-19 pathogenesis and potential immunotherapies
title_sort immune asynchrony in covid-19 pathogenesis and potential immunotherapies
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481961/
https://www.ncbi.nlm.nih.gov/pubmed/32910820
http://dx.doi.org/10.1084/jem.20200674
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