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COVID-19: Immunology and treatment options

The novel coronavirus SARS-CoV2 causes COVID-19, a pandemic threatening millions. As protective immunity does not exist in humans and the virus is capable of escaping innate immune responses, it can proliferate, unhindered, in primarily infected tissues. Subsequent cell death results in the release...

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Detalles Bibliográficos
Autores principales: Felsenstein, Susanna, Herbert, Jenny A., McNamara, Paul S., Hedrich, Christian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185015/
https://www.ncbi.nlm.nih.gov/pubmed/32353634
http://dx.doi.org/10.1016/j.clim.2020.108448
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author Felsenstein, Susanna
Herbert, Jenny A.
McNamara, Paul S.
Hedrich, Christian M.
author_facet Felsenstein, Susanna
Herbert, Jenny A.
McNamara, Paul S.
Hedrich, Christian M.
author_sort Felsenstein, Susanna
collection PubMed
description The novel coronavirus SARS-CoV2 causes COVID-19, a pandemic threatening millions. As protective immunity does not exist in humans and the virus is capable of escaping innate immune responses, it can proliferate, unhindered, in primarily infected tissues. Subsequent cell death results in the release of virus particles and intracellular components to the extracellular space, which result in immune cell recruitment, the generation of immune complexes and associated damage. Infection of monocytes/macrophages and/or recruitment of uninfected immune cells can result in massive inflammatory responses later in the disease. Uncontrolled production of pro-inflammatory mediators contributes to ARDS and cytokine storm syndrome. Antiviral agents and immune modulating treatments are currently being trialled. Understanding immune evasion strategies of SARS-CoV2 and the resulting delayed massive immune response will result in the identification of biomarkers that predict outcomes as well as phenotype and disease stage specific treatments that will likely include both antiviral and immune modulating agents.
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spelling pubmed-71850152020-04-27 COVID-19: Immunology and treatment options Felsenstein, Susanna Herbert, Jenny A. McNamara, Paul S. Hedrich, Christian M. Clin Immunol Article The novel coronavirus SARS-CoV2 causes COVID-19, a pandemic threatening millions. As protective immunity does not exist in humans and the virus is capable of escaping innate immune responses, it can proliferate, unhindered, in primarily infected tissues. Subsequent cell death results in the release of virus particles and intracellular components to the extracellular space, which result in immune cell recruitment, the generation of immune complexes and associated damage. Infection of monocytes/macrophages and/or recruitment of uninfected immune cells can result in massive inflammatory responses later in the disease. Uncontrolled production of pro-inflammatory mediators contributes to ARDS and cytokine storm syndrome. Antiviral agents and immune modulating treatments are currently being trialled. Understanding immune evasion strategies of SARS-CoV2 and the resulting delayed massive immune response will result in the identification of biomarkers that predict outcomes as well as phenotype and disease stage specific treatments that will likely include both antiviral and immune modulating agents. Elsevier Inc. 2020-06 2020-04-27 /pmc/articles/PMC7185015/ /pubmed/32353634 http://dx.doi.org/10.1016/j.clim.2020.108448 Text en © 2020 Elsevier Inc. 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
Felsenstein, Susanna
Herbert, Jenny A.
McNamara, Paul S.
Hedrich, Christian M.
COVID-19: Immunology and treatment options
title COVID-19: Immunology and treatment options
title_full COVID-19: Immunology and treatment options
title_fullStr COVID-19: Immunology and treatment options
title_full_unstemmed COVID-19: Immunology and treatment options
title_short COVID-19: Immunology and treatment options
title_sort covid-19: immunology and treatment options
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185015/
https://www.ncbi.nlm.nih.gov/pubmed/32353634
http://dx.doi.org/10.1016/j.clim.2020.108448
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