Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783526685913645056 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7185015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT felsensteinsusanna covid19immunologyandtreatmentoptions AT herbertjennya covid19immunologyandtreatmentoptions AT mcnamarapauls covid19immunologyandtreatmentoptions AT hedrichchristianm covid19immunologyandtreatmentoptions |