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Adaptive Immunity and the Risk of Autoreactivity in COVID-19

While first and foremost considered a respiratory infection, COVID-19 can result in complications affecting multiple organs. Immune responses in COVID-19 can both protect against the disease as well as drive it. Insights into these responses, and specifically the targets being recognised by the immu...

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Autores principales: Moody, Rhiane, Wilson, Kirsty, Flanagan, Katie L., Jaworowski, Anthony, Plebanski, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396528/
https://www.ncbi.nlm.nih.gov/pubmed/34445670
http://dx.doi.org/10.3390/ijms22168965
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author Moody, Rhiane
Wilson, Kirsty
Flanagan, Katie L.
Jaworowski, Anthony
Plebanski, Magdalena
author_facet Moody, Rhiane
Wilson, Kirsty
Flanagan, Katie L.
Jaworowski, Anthony
Plebanski, Magdalena
author_sort Moody, Rhiane
collection PubMed
description While first and foremost considered a respiratory infection, COVID-19 can result in complications affecting multiple organs. Immune responses in COVID-19 can both protect against the disease as well as drive it. Insights into these responses, and specifically the targets being recognised by the immune system, are of vital importance in understanding the side effects of COVID-19 and associated pathologies. The body’s adaptive immunity recognises and responds against specific targets (antigens) expressed by foreign pathogens, but not usually to target self-antigens. However, if the immune system becomes dysfunctional, adaptive immune cells can react to self-antigens, which can result in autoimmune disease. Viral infections are well reported to be associated with, or exacerbate, autoimmune diseases such as multiple sclerosis (MS) and systemic lupus erythematosus (SLE). In COVID-19 patients, both new onset MS and SLE, as well as the occurrence of other autoimmune-like pathologies, have been reported. Additionally, the presence of autoantibodies, both with and without known associations to autoimmune diseases, have been found. Herein we describe the mechanisms of virally induced autoimmunity and summarise some of the emerging reports on the autoimmune-like diseases and autoreactivity that is reported to be associated with SARS-CoV-2 infection.
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spelling pubmed-83965282021-08-28 Adaptive Immunity and the Risk of Autoreactivity in COVID-19 Moody, Rhiane Wilson, Kirsty Flanagan, Katie L. Jaworowski, Anthony Plebanski, Magdalena Int J Mol Sci Review While first and foremost considered a respiratory infection, COVID-19 can result in complications affecting multiple organs. Immune responses in COVID-19 can both protect against the disease as well as drive it. Insights into these responses, and specifically the targets being recognised by the immune system, are of vital importance in understanding the side effects of COVID-19 and associated pathologies. The body’s adaptive immunity recognises and responds against specific targets (antigens) expressed by foreign pathogens, but not usually to target self-antigens. However, if the immune system becomes dysfunctional, adaptive immune cells can react to self-antigens, which can result in autoimmune disease. Viral infections are well reported to be associated with, or exacerbate, autoimmune diseases such as multiple sclerosis (MS) and systemic lupus erythematosus (SLE). In COVID-19 patients, both new onset MS and SLE, as well as the occurrence of other autoimmune-like pathologies, have been reported. Additionally, the presence of autoantibodies, both with and without known associations to autoimmune diseases, have been found. Herein we describe the mechanisms of virally induced autoimmunity and summarise some of the emerging reports on the autoimmune-like diseases and autoreactivity that is reported to be associated with SARS-CoV-2 infection. MDPI 2021-08-20 /pmc/articles/PMC8396528/ /pubmed/34445670 http://dx.doi.org/10.3390/ijms22168965 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Moody, Rhiane
Wilson, Kirsty
Flanagan, Katie L.
Jaworowski, Anthony
Plebanski, Magdalena
Adaptive Immunity and the Risk of Autoreactivity in COVID-19
title Adaptive Immunity and the Risk of Autoreactivity in COVID-19
title_full Adaptive Immunity and the Risk of Autoreactivity in COVID-19
title_fullStr Adaptive Immunity and the Risk of Autoreactivity in COVID-19
title_full_unstemmed Adaptive Immunity and the Risk of Autoreactivity in COVID-19
title_short Adaptive Immunity and the Risk of Autoreactivity in COVID-19
title_sort adaptive immunity and the risk of autoreactivity in covid-19
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396528/
https://www.ncbi.nlm.nih.gov/pubmed/34445670
http://dx.doi.org/10.3390/ijms22168965
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