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COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases
Autoimmune diseases and infections are often closely intertwined. Patients with autoimmune diseases are more susceptible to infections due to either active autoimmune disease or the medications used to treat them. Based on infections as environmental triggers of autoimmunity, an autoimmune response...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870870/ https://www.ncbi.nlm.nih.gov/pubmed/33574819 http://dx.doi.org/10.3389/fimmu.2020.611318 |
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author | Lakota, Katja Perdan-Pirkmajer, Katja Hočevar, Alojzija Sodin-Semrl, Snezna Rotar, Žiga Čučnik, Saša Žigon, Polona |
author_facet | Lakota, Katja Perdan-Pirkmajer, Katja Hočevar, Alojzija Sodin-Semrl, Snezna Rotar, Žiga Čučnik, Saša Žigon, Polona |
author_sort | Lakota, Katja |
collection | PubMed |
description | Autoimmune diseases and infections are often closely intertwined. Patients with autoimmune diseases are more susceptible to infections due to either active autoimmune disease or the medications used to treat them. Based on infections as environmental triggers of autoimmunity, an autoimmune response would also be expected in COVID-19. Although some studies have shown the occurance of autoantibodies and the possible development of autoimmune diseases after SARS-CoV-2 infection, current data suggest that the levels of autoantibodies following SARS-CoV-2 infection is comparable to that of some other known infections and that the autoantibodies might only be transient. The risk of SARS-CoV-2 infection in patients with a systemic autoimmune rheumatic disease (SARD) appears slightly higher compared to the general population and the course of COVID-19 disease does not seem to be very different, however, specific therapies such as glucocorticoids and anti-TNF might modulate the risk of hospitalization/death. Cytokine release syndrome is a severe complication in COVID-19. Many drugs used for the treatment of SARD are directly or indirectly targeting cytokines involved in the cytokine release syndrome, therefore it has been suggested that they could also be effective in COVID-19, but more evidence on the use of these medications for the treatment of COVID-19 is currently being collected. |
format | Online Article Text |
id | pubmed-7870870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78708702021-02-10 COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases Lakota, Katja Perdan-Pirkmajer, Katja Hočevar, Alojzija Sodin-Semrl, Snezna Rotar, Žiga Čučnik, Saša Žigon, Polona Front Immunol Immunology Autoimmune diseases and infections are often closely intertwined. Patients with autoimmune diseases are more susceptible to infections due to either active autoimmune disease or the medications used to treat them. Based on infections as environmental triggers of autoimmunity, an autoimmune response would also be expected in COVID-19. Although some studies have shown the occurance of autoantibodies and the possible development of autoimmune diseases after SARS-CoV-2 infection, current data suggest that the levels of autoantibodies following SARS-CoV-2 infection is comparable to that of some other known infections and that the autoantibodies might only be transient. The risk of SARS-CoV-2 infection in patients with a systemic autoimmune rheumatic disease (SARD) appears slightly higher compared to the general population and the course of COVID-19 disease does not seem to be very different, however, specific therapies such as glucocorticoids and anti-TNF might modulate the risk of hospitalization/death. Cytokine release syndrome is a severe complication in COVID-19. Many drugs used for the treatment of SARD are directly or indirectly targeting cytokines involved in the cytokine release syndrome, therefore it has been suggested that they could also be effective in COVID-19, but more evidence on the use of these medications for the treatment of COVID-19 is currently being collected. Frontiers Media S.A. 2021-01-26 /pmc/articles/PMC7870870/ /pubmed/33574819 http://dx.doi.org/10.3389/fimmu.2020.611318 Text en Copyright © 2021 Lakota, Perdan-Pirkmajer, Hočevar, Sodin-Semrl, Rotar, Čučnik and Žigon http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Lakota, Katja Perdan-Pirkmajer, Katja Hočevar, Alojzija Sodin-Semrl, Snezna Rotar, Žiga Čučnik, Saša Žigon, Polona COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases |
title | COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases |
title_full | COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases |
title_fullStr | COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases |
title_full_unstemmed | COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases |
title_short | COVID-19 in Association With Development, Course, and Treatment of Systemic Autoimmune Rheumatic Diseases |
title_sort | covid-19 in association with development, course, and treatment of systemic autoimmune rheumatic diseases |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870870/ https://www.ncbi.nlm.nih.gov/pubmed/33574819 http://dx.doi.org/10.3389/fimmu.2020.611318 |
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