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Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients
BACKGROUND: Increased titers of autoantibodies targeting the G-protein-coupled receptors angiotensin II type 1 receptor (AT1R) and endotelin-1 type A receptor (ETAR) are associated with severe coronavirus disease 2019 (COVID-19) infection. The aim of this study was to determine whether 1) these anti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10446834/ https://www.ncbi.nlm.nih.gov/pubmed/37622126 http://dx.doi.org/10.3389/fimmu.2023.1204433 |
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author | Miedema, Jelle R. Janssen, Matthijs L. von der Thüsen, Jan Endeman, Henrik Langerak, Anton W. Hellemons, Merel E. van Nood, Els Peeters, Bas W. A. Baart, Sara J. Schreurs, Marco W. J. |
author_facet | Miedema, Jelle R. Janssen, Matthijs L. von der Thüsen, Jan Endeman, Henrik Langerak, Anton W. Hellemons, Merel E. van Nood, Els Peeters, Bas W. A. Baart, Sara J. Schreurs, Marco W. J. |
author_sort | Miedema, Jelle R. |
collection | PubMed |
description | BACKGROUND: Increased titers of autoantibodies targeting the G-protein-coupled receptors angiotensin II type 1 receptor (AT1R) and endotelin-1 type A receptor (ETAR) are associated with severe coronavirus disease 2019 (COVID-19) infection. The aim of this study was to determine whether 1) these antibodies are specifically related to COVID-19 disease pathogenesis or increased during any severe respiratory illness, 2) if they are formed during illness, and 3) if they correlate with inflammatory markers or long-term symptoms. METHODS: Antibodies against AT1R, ETAR, and antinuclear antibodies (ANAs) were measured in n=40 prospectively enrolled COVID-19 patients and n=207 COVID-19 patients included in a biobank. Clinical and laboratory findings were prospectively and retrospectively assessed in both cohorts, and results were combined for analysis. The presence of auto-antibodies against AT1R or ETAR in peripheral blood was compared between hospitalized patients with COVID-19 and controls (n=39). Additionally, AT1R and ETAR titers were compared between patients with an unfavorable disease course, defined as intensive care admission and/or death during hospital admission (n=121), to those with a favorable disease course (n=126). A subset of intubated patients with severe COVID-19 were compared to intubated patients with acute respiratory distress syndrome (ARDS) due to any other cause. RESULTS: Significantly increased AT1R and ETAR antibody titers were found in COVID-19 patients compared to controls, while titers were equal between favorable and unfavorable COVID-19 disease course groups. On ICU, intubated patients with COVID-19 had significantly increased AT1R and ETAR titers compared to patients with ARDS due to any other cause. The titers did not correlate with baseline inflammatory markers during admission or with diffusion capacity, cognitive impairment, or fatigue measured at 3 months follow-up. CONCLUSIONS: In patients hospitalized for COVID-19, antibodies against AT1R and ETAR are increased compared to controls and patients with ARDS due to other causes than COVID-19. The baseline antibody titers do not correlate with inflammatory markers or long-term symptoms in this study. |
format | Online Article Text |
id | pubmed-10446834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104468342023-08-24 Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients Miedema, Jelle R. Janssen, Matthijs L. von der Thüsen, Jan Endeman, Henrik Langerak, Anton W. Hellemons, Merel E. van Nood, Els Peeters, Bas W. A. Baart, Sara J. Schreurs, Marco W. J. Front Immunol Immunology BACKGROUND: Increased titers of autoantibodies targeting the G-protein-coupled receptors angiotensin II type 1 receptor (AT1R) and endotelin-1 type A receptor (ETAR) are associated with severe coronavirus disease 2019 (COVID-19) infection. The aim of this study was to determine whether 1) these antibodies are specifically related to COVID-19 disease pathogenesis or increased during any severe respiratory illness, 2) if they are formed during illness, and 3) if they correlate with inflammatory markers or long-term symptoms. METHODS: Antibodies against AT1R, ETAR, and antinuclear antibodies (ANAs) were measured in n=40 prospectively enrolled COVID-19 patients and n=207 COVID-19 patients included in a biobank. Clinical and laboratory findings were prospectively and retrospectively assessed in both cohorts, and results were combined for analysis. The presence of auto-antibodies against AT1R or ETAR in peripheral blood was compared between hospitalized patients with COVID-19 and controls (n=39). Additionally, AT1R and ETAR titers were compared between patients with an unfavorable disease course, defined as intensive care admission and/or death during hospital admission (n=121), to those with a favorable disease course (n=126). A subset of intubated patients with severe COVID-19 were compared to intubated patients with acute respiratory distress syndrome (ARDS) due to any other cause. RESULTS: Significantly increased AT1R and ETAR antibody titers were found in COVID-19 patients compared to controls, while titers were equal between favorable and unfavorable COVID-19 disease course groups. On ICU, intubated patients with COVID-19 had significantly increased AT1R and ETAR titers compared to patients with ARDS due to any other cause. The titers did not correlate with baseline inflammatory markers during admission or with diffusion capacity, cognitive impairment, or fatigue measured at 3 months follow-up. CONCLUSIONS: In patients hospitalized for COVID-19, antibodies against AT1R and ETAR are increased compared to controls and patients with ARDS due to other causes than COVID-19. The baseline antibody titers do not correlate with inflammatory markers or long-term symptoms in this study. Frontiers Media S.A. 2023-08-08 /pmc/articles/PMC10446834/ /pubmed/37622126 http://dx.doi.org/10.3389/fimmu.2023.1204433 Text en Copyright © 2023 Miedema, Janssen, Thüsen, Endeman, Langerak, Hellemons, van Nood, Peeters, Baart and Schreurs https://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 Miedema, Jelle R. Janssen, Matthijs L. von der Thüsen, Jan Endeman, Henrik Langerak, Anton W. Hellemons, Merel E. van Nood, Els Peeters, Bas W. A. Baart, Sara J. Schreurs, Marco W. J. Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients |
title | Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients |
title_full | Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients |
title_fullStr | Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients |
title_full_unstemmed | Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients |
title_short | Antibodies against angiotensin II receptor type 1 and endothelin A receptor are increased in COVID-19 patients |
title_sort | antibodies against angiotensin ii receptor type 1 and endothelin a receptor are increased in covid-19 patients |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10446834/ https://www.ncbi.nlm.nih.gov/pubmed/37622126 http://dx.doi.org/10.3389/fimmu.2023.1204433 |
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