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Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection

BACKGROUND: The presentation of peptides and the subsequent immune response depend on the MHC characteristics and influence the specificity of the immune response. Several studies have found an association between HLA variants and differential COVID-19 outcomes and have shown that HLA genotypes are...

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Autores principales: Fischer, Johannes C., Balz, Vera, Jazmati, Danny, Bölke, Edwin, Freise, Noemi F., Keitel, Verena, Feldt, Torsten, Jensen, Björn-Erik Ole, Bode, Johannes, Lüdde, Tom, Häussinger, Dieter, Adams, Ortwin, Schneider, E. Marion, Enczmann, Jürgen, Rox, Jutta M., Hermsen, Derik, Schulze-Bosse, Karin, Kindgen-Milles, Detlef, Knoefel, Wolfram Trudo, van Griensven, Martijn, Haussmann, Jan, Tamaskovics, Balint, Plettenberg, Christian, Scheckenbach, Kathrin, Corradini, Stefanie, Pedoto, Alessia, Maas, Kitti, Schmidt, Livia, Grebe, Olaf, Esposito, Irene, Ehrhardt, Anja, Peiper, Matthias, Buhren, Bettina Alexandra, Calles, Christian, Stöhr, Andreas, Gerber, Peter Arne, Lichtenberg, Artur, Schelzig, Hubert, Flaig, Yechan, Rezazadeh, Amir, Budach, Wilfried, Matuschek, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676819/
https://www.ncbi.nlm.nih.gov/pubmed/36411478
http://dx.doi.org/10.1186/s40001-022-00864-z
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author Fischer, Johannes C.
Balz, Vera
Jazmati, Danny
Bölke, Edwin
Freise, Noemi F.
Keitel, Verena
Feldt, Torsten
Jensen, Björn-Erik Ole
Bode, Johannes
Lüdde, Tom
Häussinger, Dieter
Adams, Ortwin
Schneider, E. Marion
Enczmann, Jürgen
Rox, Jutta M.
Hermsen, Derik
Schulze-Bosse, Karin
Kindgen-Milles, Detlef
Knoefel, Wolfram Trudo
van Griensven, Martijn
Haussmann, Jan
Tamaskovics, Balint
Plettenberg, Christian
Scheckenbach, Kathrin
Corradini, Stefanie
Pedoto, Alessia
Maas, Kitti
Schmidt, Livia
Grebe, Olaf
Esposito, Irene
Ehrhardt, Anja
Peiper, Matthias
Buhren, Bettina Alexandra
Calles, Christian
Stöhr, Andreas
Gerber, Peter Arne
Lichtenberg, Artur
Schelzig, Hubert
Flaig, Yechan
Rezazadeh, Amir
Budach, Wilfried
Matuschek, Christiane
author_facet Fischer, Johannes C.
Balz, Vera
Jazmati, Danny
Bölke, Edwin
Freise, Noemi F.
Keitel, Verena
Feldt, Torsten
Jensen, Björn-Erik Ole
Bode, Johannes
Lüdde, Tom
Häussinger, Dieter
Adams, Ortwin
Schneider, E. Marion
Enczmann, Jürgen
Rox, Jutta M.
Hermsen, Derik
Schulze-Bosse, Karin
Kindgen-Milles, Detlef
Knoefel, Wolfram Trudo
van Griensven, Martijn
Haussmann, Jan
Tamaskovics, Balint
Plettenberg, Christian
Scheckenbach, Kathrin
Corradini, Stefanie
Pedoto, Alessia
Maas, Kitti
Schmidt, Livia
Grebe, Olaf
Esposito, Irene
Ehrhardt, Anja
Peiper, Matthias
Buhren, Bettina Alexandra
Calles, Christian
Stöhr, Andreas
Gerber, Peter Arne
Lichtenberg, Artur
Schelzig, Hubert
Flaig, Yechan
Rezazadeh, Amir
Budach, Wilfried
Matuschek, Christiane
author_sort Fischer, Johannes C.
collection PubMed
description BACKGROUND: The presentation of peptides and the subsequent immune response depend on the MHC characteristics and influence the specificity of the immune response. Several studies have found an association between HLA variants and differential COVID-19 outcomes and have shown that HLA genotypes are associated with differential immune responses against SARS-CoV-2, particularly in severely ill patients. Information, whether HLA haplotypes are associated with the severity or length of the disease in moderately diseased individuals is absent. METHODS: Next-generation sequencing-based HLA typing was performed in 303 female and 231 male non-hospitalized North Rhine Westphalian patients infected with SARS-CoV2 during the first and second wave. For HLA-Class I, we obtained results from 528 patients, and for HLA-Class II from 531. In those patients, who became ill between March 2020 and January 2021, the 22 most common HLA-Class I (HLA-A, -B, -C) or HLA-Class II (HLA –DRB1/3/4, -DQA1, -DQB1) haplotypes were determined. The identified HLA haplotypes as well as the presence of a CCR5Δ32 mutation and number of O and A blood group alleles were associated to disease severity and duration of the disease. RESULTS: The influence of the HLA haplotypes on disease severity and duration was more pronounced than the influence of age, sex, or ABO blood group. These associations were sex dependent. The presence of mutated CCR5 resulted in a longer recovery period in males. CONCLUSION: The existence of certain HLA haplotypes is associated with more severe disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-022-00864-z.
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spelling pubmed-96768192022-11-21 Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection Fischer, Johannes C. Balz, Vera Jazmati, Danny Bölke, Edwin Freise, Noemi F. Keitel, Verena Feldt, Torsten Jensen, Björn-Erik Ole Bode, Johannes Lüdde, Tom Häussinger, Dieter Adams, Ortwin Schneider, E. Marion Enczmann, Jürgen Rox, Jutta M. Hermsen, Derik Schulze-Bosse, Karin Kindgen-Milles, Detlef Knoefel, Wolfram Trudo van Griensven, Martijn Haussmann, Jan Tamaskovics, Balint Plettenberg, Christian Scheckenbach, Kathrin Corradini, Stefanie Pedoto, Alessia Maas, Kitti Schmidt, Livia Grebe, Olaf Esposito, Irene Ehrhardt, Anja Peiper, Matthias Buhren, Bettina Alexandra Calles, Christian Stöhr, Andreas Gerber, Peter Arne Lichtenberg, Artur Schelzig, Hubert Flaig, Yechan Rezazadeh, Amir Budach, Wilfried Matuschek, Christiane Eur J Med Res Research BACKGROUND: The presentation of peptides and the subsequent immune response depend on the MHC characteristics and influence the specificity of the immune response. Several studies have found an association between HLA variants and differential COVID-19 outcomes and have shown that HLA genotypes are associated with differential immune responses against SARS-CoV-2, particularly in severely ill patients. Information, whether HLA haplotypes are associated with the severity or length of the disease in moderately diseased individuals is absent. METHODS: Next-generation sequencing-based HLA typing was performed in 303 female and 231 male non-hospitalized North Rhine Westphalian patients infected with SARS-CoV2 during the first and second wave. For HLA-Class I, we obtained results from 528 patients, and for HLA-Class II from 531. In those patients, who became ill between March 2020 and January 2021, the 22 most common HLA-Class I (HLA-A, -B, -C) or HLA-Class II (HLA –DRB1/3/4, -DQA1, -DQB1) haplotypes were determined. The identified HLA haplotypes as well as the presence of a CCR5Δ32 mutation and number of O and A blood group alleles were associated to disease severity and duration of the disease. RESULTS: The influence of the HLA haplotypes on disease severity and duration was more pronounced than the influence of age, sex, or ABO blood group. These associations were sex dependent. The presence of mutated CCR5 resulted in a longer recovery period in males. CONCLUSION: The existence of certain HLA haplotypes is associated with more severe disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-022-00864-z. BioMed Central 2022-11-21 /pmc/articles/PMC9676819/ /pubmed/36411478 http://dx.doi.org/10.1186/s40001-022-00864-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Fischer, Johannes C.
Balz, Vera
Jazmati, Danny
Bölke, Edwin
Freise, Noemi F.
Keitel, Verena
Feldt, Torsten
Jensen, Björn-Erik Ole
Bode, Johannes
Lüdde, Tom
Häussinger, Dieter
Adams, Ortwin
Schneider, E. Marion
Enczmann, Jürgen
Rox, Jutta M.
Hermsen, Derik
Schulze-Bosse, Karin
Kindgen-Milles, Detlef
Knoefel, Wolfram Trudo
van Griensven, Martijn
Haussmann, Jan
Tamaskovics, Balint
Plettenberg, Christian
Scheckenbach, Kathrin
Corradini, Stefanie
Pedoto, Alessia
Maas, Kitti
Schmidt, Livia
Grebe, Olaf
Esposito, Irene
Ehrhardt, Anja
Peiper, Matthias
Buhren, Bettina Alexandra
Calles, Christian
Stöhr, Andreas
Gerber, Peter Arne
Lichtenberg, Artur
Schelzig, Hubert
Flaig, Yechan
Rezazadeh, Amir
Budach, Wilfried
Matuschek, Christiane
Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection
title Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection
title_full Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection
title_fullStr Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection
title_full_unstemmed Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection
title_short Prognostic markers for the clinical course in the blood of patients with SARS-CoV-2 infection
title_sort prognostic markers for the clinical course in the blood of patients with sars-cov-2 infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676819/
https://www.ncbi.nlm.nih.gov/pubmed/36411478
http://dx.doi.org/10.1186/s40001-022-00864-z
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