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Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease
OBJECTIVE: The development of sufficient COVID-19 vaccines has been a big breakthrough in fighting the global SARS-CoV-2 pandemic. However, vaccination effectiveness can be reduced in patients with autoimmune rheumatic diseases (AIRD). The aim of this study was to identify factors that lead to a dim...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729845/ https://www.ncbi.nlm.nih.gov/pubmed/36597977 http://dx.doi.org/10.1136/rmdopen-2022-002650 |
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author | Frommert, Leonie Maria Arumahandi de Silva, Amanthi Nadira Zernicke, Jan Scholz, Veronika Braun, Tanja Jeworowski, Lara Maria Schwarz, Tatjana Tober-Lau, Pinkus ten Hagen, Alexander Habermann, Elisa Kurth, Florian Sander, Leif Erik Corman, Victor Max Burmester, Gerd-Rüdiger Biesen, Robert Albach, Fredrik N. Klotsche, Jens |
author_facet | Frommert, Leonie Maria Arumahandi de Silva, Amanthi Nadira Zernicke, Jan Scholz, Veronika Braun, Tanja Jeworowski, Lara Maria Schwarz, Tatjana Tober-Lau, Pinkus ten Hagen, Alexander Habermann, Elisa Kurth, Florian Sander, Leif Erik Corman, Victor Max Burmester, Gerd-Rüdiger Biesen, Robert Albach, Fredrik N. Klotsche, Jens |
author_sort | Frommert, Leonie Maria |
collection | PubMed |
description | OBJECTIVE: The development of sufficient COVID-19 vaccines has been a big breakthrough in fighting the global SARS-CoV-2 pandemic. However, vaccination effectiveness can be reduced in patients with autoimmune rheumatic diseases (AIRD). The aim of this study was to identify factors that lead to a diminished humoral vaccination response in patients with AIRD. METHODS: Vaccination response was measured with a surrogate virus neutralisation test and by testing for antibodies directed against the receptor-binding-domain (RBD) of SARS-CoV-2 in 308 fully vaccinated patients with AIRD. In addition, 296 immunocompetent participants were investigated as a control group. Statistical adjusted analysis included covariates with a possible influence on antibody response. RESULTS: Patients with AIRD showed lower antibody responses compared with immunocompetent individuals (median neutralising capacity 90.8% vs 96.5%, p<0.001; median anti-RBD-IgG 5.6 S/CO vs 6.7 S/CO, p<0.001). Lower antibody response was significantly influenced by type of immunosuppressive therapy, but not by rheumatic diagnosis, with patients under rituximab therapy developing the lowest antibody levels. Patients receiving mycophenolate, methotrexate or janus kinase inhibitors also showed reduced vaccination responses. Additional negative influencing factors were vaccination with AZD1222, old age and shorter intervals between the first two vaccinations. CONCLUSION: Certain immunosuppressive therapies are associated with lower antibody responses after vaccination. Additional factors such as vaccine type, age and vaccination interval should be taken into account. We recommend antibody testing in at-risk patients with AIRD and emphasise the importance of booster vaccinations in these patients. |
format | Online Article Text |
id | pubmed-9729845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-97298452022-12-08 Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease Frommert, Leonie Maria Arumahandi de Silva, Amanthi Nadira Zernicke, Jan Scholz, Veronika Braun, Tanja Jeworowski, Lara Maria Schwarz, Tatjana Tober-Lau, Pinkus ten Hagen, Alexander Habermann, Elisa Kurth, Florian Sander, Leif Erik Corman, Victor Max Burmester, Gerd-Rüdiger Biesen, Robert Albach, Fredrik N. Klotsche, Jens RMD Open Epidemiology OBJECTIVE: The development of sufficient COVID-19 vaccines has been a big breakthrough in fighting the global SARS-CoV-2 pandemic. However, vaccination effectiveness can be reduced in patients with autoimmune rheumatic diseases (AIRD). The aim of this study was to identify factors that lead to a diminished humoral vaccination response in patients with AIRD. METHODS: Vaccination response was measured with a surrogate virus neutralisation test and by testing for antibodies directed against the receptor-binding-domain (RBD) of SARS-CoV-2 in 308 fully vaccinated patients with AIRD. In addition, 296 immunocompetent participants were investigated as a control group. Statistical adjusted analysis included covariates with a possible influence on antibody response. RESULTS: Patients with AIRD showed lower antibody responses compared with immunocompetent individuals (median neutralising capacity 90.8% vs 96.5%, p<0.001; median anti-RBD-IgG 5.6 S/CO vs 6.7 S/CO, p<0.001). Lower antibody response was significantly influenced by type of immunosuppressive therapy, but not by rheumatic diagnosis, with patients under rituximab therapy developing the lowest antibody levels. Patients receiving mycophenolate, methotrexate or janus kinase inhibitors also showed reduced vaccination responses. Additional negative influencing factors were vaccination with AZD1222, old age and shorter intervals between the first two vaccinations. CONCLUSION: Certain immunosuppressive therapies are associated with lower antibody responses after vaccination. Additional factors such as vaccine type, age and vaccination interval should be taken into account. We recommend antibody testing in at-risk patients with AIRD and emphasise the importance of booster vaccinations in these patients. BMJ Publishing Group 2022-12-06 /pmc/articles/PMC9729845/ /pubmed/36597977 http://dx.doi.org/10.1136/rmdopen-2022-002650 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Epidemiology Frommert, Leonie Maria Arumahandi de Silva, Amanthi Nadira Zernicke, Jan Scholz, Veronika Braun, Tanja Jeworowski, Lara Maria Schwarz, Tatjana Tober-Lau, Pinkus ten Hagen, Alexander Habermann, Elisa Kurth, Florian Sander, Leif Erik Corman, Victor Max Burmester, Gerd-Rüdiger Biesen, Robert Albach, Fredrik N. Klotsche, Jens Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease |
title | Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease |
title_full | Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease |
title_fullStr | Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease |
title_full_unstemmed | Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease |
title_short | Type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after COVID-19 vaccination in patients with rheumatic disease |
title_sort | type of vaccine and immunosuppressive therapy but not diagnosis critically influence antibody response after covid-19 vaccination in patients with rheumatic disease |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729845/ https://www.ncbi.nlm.nih.gov/pubmed/36597977 http://dx.doi.org/10.1136/rmdopen-2022-002650 |
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