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Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination
npj Vaccines, Volume: 8, Issue: 1
Swansea University Authors: Ronan Lyons , Gwyneth Davies
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Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.
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DOI (Published version): 10.1038/s41541-023-00614-0
Abstract
Prospective population-based studies investigating associations between reactive symptoms following SARS-CoV-2 vaccination and serologic responses to vaccination are lacking. We therefore conducted a study in 9003 adults from the UK general population receiving SARS-CoV-2 vaccines as part of the nat...
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Springer Science and Business Media LLC
2023
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We therefore conducted a study in 9003 adults from the UK general population receiving SARS-CoV-2 vaccines as part of the national vaccination programme. Titres of combined IgG/IgA/IgM responses to SARS-CoV-2 spike (S) glycoprotein were determined in eluates of dried blood spots collected from all participants before and after vaccination. 4262 (47.3%) participants experienced systemic reactive symptoms after a first vaccine dose. Factors associating with lower risk of such symptoms included older age (aOR per additional 10 years of age 0.85, 95% CI: 0.81–0.90), male vs. female sex (0.59, 0.53–0.65) and receipt of an mRNA vaccine vs. ChAdOx1 nCoV-19 (0.29, 0.26–0.32 for BNT162b2; 0.06, 0.01–0.26 for mRNA-1273). Higher risk of such symptoms was associated with SARS-CoV-2 seropositivity and COVID-19 symptoms prior to vaccination (2.23, 1.78–2.81), but not with SARS-CoV-2 seropositivity in the absence of COVID-19 symptoms (0.94, 0.81–1.09). Presence vs. absence of self-reported anxiety or depression at enrolment associated with higher risk of such symptoms (1.24, 1.12–1.39). Post-vaccination anti-S titres were higher among participants who experienced reactive symptoms after vaccination vs. those who did not (P < 0.001). We conclude that factors influencing risk of systemic symptoms after SARS-CoV-2 vaccination include demographic characteristics, pre-vaccination SARS-CoV-2 serostatus and vaccine type. Participants experiencing reactive symptoms following SARS-CoV-2 vaccination had higher post-vaccination titres of IgG/A/M anti-S antibodies. 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v2 63120 2023-04-12 Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination 83efcf2a9dfcf8b55586999d3d152ac6 0000-0001-5225-000X Ronan Lyons Ronan Lyons true false 92d69cf8519a334ced3f55142c811d95 0000-0003-1218-1008 Gwyneth Davies Gwyneth Davies true false 2023-04-12 HDAT Prospective population-based studies investigating associations between reactive symptoms following SARS-CoV-2 vaccination and serologic responses to vaccination are lacking. We therefore conducted a study in 9003 adults from the UK general population receiving SARS-CoV-2 vaccines as part of the national vaccination programme. Titres of combined IgG/IgA/IgM responses to SARS-CoV-2 spike (S) glycoprotein were determined in eluates of dried blood spots collected from all participants before and after vaccination. 4262 (47.3%) participants experienced systemic reactive symptoms after a first vaccine dose. Factors associating with lower risk of such symptoms included older age (aOR per additional 10 years of age 0.85, 95% CI: 0.81–0.90), male vs. female sex (0.59, 0.53–0.65) and receipt of an mRNA vaccine vs. ChAdOx1 nCoV-19 (0.29, 0.26–0.32 for BNT162b2; 0.06, 0.01–0.26 for mRNA-1273). Higher risk of such symptoms was associated with SARS-CoV-2 seropositivity and COVID-19 symptoms prior to vaccination (2.23, 1.78–2.81), but not with SARS-CoV-2 seropositivity in the absence of COVID-19 symptoms (0.94, 0.81–1.09). Presence vs. absence of self-reported anxiety or depression at enrolment associated with higher risk of such symptoms (1.24, 1.12–1.39). Post-vaccination anti-S titres were higher among participants who experienced reactive symptoms after vaccination vs. those who did not (P < 0.001). We conclude that factors influencing risk of systemic symptoms after SARS-CoV-2 vaccination include demographic characteristics, pre-vaccination SARS-CoV-2 serostatus and vaccine type. Participants experiencing reactive symptoms following SARS-CoV-2 vaccination had higher post-vaccination titres of IgG/A/M anti-S antibodies. Improved public understanding of the frequency of reactogenic symptoms and their positive association with vaccine immunogenicity could potentially increase vaccine uptake. Journal Article npj Vaccines 8 1 Springer Science and Business Media LLC 2059-0105 Fever, Risk factors, RNA vaccines 25 2 2023 2023-02-25 10.1038/s41541-023-00614-0 http://dx.doi.org/10.1038/s41541-023-00614-0 COLLEGE NANME Health Data Science COLLEGE CODE HDAT Swansea University Another institution paid the OA fee Barts Charity 2023-05-18T14:43:29.1034872 2023-04-12T11:11:21.1169491 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Health Data Science Hayley Holt 0000-0003-4153-7982 1 David A. Jolliffe 2 Mohammad Talaei 0000-0002-6901-3665 3 Sian Faustini 4 Giulia Vivaldi 0000-0003-0816-9276 5 Matthew Greenig 6 Alex G. Richter 7 Ronan Lyons 0000-0001-5225-000X 8 Christopher J. Griffiths 9 Frank Kee 10 Aziz Sheikh 11 Gwyneth Davies 0000-0003-1218-1008 12 Seif O. Shaheen 13 Adrian R. Martineau 14 63120__27417__7e333adbbc06445eb5ceb6105a8a79b7.pdf 63120.pdf 2023-05-10T16:12:03.2029285 Output 588628 application/pdf Version of Record true Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. true eng http://creativecommons.org/licenses/by/4.0/ |
title |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination |
spellingShingle |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination Ronan Lyons Gwyneth Davies |
title_short |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination |
title_full |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination |
title_fullStr |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination |
title_full_unstemmed |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination |
title_sort |
Incidence determinants and serological correlates of reactive symptoms following SARS-CoV-2 vaccination |
author_id_str_mv |
83efcf2a9dfcf8b55586999d3d152ac6 92d69cf8519a334ced3f55142c811d95 |
author_id_fullname_str_mv |
83efcf2a9dfcf8b55586999d3d152ac6_***_Ronan Lyons 92d69cf8519a334ced3f55142c811d95_***_Gwyneth Davies |
author |
Ronan Lyons Gwyneth Davies |
author2 |
Hayley Holt David A. Jolliffe Mohammad Talaei Sian Faustini Giulia Vivaldi Matthew Greenig Alex G. Richter Ronan Lyons Christopher J. Griffiths Frank Kee Aziz Sheikh Gwyneth Davies Seif O. Shaheen Adrian R. Martineau |
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10.1038/s41541-023-00614-0 |
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Springer Science and Business Media LLC |
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Prospective population-based studies investigating associations between reactive symptoms following SARS-CoV-2 vaccination and serologic responses to vaccination are lacking. We therefore conducted a study in 9003 adults from the UK general population receiving SARS-CoV-2 vaccines as part of the national vaccination programme. Titres of combined IgG/IgA/IgM responses to SARS-CoV-2 spike (S) glycoprotein were determined in eluates of dried blood spots collected from all participants before and after vaccination. 4262 (47.3%) participants experienced systemic reactive symptoms after a first vaccine dose. Factors associating with lower risk of such symptoms included older age (aOR per additional 10 years of age 0.85, 95% CI: 0.81–0.90), male vs. female sex (0.59, 0.53–0.65) and receipt of an mRNA vaccine vs. ChAdOx1 nCoV-19 (0.29, 0.26–0.32 for BNT162b2; 0.06, 0.01–0.26 for mRNA-1273). Higher risk of such symptoms was associated with SARS-CoV-2 seropositivity and COVID-19 symptoms prior to vaccination (2.23, 1.78–2.81), but not with SARS-CoV-2 seropositivity in the absence of COVID-19 symptoms (0.94, 0.81–1.09). Presence vs. absence of self-reported anxiety or depression at enrolment associated with higher risk of such symptoms (1.24, 1.12–1.39). Post-vaccination anti-S titres were higher among participants who experienced reactive symptoms after vaccination vs. those who did not (P < 0.001). We conclude that factors influencing risk of systemic symptoms after SARS-CoV-2 vaccination include demographic characteristics, pre-vaccination SARS-CoV-2 serostatus and vaccine type. Participants experiencing reactive symptoms following SARS-CoV-2 vaccination had higher post-vaccination titres of IgG/A/M anti-S antibodies. Improved public understanding of the frequency of reactogenic symptoms and their positive association with vaccine immunogenicity could potentially increase vaccine uptake. |
published_date |
2023-02-25T14:43:27Z |
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11.036815 |