Leher Gumber
Antibody response to four doses of SARS-CoV-2 vaccine in rare autoimmune rheumatic diseases: an observational study
Gumber, Leher; Jackson, Hannah; Gomez, Nancy; Hopkins, Georgina; Tucis, Davis; Chakravorty, Mithun; Tighe, Patrick; Grainge, Matthew J.; Rutter, Megan; Ferraro, Alastair; Power, Sheila; Pradère, Marie-Josèphe; Lanyon, Peter C.; Pearce, Fiona A.; Fairclough, Lucy
Authors
Dr HANNAH JACKSON Hannah.Jackson6@nottingham.ac.uk
RESEARCH FELLOW
Nancy Gomez
Dr GEORGINA HOPKINS Georgina.Hopkins@nottingham.ac.uk
Research Fellow
Davis Tucis
Mithun Chakravorty
Professor PATRICK TIGHE paddy.tighe@nottingham.ac.uk
PROFESSOR OF MOLECULAR IMMUNOLOGY
Dr MATTHEW GRAINGE MATTHEW.GRAINGE@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Megan Rutter
Alastair Ferraro
Sheila Power
Marie-Josèphe Pradère
Peter C. Lanyon
Dr FIONA PEARCE Fiona.Pearce@nottingham.ac.uk
CLINICAL ASSOCIATE PROFESSOR
Professor Lucy Fairclough LUCY.FAIRCLOUGH@NOTTINGHAM.AC.UK
PROFESSOR OF IMMUNOLOGY
Abstract
Objective: Antibody responses to coronavirus disease 2019 (COVID-19) vaccines are reduced among immunocompromised patients but are not well quantified among people with rare disease. We conducted an observational study to evaluate the antibody responses to the booster SARS-CoV-2 vaccine in people with rare autoimmune rheumatic diseases (RAIRD). Methods: Blood samples were collected after second, before third, after third and after fourth vaccine doses. Anti-spike and anti-nucleocapsid antibody levels were measured using an in-house ELISA. Logistic regression models were built to determine the predictors for non-response. Results were compared with age- and sex-matched healthy controls. Results: Forty-three people with RAIRD were included, with a median age of 56 years. Anti-spike seropositivity increased from 42.9% after second dose to 51.2% after third dose and 65.6% after fourth dose. Median anti-spike antibody levels increased from 33.6 (interquartile range 7.8–724.5) binding antibody units after second dose to 239.4 (interquartile range 35.8–1051.1) binding antibody units after the booster dose (third dose, or fourth dose if eligible). Of the participants who had sufficient antibody levels post-second dose, 22.2% had insufficient levels after the booster, and 34.9% of participants had lower antibodies after the booster than the lowest healthy control had after the second dose. Rituximab in the 6 months prior to booster (P = 0.02) and non-White ethnicity (P = 0.04) were associated with non-response. There was a dose–response relationship between the timing of rituximab and generation of sufficient antibodies (P = 0.03). Conclusion: Although the booster dose increased anti-spike IgG and seropositivity rates, some people with RAIRD, particularly those on rituximab, had insufficient antibody levels despite three or four doses.
Citation
Gumber, L., Jackson, H., Gomez, N., Hopkins, G., Tucis, D., Chakravorty, M., Tighe, P., Grainge, M. J., Rutter, M., Ferraro, A., Power, S., Pradère, M.-J., Lanyon, P. C., Pearce, F. A., & Fairclough, L. (2023). Antibody response to four doses of SARS-CoV-2 vaccine in rare autoimmune rheumatic diseases: an observational study. Rheumatology Advances in Practice, 7(3), Article rkad097. https://doi.org/10.1093/rap/rkad097
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 20, 2023 |
Online Publication Date | Nov 29, 2023 |
Publication Date | 2023 |
Deposit Date | Nov 14, 2023 |
Publicly Available Date | Nov 15, 2023 |
Journal | Rheumatology Advances in Practice |
Electronic ISSN | 2514-1775 |
Publisher | Oxford University Press |
Peer Reviewed | Peer Reviewed |
Volume | 7 |
Issue | 3 |
Article Number | rkad097 |
DOI | https://doi.org/10.1093/rap/rkad097 |
Keywords | rare autoimmune rheumatic diseases, SARS-CoV-2, vaccination, antibody, rituximab |
Public URL | https://nottingham-repository.worktribe.com/output/27370367 |
Publisher URL | https://academic.oup.com/rheumap/article/7/3/rkad097/7413182 |
Additional Information | © The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
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