Richard A. Urbanowicz
Two doses of the SARS-CoV-2 BNT162b2 vaccine enhance antibody responses to variants in individuals with prior SARS-CoV-2 infection
Urbanowicz, Richard A.; Tsoleridis, Theocharis; Jackson, Hannah J.; Cusin, Lola; Duncan, Joshua D.; Chappell, Joseph G.; Tarr, Alexander W.; Nightingale, Jessica; Norrish, Alan R.; Ikram, Adeel; Marson, Ben; Craxford, Simon J.; Kelly, Anthony; Aithal, Guruprasad P.; Vijay, Amrita; Tighe, Patrick J.; Ball, Jonathan K.; Valdes, Ana M.; Ollivere, Benjamin J.
Authors
Theocharis Tsoleridis
Hannah J. Jackson
Lola Cusin
Joshua D. Duncan
Joseph G. Chappell
Dr ALEXANDER TARR alex.tarr@nottingham.ac.uk
ASSOCIATE PROFESSOR
Jessica Nightingale
Alan R. Norrish
Adeel Ikram
Dr BEN MARSON Ben.Marson@nottingham.ac.uk
Clinical Associate Professor
Simon J. Craxford
Anthony Kelly
Professor GURUPRASAD AITHAL Guru.Aithal@nottingham.ac.uk
PROFESSOR OF HEPATOLOGY
Dr AMRITA VIJAY Amrita.Vijay@nottingham.ac.uk
RESEARCH FELLOW
Professor PATRICK TIGHE paddy.tighe@nottingham.ac.uk
PROFESSOR OF MOLECULAR IMMUNOLOGY
Jonathan K. Ball
Professor ANA VALDES Ana.Valdes@nottingham.ac.uk
PROFESSOR OF MOLECULAR & GENETIC EPIDEMIOLOGY
Benjamin J. Ollivere
Abstract
Understanding the impact of prior infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on the response to vaccination is a priority for responding to the coronavirus disease 2019 (COVID-19) pandemic. In particular, it is necessary to understand how prior infection plus vaccination can modulate immune responses against variants of concern. To address this, we sampled 20 individuals with and 25 individuals without confirmed previous SARS-CoV-2 infection from a large cohort of health care workers followed serologically since April 2020. All 45 individuals had received two doses of the Pfizer-BioNTech BNT162b2 vaccine with a delayed booster at 10 weeks. Absolute and neutralizing antibody titers against wild-type SARS-CoV-2 and variants were measured using enzyme immunoassays and pseudotype neutralization assays. We observed antibody reactivity against lineage A, B.1.351, and P.1 variants with increasing antigenic exposure, through either vaccination or natural infection. This improvement was further confirmed in neutralization assays using fixed dilutions of serum samples. The impact of antigenic exposure was more evident in enzyme immunoassays measuring SARS-CoV-2 spike protein–specific IgG antibody concentrations. Our data show that multiple exposures to SARS-CoV-2 spike protein in the context of a delayed booster expand the neutralizing breadth of the antibody response to neutralization-resistant SARS-CoV-2 variants. This suggests that additional vaccine boosts may be beneficial in improving immune responses against future SARS-CoV-2 variants of concern.
Citation
Urbanowicz, R. A., Tsoleridis, T., Jackson, H. J., Cusin, L., Duncan, J. D., Chappell, J. G., Tarr, A. W., Nightingale, J., Norrish, A. R., Ikram, A., Marson, B., Craxford, S. J., Kelly, A., Aithal, G. P., Vijay, A., Tighe, P. J., Ball, J. K., Valdes, A. M., & Ollivere, B. J. (2021). Two doses of the SARS-CoV-2 BNT162b2 vaccine enhance antibody responses to variants in individuals with prior SARS-CoV-2 infection. Science Translational Medicine, 13(609), Article eabj0847. https://doi.org/10.1126/scitranslmed.abj0847
Journal Article Type | Article |
---|---|
Acceptance Date | Jul 30, 2021 |
Online Publication Date | Aug 5, 2021 |
Publication Date | 2021-09 |
Deposit Date | Aug 2, 2022 |
Publicly Available Date | Aug 5, 2022 |
Journal | Science Translational Medicine |
Print ISSN | 1946-6234 |
Electronic ISSN | 1946-6242 |
Publisher | American Association for the Advancement of Science |
Peer Reviewed | Peer Reviewed |
Volume | 13 |
Issue | 609 |
Article Number | eabj0847 |
DOI | https://doi.org/10.1126/scitranslmed.abj0847 |
Keywords | General Medicine |
Public URL | https://nottingham-repository.worktribe.com/output/6350240 |
Publisher URL | https://www.science.org/doi/10.1126/scitranslmed.abj0847 |
Files
Scitranslmed.abj0847
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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