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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.

Two doses of the SARS-CoV-2 BNT162b2 vaccine enhance antibody responses to variants in individuals with prior SARS-CoV-2 infection Thumbnail


Authors

Richard A. Urbanowicz

Theocharis Tsoleridis

Hannah J. Jackson

Lola Cusin

Joshua D. Duncan

Joseph G. Chappell

Jessica Nightingale

Alan R. Norrish

Adeel Ikram

Dr BEN MARSON Ben.Marson@nottingham.ac.uk
Clinical Associate Professor

Simon J. Craxford

Anthony Kelly

Jonathan K. Ball

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

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