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Antibody levels following vaccination against SARS-CoV-2: associations with post-vaccination infection and risk factors in two UK longitudinal studies

Antibody levels following vaccination against SARS-CoV-2: associations with post-vaccination infection and risk factors in two UK longitudinal studies
Antibody levels following vaccination against SARS-CoV-2: associations with post-vaccination infection and risk factors in two UK longitudinal studies
Background: severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody levels can be used to assess humoral immune responses following SARS-CoV-2 infection or vaccination, and may predict risk of future infection. Higher levels of SARS-CoV-2 anti-Spike antibodies are known to be associated with increased protection against future SARS-CoV-2 infection. However, variation in antibody levels and risk factors for lower antibody levels following each round of SARS-CoV-2 vaccination have not been explored across a wide range of socio-demographic, SARS-CoV-2 infection and vaccination, and health factors within population-based cohorts.

Methods: samples were collected from 9361 individuals from TwinsUK and ALSPAC UK population-based longitudinal studies and tested for SARS-CoV-2 antibodies. Cross-sectional sampling was undertaken jointly in April-May 2021 (TwinsUK, N=4256; ALSPAC, N=4622), and in TwinsUK only in November 2021-January 2022 (N=3575). Variation in antibody levels after first, second, and third SARS-CoV-2 vaccination with health, socio-demographic, SARS-CoV-2 infection, and SARS-CoV-2 vaccination variables were analysed. Using multivariable logistic regression models, we tested associations between antibody levels following vaccination and: (1) SARS-CoV-2 infection following vaccination(s); (2) health, socio-demographic, SARS-CoV-2 infection, and SARS-CoV-2 vaccination variables.

Results: within TwinsUK, single-vaccinated individuals with the lowest 20% of anti-Spike antibody levels at initial testing had threefold greater odds of SARS-CoV-2 infection over the next 6–9 months (OR = 2.9, 95% CI: 1.4, 6.0), compared to the top 20%. In TwinsUK and ALSPAC, individuals identified as at increased risk of COVID-19 complication through the UK ‘Shielded Patient List’ had consistently greater odds (two- to fourfold) of having antibody levels in the lowest 10%. Third vaccination increased absolute antibody levels for almost all individuals, and reduced relative disparities compared with earlier vaccinations.

Conclusions: these findings quantify the association between antibody level and risk of subsequent infection, and support a policy of triple vaccination for the generation of protective antibodies.
2050-084X
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Cheetham, Nathan J., Kibble, Milla, Wong, Andrew, Silverwood, Richard J., Knuppel, Anika, Williams, Dylan M., Hamilton, Olivia K.L., Lee, Paul H., Staatz, Charis Bridger, Gessa, Giorgio Di, Zhu, Jingmin, Katikireddi, Srinivasa Vittal, Ploubidis, George B., Thompson, Ellen J., Bowyer, Ruth C.E., Zhang, Xinyuan, Abbasian, Golboo, Garcia, Maria Paz, Hart, Deborah, Seow, Jeffrey, Graham, Carl, Kouphou, Neophytos, Acors, Sam, Malim, Michael H., Mitchell, Ruth E., Northstone, Kate, Major-Smith, Daniel, Matthews, Sarah, Breeze, Thomas, Crawford, Michael, Molloy, Lynn, Kwong, Alex S.F., Doores, Katie, Chaturvedi, Nishi, Duncan, Emma L., Timpson, Nicholas J and Steves, Claire J. (2023) Antibody levels following vaccination against SARS-CoV-2: associations with post-vaccination infection and risk factors in two UK longitudinal studies. eLife, 12, [e80428]. (doi:10.7554/eLife.80428).

Record type: Article

Abstract

Background: severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody levels can be used to assess humoral immune responses following SARS-CoV-2 infection or vaccination, and may predict risk of future infection. Higher levels of SARS-CoV-2 anti-Spike antibodies are known to be associated with increased protection against future SARS-CoV-2 infection. However, variation in antibody levels and risk factors for lower antibody levels following each round of SARS-CoV-2 vaccination have not been explored across a wide range of socio-demographic, SARS-CoV-2 infection and vaccination, and health factors within population-based cohorts.

Methods: samples were collected from 9361 individuals from TwinsUK and ALSPAC UK population-based longitudinal studies and tested for SARS-CoV-2 antibodies. Cross-sectional sampling was undertaken jointly in April-May 2021 (TwinsUK, N=4256; ALSPAC, N=4622), and in TwinsUK only in November 2021-January 2022 (N=3575). Variation in antibody levels after first, second, and third SARS-CoV-2 vaccination with health, socio-demographic, SARS-CoV-2 infection, and SARS-CoV-2 vaccination variables were analysed. Using multivariable logistic regression models, we tested associations between antibody levels following vaccination and: (1) SARS-CoV-2 infection following vaccination(s); (2) health, socio-demographic, SARS-CoV-2 infection, and SARS-CoV-2 vaccination variables.

Results: within TwinsUK, single-vaccinated individuals with the lowest 20% of anti-Spike antibody levels at initial testing had threefold greater odds of SARS-CoV-2 infection over the next 6–9 months (OR = 2.9, 95% CI: 1.4, 6.0), compared to the top 20%. In TwinsUK and ALSPAC, individuals identified as at increased risk of COVID-19 complication through the UK ‘Shielded Patient List’ had consistently greater odds (two- to fourfold) of having antibody levels in the lowest 10%. Third vaccination increased absolute antibody levels for almost all individuals, and reduced relative disparities compared with earlier vaccinations.

Conclusions: these findings quantify the association between antibody level and risk of subsequent infection, and support a policy of triple vaccination for the generation of protective antibodies.

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Accepted/In Press date: 22 December 2022
e-pub ahead of print date: 24 January 2023
Published date: 20 February 2023
Additional Information: Funding Information: is funded by COVID-19 Longitudinal Health and Wellbeing – National Core Study (LHW-NCS). Antibody testing was funded by UK Health Security Agency. The National Core Studies program. NJT is a Wellcome Trust Investigator (202802/Z/16/Z), is the PI of the Avon Longitudinal Study of Parents and Children (MRC & WT 217065/Z/19/Z), is supported by the University of Bristol NIHR Biomedical Research Centre (BRC-1215-2001), the MRC Integrative Epidemiology Unit (MC_UU_00011/1) and works within the CRUK Integrative Cancer Epidemiology Programme (C18281/A29019). MK is supported by the Medical Research Council (MR/W021315/1). AK is supported by Characterisation, determinants, mechanisms and consequences of the long-term effects of COVID-19: providing the evidence base for health care services (CONVALESCENCE) funded by NIHR (COV-LT-0009). SVK acknowledges funding from an NRS Senior Clinical Fellowship (SCAF/15/02), the Medical Research Council (MC_UU_00022/2) and the Scottish Government Chief Scientist Office (SPHSU17). OKLH is supported by the Medical Research Council (MC_UU_12017/11 and MC_UU_00022/3) and the Scottish Government Chief Scientist Office (SPHSU17).This publication is the work of the authors and NJC, NJT and CJS serve as guarantors for the contents of this paper. HMT/UKRI/MRC (MC_PC_20030 & MC_PC_20059). Related funding was also provided by the NIHR 606 (CONVALESCENCE grant COV-LT-0009). TwinsUK is funded by the Wellcome Trust, Medical Research Council, Versus Arthritis, European Union Horizon 2020, Chronic Disease Research Foundation (CDRF), Zoe Ltd and the National Institute for Health Research (NIHR) Clinical Research Network (CRN) and Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London. The UK Medical Research Council and Wellcome (Grant ref: 217065/Z/19/Z) and the University of Bristol provide core support for ALSPAC.

Identifiers

Local EPrints ID: 479827
URI: http://eprints.soton.ac.uk/id/eprint/479827
ISSN: 2050-084X
PURE UUID: 73d55581-68d5-4593-a637-ac737a2ef340

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Date deposited: 27 Jul 2023 13:50
Last modified: 17 Mar 2024 03:32

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Contributors

Author: Nathan J. Cheetham
Author: Milla Kibble
Author: Andrew Wong
Author: Richard J. Silverwood
Author: Anika Knuppel
Author: Dylan M. Williams
Author: Olivia K.L. Hamilton
Author: Paul H. Lee
Author: Charis Bridger Staatz
Author: Giorgio Di Gessa
Author: Jingmin Zhu
Author: Srinivasa Vittal Katikireddi
Author: George B. Ploubidis
Author: Ellen J. Thompson
Author: Ruth C.E. Bowyer
Author: Xinyuan Zhang
Author: Golboo Abbasian
Author: Maria Paz Garcia
Author: Deborah Hart
Author: Jeffrey Seow
Author: Carl Graham
Author: Neophytos Kouphou
Author: Sam Acors
Author: Michael H. Malim
Author: Ruth E. Mitchell
Author: Kate Northstone
Author: Daniel Major-Smith
Author: Sarah Matthews
Author: Thomas Breeze
Author: Michael Crawford
Author: Lynn Molloy
Author: Alex S.F. Kwong
Author: Katie Doores
Author: Nishi Chaturvedi
Author: Emma L. Duncan
Author: Nicholas J Timpson
Author: Claire J. Steves

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