Antibody responses to SARS-CoV-2 vaccines in 45,965 adults from the general population of the United Kingdom

Jia Wei(Open Data Institute), Nicole Stoesser(John Radcliffe Hospital), Philippa C. Matthews(John Radcliffe Hospital), Daniel Ayoubkhani(Office for National Statistics), Ruth Studley(Office for National Statistics), Iain Bell(Office for National Statistics), John I. Bell(University of Oxford), John Newton(Public Health England), Jeremy Farrar(Wellcome Trust), Ian Diamond(Office for National Statistics), Emma Rourke(Office for National Statistics), Alison Howarth(John Radcliffe Hospital), Brian D. Marsden(Nuffield Orthopaedic Centre), Sarah Hoosdally(University of Oxford), E. Yvonne Jones(University of Oxford), David I. Stuart(University of Oxford), Derrick W. Crook(John Radcliffe Hospital), Tim Peto(John Radcliffe Hospital), Koen B. Pouwels(Open Data Institute), David W. Eyre(John Radcliffe Hospital), A. Sarah Walker(Open Data Institute), the COVID-19 Infection Survey team(Office for National Statistics), Alex Lambert(Office for National Statistics), Tina Thomas(Office for National Statistics), Russell Black(Office for National Statistics), Antonio Felton(Office for National Statistics), Megan Crees(Office for National Statistics), Joel W. Jones(Office for National Statistics), Lina Lloyd(Office for National Statistics), Esther Sutherland(Office for National Statistics), Emma Pritchard(University of Oxford), Karina-Doris Vihta(University of Oxford), George Doherty(University of Oxford), James Kavanagh(University of Oxford), Kevin Chau(University of Oxford), Stephanie B. Hatch(University of Oxford), Daniel Ebner(University of Oxford), Lucas Martins Ferreira(University of Oxford), Thomas Christott(University of Oxford), Wanwisa Dejnirattisai(University of Oxford), Juthathip Mongkolsapaya(University of Oxford), Sarah Cameron(University of Oxford), Phoebe Tamblin-Hopper(University of Oxford), Magda Wolna(University of Oxford), Rachael Brown(University of Oxford), Richard J. Cornall(University of Oxford), Gavin Screaton(University of Oxford), Katrina Lythgoe(University of Oxford), David Bonsall(University of Oxford), Tanya Golubchik(University of Oxford), Helen Fryer(University of Oxford), Stuart Cox(Oxford University Hospitals NHS Trust), Kevin Paddon(Oxford University Hospitals NHS Trust), Tim James(University of Manchester), Thomas House(University of Manchester), Julie V. Robotham(Public Health England), Paul Birrell(IQVIA (United Kingdom)), Helena Jordan(IQVIA (United Kingdom)), Tim Sheppard(IQVIA (United Kingdom)), Graham Athey(IQVIA (United Kingdom)), Dan Moody(IQVIA (United Kingdom)), Leigh Curry(IQVIA (United Kingdom)), Pamela Brereton(IQVIA (United Kingdom)), Ian Jarvis, Anna Godsmark, George Morris, Bobby Mallick, Phil Eeles, Jodie Hay, Harper VanSteenhouse(Department of Health and Social Care), Jessica Lee(Department of Health and Social Care)
Nature Microbiology
July 21, 2021
Cited by 346Open Access
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Abstract

We report that in a cohort of 45,965 adults, who were receiving either the ChAdOx1 or the BNT162b2 SARS-CoV-2 vaccines, in those who had no prior infection with SARS-CoV-2, seroconversion rates and quantitative antibody levels after a single dose were lower in older individuals, especially in those aged >60 years. Two vaccine doses achieved high responses across all ages. Antibody levels increased more slowly and to lower levels with a single dose of ChAdOx1 compared with a single dose of BNT162b2, but waned following a single dose of BNT162b2 in older individuals. In descriptive latent class models, we identified four responder subgroups, including a 'low responder' group that more commonly consisted of people aged >75 years, males and individuals with long-term health conditions. Given our findings, we propose that available vaccines should be prioritized for those not previously infected and that second doses should be prioritized for individuals aged >60 years. Further data are needed to better understand the extent to which quantitative antibody responses are associated with vaccine-mediated protection.


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