Antibody responses and correlates of protection in the general population after two doses of the ChAdOx1 or BNT162b2 vaccines

Jia Wei(Open Data Institute), Koen B. Pouwels(National Institute for Health and Care Research), Nicole Stoesser(John Radcliffe Hospital), Philippa C. Matthews(John Radcliffe Hospital), Ian Diamond(Office for National Statistics), Ruth Studley(Office for National Statistics), Emma Rourke(Office for National Statistics), Duncan Cook(Office for National Statistics), John I. Bell(University of Oxford), John Newton(Public Health England), Jeremy Farrar(Wellcome Trust), 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), A. Sarah Walker(Open Data Institute), David W. Eyre(John Radcliffe Hospital), the COVID-19 Infection Survey team(Office for National Statistics), Tina Thomas(Office for National Statistics), Daniel Ayoubkhani(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(University of Oxford), 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(Open Data Institute), Katrina Lythgoe(Open Data Institute), David Bonsall(Open Data Institute), Tanya Golubchik(Open Data Institute), Helen Fryer(Oxford University Hospitals NHS Trust), Stuart Cox(Oxford University Hospitals NHS Trust), Kevin Paddon(Oxford University Hospitals NHS Trust), Tim James(University of Manchester), Thomas House(Public Health England), 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, Ian Jarvis, Anna Godsmark, George Morris, Bobby Mallick, Phil Eeles, Jodie Hay, Harper VanSteenhouse(Department of Health and Social Care), Jessica Lee(Welsh Government), Sean White(Welsh Government), Tim Evans(Welsh Government), Lisa Bloemberg(Scottish Government), Katie Allison(Scottish Government), Anouska Pandya(Scottish Government), Sophie Davis(Public Health Scotland), David I. Conway(Public Health Scotland), Margaret MacLeod(Public Health Scotland), Chris Cunningham
Nature Medicine
February 14, 2022
Cited by 268Open Access
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Abstract

Antibody responses are an important part of immunity after Coronavirus Disease 2019 (COVID-19) vaccination. However, antibody trajectories and the associated duration of protection after a second vaccine dose remain unclear. In this study, we investigated anti-spike IgG antibody responses and correlates of protection after second doses of ChAdOx1 or BNT162b2 vaccines for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the United Kingdom general population. In 222,493 individuals, we found significant boosting of anti-spike IgG by the second doses of both vaccines in all ages and using different dosing intervals, including the 3-week interval for BNT162b2. After second vaccination, BNT162b2 generated higher peak levels than ChAdOX1. Older individuals and males had lower peak levels with BNT162b2 but not ChAdOx1, whereas declines were similar across ages and sexes with ChAdOX1 or BNT162b2. Prior infection significantly increased antibody peak level and half-life with both vaccines. Anti-spike IgG levels were associated with protection from infection after vaccination and, to an even greater degree, after prior infection. At least 67% protection against infection was estimated to last for 2-3 months after two ChAdOx1 doses, for 5-8 months after two BNT162b2 doses in those without prior infection and for 1-2 years for those unvaccinated after natural infection. A third booster dose might be needed, prioritized to ChAdOx1 recipients and those more clinically vulnerable.


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