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SARS-CoV-2 antibody trajectories after a single COVID-19 vaccination with and without prior infection.
Wei, Jia; Matthews, Philippa C; Stoesser, Nicole; Diamond, Ian; Studley, Ruth; Rourke, Emma; Cook, Duncan; Bell, John I; Newton, John N; Farrar, Jeremy; Howarth, Alison; Marsden, Brian D; Hoosdally, Sarah; Jones, E Yvonne; Stuart, David I; Crook, Derrick W; Peto, Tim E A; Walker, A Sarah; Eyre, David W; Pouwels, Koen B.
  • Wei J; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Matthews PC; Big Data Institute, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Stoesser N; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Diamond I; The Francis Crick Institute, 1 Midland Road, London, UK.
  • Studley R; Division of infection and immunity, University College London, London, UK.
  • Rourke E; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Cook D; Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
  • Bell JI; The National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford, Oxford, UK.
  • Newton JN; The National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Farrar J; Office for National Statistics, Newport, UK.
  • Howarth A; Office for National Statistics, Newport, UK.
  • Marsden BD; Office for National Statistics, Newport, UK.
  • Hoosdally S; Office for National Statistics, Newport, UK.
  • Jones EY; Office of the Regius Professor of Medicine, University of Oxford, Oxford, UK.
  • Stuart DI; European Centre for Environment and Human Health, University of Exeter, Truro, UK.
  • Crook DW; Wellcome Trust, London, UK.
  • Peto TEA; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Walker AS; Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
  • Eyre DW; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Pouwels KB; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Nat Commun ; 13(1): 3748, 2022 06 29.
Article in English | MEDLINE | ID: covidwho-1908182
ABSTRACT
Given high SARS-CoV-2 incidence, coupled with slow and inequitable vaccine roll-out in many settings, there is a need for evidence to underpin optimum vaccine deployment, aiming to maximise global population immunity. We evaluate whether a single vaccination in individuals who have already been infected with SARS-CoV-2 generates similar initial and subsequent antibody responses to two vaccinations in those without prior infection. We compared anti-spike IgG antibody responses after a single vaccination with ChAdOx1, BNT162b2, or mRNA-1273 SARS-CoV-2 vaccines in the COVID-19 Infection Survey in the UK general population. In 100,849 adults median (50 (IQR 37-63) years) receiving at least one vaccination, 13,404 (13.3%) had serological/PCR evidence of prior infection. Prior infection significantly boosted antibody responses, producing higher peak levels and/or longer half-lives after one dose of all three vaccines than those without prior infection receiving one or two vaccinations. In those with prior infection, the median time above the positivity threshold was >1 year after the first vaccination. Single-dose vaccination targeted to those previously infected may provide at least as good protection to two-dose vaccination among those without previous infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Type of study: Experimental Studies / Observational study Topics: Vaccines Limits: Adult / Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-31495-x

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Type of study: Experimental Studies / Observational study Topics: Vaccines Limits: Adult / Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-31495-x