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Impact of vaccination on new SARS-CoV-2 infections in the United Kingdom.
Pritchard, Emma; Matthews, Philippa C; Stoesser, Nicole; Eyre, David W; Gethings, Owen; Vihta, Karina-Doris; Jones, Joel; House, Thomas; VanSteenHouse, Harper; Bell, Iain; Bell, John I; Newton, John N; Farrar, Jeremy; Diamond, Ian; Rourke, Emma; Studley, Ruth; Crook, Derrick; Peto, Tim E A; Walker, A Sarah; Pouwels, Koen B.
  • Pritchard E; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Matthews PC; National Institute for Health Research (NIHR) Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
  • Stoesser N; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Eyre DW; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Gethings O; Department of Infectious Diseases and Microbiology, Oxford, University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
  • Vihta KD; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Jones J; National Institute for Health Research (NIHR) Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
  • House T; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
  • VanSteenHouse H; Department of Infectious Diseases and Microbiology, Oxford, University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
  • Bell I; National Institute for Health Research (NIHR) Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
  • Bell JI; NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Newton JN; Department of Infectious Diseases and Microbiology, Oxford, University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.
  • Farrar J; Big Data Institute, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Diamond I; Office for National Statistics, Newport, UK.
  • Rourke E; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Studley R; National Institute for Health Research (NIHR) Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford, UK.
  • Crook D; Office for National Statistics, Newport, UK.
  • Peto TEA; Department of Mathematics, University of Manchester, Manchester, UK.
  • Walker AS; IBM Research, Hartree Centre, Daresbury, UK.
  • Pouwels KB; Glasgow Lighthouse Laboratory, Glasgow, UK.
Nat Med ; 27(8): 1370-1378, 2021 08.
Article in English | MEDLINE | ID: covidwho-1263502
ABSTRACT
The effectiveness of COVID-19 vaccination in preventing new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections in the general community is still unclear. Here, we used the Office for National Statistics COVID-19 Infection Survey-a large community-based survey of individuals living in randomly selected private households across the United Kingdom-to assess the effectiveness of the BNT162b2 (Pfizer-BioNTech) and ChAdOx1 nCoV-19 (Oxford-AstraZeneca; ChAdOx1) vaccines against any new SARS-CoV-2 PCR-positive tests, split according to self-reported symptoms, cycle threshold value (<30 versus ≥30; as a surrogate for viral load) and gene positivity pattern (compatible with B.1.1.7 or not). Using 1,945,071 real-time PCR results from nose and throat swabs taken from 383,812 participants between 1 December 2020 and 8 May 2021, we found that vaccination with the ChAdOx1 or BNT162b2 vaccines already reduced SARS-CoV-2 infections ≥21 d after the first dose (61% (95% confidence interval (CI) = 54-68%) versus 66% (95% CI = 60-71%), respectively), with greater reductions observed after a second dose (79% (95% CI = 65-88%) versus 80% (95% CI = 73-85%), respectively). The largest reductions were observed for symptomatic infections and/or infections with a higher viral burden. Overall, COVID-19 vaccination reduced the number of new SARS-CoV-2 infections, with the largest benefit received after two vaccinations and against symptomatic and high viral burden infections, and with no evidence of a difference between the BNT162b2 and ChAdOx1 vaccines.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Observational study / Randomized controlled trials Topics: Vaccines Limits: Humans Country/Region as subject: Europa Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2021 Document Type: Article Affiliation country: S41591-021-01410-w

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Observational study / Randomized controlled trials Topics: Vaccines Limits: Humans Country/Region as subject: Europa Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2021 Document Type: Article Affiliation country: S41591-021-01410-w