Cited by 2,889SARS-CoV-2 and COVID-19 ResearchVaccine Coverage and HesitancyCOVID-19 epidemiological studies

The DOI matches its Crossref record; 27 of the 28 references it cites were found in a registry or an index, and 1 are not checked yet; none of the 18 sources its claims cite is checked for support yet.

Effectiveness of Covid-19 Vaccines against the B.1.617.2 (Delta) Variant

Open access

Published version of a preprint

Abstract

Abstract Background The B.1.617.2 COVID-19 variant has contributed to the surge in cases in India and has now been detected across the globe, including a notable increase in cases in the UK. We estimate the effectiveness of the BNT162b2 and ChAdOx1 COVID-19 vaccines against this variant. Methods A test negative case control design was used to estimate the effectiveness of vaccination against symptomatic disease with both variants over the period that B.1.617.2 began circulating with cases identified based on sequencing and S-gene target status. Data on all symptomatic sequenced cases of COVID-19 in England was used to estimate the proportion of cases with B.1.617.2 compared to the predominant strain (B.1.1.7) by vaccination status. Results Effectiveness was notably lower after 1 dose of vaccine with B.1.617.2 cases 33.5% (95%CI: 20.6 to 44.3) compared to B.1.1.7 cases 51.1% (95%CI: 47.3 to 54.7) with similar results for both vaccines. With BNT162b2 2 dose effectiveness reduced from 93.4% (95%CI: 90.4 to 95.5) with B.1.1.7 to 87.9% (95%CI: 78.2 to 93.2) with B.1.617.2. With ChAdOx1 2 dose effectiveness reduced from 66.1% (95% CI: 54.0 to 75.0) with B.1.1.7 to 59.8% (95%CI: 28.9 to 77.3) with B.1.617.2. Sequenced cases detected after 1 or 2 doses of vaccination had a higher odds of infection with B.1.617.2 compared to unvaccinated cases (OR 1.40; 95%CI: 1.13-1.75). Conclusions After 2 doses of either vaccine there were only modest differences in vaccine effectiveness with the B.1.617.2 variant. Absolute differences in vaccine effectiveness were more marked with dose 1. This would support maximising vaccine uptake with two doses among vulnerable groups.

Checked 2026-10-06 · 1 reference not checked yet

Overview

Integrity signals

Registry

Crossref · 10.1056/nejmoa2108891

Cites

27 of 28 references verified0 citation errors · 0 not checkable

Statistics

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Verification

Claims the paper makes

0 of 18 cited sources checked · 0 supported · 0 flagged

  • It may state two separate claims as one. 17
  • The quote only partly states this claim. 2
  • Probably not a substantial claim. 8
22 of 22
  • The authors state this as an assumption.

    For the secondary analysis, if a vaccine had some efficacy and was equally effective against both variants, a similar proportion of cases with either variant would be expected in unvaccinated and vaccinated persons; if the vaccine was less effective against delta than alpha, delta would make up a higher proportion of cases occurring more than 3 weeks after vaccination than among unvaccinated.

    “The underlying assumption was that if the vaccine had some efficacy and was equally effective against each variant, a similar proportion of cases with either variant would be expected in unvaccinated persons and in vaccinated persons. Conversely, if the vaccine was less effective against the delta variant than against the alpha variant, then the delta variant would be expected to make up a higher”
  • The authors state this as an assumption.

    The accuracy of sequencing would not depend on the variant.

    “that is, the accuracy of the sequencing would not depend on the variant”
  • The authors state this as an assumption.

    The propensity among symptomatic persons to get tested would not differ according to variant.

    “and the propensity among symptomatic persons to get tested would not differ according to variant.”
  • The paper relies on this without support.

    The effectiveness of BNT162b2 and ChAdOx1 nCoV-19 against the delta variant was unclear or limited before this study.

    “The effectiveness of the BNT162b2 and ChAdOx1 nCoV-19 vaccines against this variant has been unclear.”
    “Data on the effectiveness of Covid-19 vaccines against clinical outcomes with this variant have been limited.”
4 of 4

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Metadata

Authors
Lopez Bernal, J., Andrews, N., Gower, C., Gallagher, E., Simmons, R., Thelwall, S., Stowe, J., Tessier, E., Groves, N., Dabrera, G., Myers, R., Campbell, C. N. J., Amirthalingam, G., Edmunds, M., Zambon, M., Brown, K. E., Hopkins, S., Chand, M., & Ramsay, M.
Affiliations
  • From Public Health England (J.L.B., N.A., C.G., E.G., R.S., S.T., J.S., E.T., N.G., G.D., R.M., C.N.J.C., G.A., M.E., M.Z., K.E.B., S.H., M.C., M.R.), the National Institute of Health Research (NIHR) Health Protection Research Unit in Vaccines and Immunisation, London School of Hygiene and Tropical Medicine (J.L.B., N.A., C.N.J.C., G.A., K.E.B., M.R.), the NIHR Health Protection Research Unit in Respiratory Infections, Imperial College London (J.L.B., M.Z.), and Guy’s and St. Thomas’ Hospital NHS Trust (M.C.), London, and Healthcare Associated Infections and Antimicrobial Resistance, University of Oxford, Oxford (S.H.) — all in the United Kingdom.
  • Public Health England (GB)
Venue
New England Journal of Medicine
Published
2021-08-12
Volume
385
Issue
7
Pages
585-594
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W3184226105
Cited by
2,889
References
26
Citations by year
2026: 37 · 2025: 82 · 2024: 184 · 2023: 431 · 2022: 1320 · 2021: 832
FWCI
219.33
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • New England Journal of Medicine (publishedVersion)
  • medRxiv (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Wellcome Trust
  • Public Health England
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Social Sciences › Health › Vaccine Coverage and Hesitancy
  • Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
Keywords
COVID-19 vaccines, B.1.1.7 Alpha variant, vaccine effectiveness, BNT162b2, ChAdOx1 nCoV-19 vaccine, two-dose vaccination, symptomatic COVID-19, test-negative case-control design
MeSH terms
Immunogenicity, Vaccine, COVID-19, SARS-CoV-2, COVID-19 Vaccines, Adolescent, Adult, Aged, Aged, 80 and over, Female, United Kingdom, Humans, Male, Middle Aged, Case-Control Studies, Treatment Outcome, Young Adult, Vaccine Potency

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