Evidence map›Paper›PMID 34260717›Full record

ArticleThe Journal of infectious diseases2021

SARS-CoV-2 B.1.617 Mutations L452R and E484Q Are Not Synergistic for Antibody Evasion.

Isabella A T M Ferreira, Steven A Kemp, Rawlings Datir, Akatsuki Saito, Bo Meng, Partha Rakshit, Akifumi Takaori-Kondo, Yusuke Kosugi, Keiya Uriu, Izumi Kimura and 9 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

98 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. COVID-19 pandemic: the delta variant, T-cell responses, and the efficacy of developing vaccines.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Pooled it
  2. Novel AfricanJournal of virology · 2026
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38 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Isabella A T M FerreiraCambridge Institute of Therapeutic Immunology and Infectious Disease, Cambridge,United Kingdom.
Steven A KempCambridge Institute of Therapeutic Immunology and Infectious Disease, Cambridge,United Kingdom.
Rawlings DatirCambridge Institute of Therapeutic Immunology and Infectious Disease, Cambridge,United Kingdom.
Akatsuki SaitoDepartment of Veterinary Medicine, Faculty of Agriculture, University of Miyazaki, Miyazaki,Japan.
Bo MengCambridge Institute of Therapeutic Immunology and Infectious Disease, Cambridge,United Kingdom.
Partha RakshitNational Centre for Disease Control, Delhi,India.
Akifumi Takaori-KondoDepartment of Hematology and Oncology, Kyoto University, Kyoto,Japan.
Yusuke KosugiDivision of Systems Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Keiya UriuDivision of Systems Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Izumi KimuraDivision of Systems Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Kotaro ShirakawaDepartment of Hematology and Oncology, Kyoto University, Kyoto,Japan.
Adam AbdullahiCambridge Institute of Therapeutic Immunology and Infectious Disease, Cambridge,United Kingdom.
Anurag AgarwalCSIR Institute of Genomics and Integrative Biology, Delhi,India.
Seiya OzonoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo,Japan.
Kenzo TokunagaDepartment of Pathology, National Institute of Infectious Diseases, Tokyo,Japan.
Kei SatoDivision of Systems Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.ORCID 0000-0003-4431-1380
Ravindra K GuptaCambridge Institute of Therapeutic Immunology and Infectious Disease, Cambridge,United Kingdom.ORCID 0000-0001-9751-1808
CITIID-NIHR BioResource COVID-19 Collaboration, Indian SARS-CoV-2 Genomics Consortium
Genotype to Phenotype Japan (G2P-Japan) Consortium

Funding

Wellcome Trust WT108082AIA
6 · The paper itself

Abstract

The SARS-CoV-2 B.1.617 variant emerged in the Indian state of Maharashtra in late 2020. There have been fears that 2 key mutations seen in the receptor-binding domain, L452R and E484Q, would have additive effects on evasion of neutralizing antibodies. We report that spike bearing L452R and E484Q confers modestly reduced sensitivity to BNT162b2 mRNA vaccine-elicited antibodies following either first or second dose. The effect is similar in magnitude to the loss of sensitivity conferred by L452R or E484Q alone. These data demonstrate reduced sensitivity to vaccine-elicited neutralizing antibodies by L452R and E484Q but lack of synergistic loss of sensitivity.

Indexed as

Immune EvasionMutationAngiotensin-Converting Enzyme 2AnimalsAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineChlorocebus aethiopsCOVID-19COVID-19 VaccinesHEK293 CellsHumansIndiaProtein BindingSARS-CoV-2Serine EndopeptidasesACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesSerine EndopeptidasesSpike Glycoprotein, CoronavirusTMPRSS2 protein, humanantibody escapeB.1.617COVID-19evasionfitnessIndian variantinfectivityneutralizing antibodiesresistanceSARS-CoV-2spike mutation

Identifiers

PMID34260717
PMCPMC8420622

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.