Evidence map›Paper›PMID 37590132›Full record

ArticleCell reports2023

Atypical B cells and impaired SARS-CoV-2 neutralization following heterologous vaccination in the elderly.

Isabella A T M Ferreira, Colin Y C Lee, William S Foster, Adam Abdullahi, Lisa M Dratva, Zewen Kelvin Tuong, Benjamin J Stewart, John R Ferdinand, Stephane M Guillaume, Martin O P Potts and 23 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

16 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Atypical and non-classical CD45RBNature communications · 2024
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

33 authors at 10 institutions in 2 countries.

Isabella A T M FerreiraCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Colin Y C LeeMolecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK; Cellular Genetics, Wellcome Sanger Institute, Cambridge, UK.
William S FosterImmunology Programme, Babraham Institute, Babraham Research Campus, Cambridge, UK.
Adam AbdullahiCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Lisa M DratvaCellular Genetics, Wellcome Sanger Institute, Cambridge, UK.
Zewen Kelvin TuongMolecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK; Cellular Genetics, Wellcome Sanger Institute, Cambridge, UK.
Benjamin J StewartMolecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK; Cellular Genetics, Wellcome Sanger Institute, Cambridge, UK.
John R FerdinandMolecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK.
Stephane M GuillaumeImmunology Programme, Babraham Institute, Babraham Research Campus, Cambridge, UK.
Martin O P PottsCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Marianne PereraCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Benjamin A KrishnaCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Ana PeñalverMolecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK.
Mia CabantousMolecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK.
Steven A KempCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Lourdes Ceron-GutierrezDepartment of Clinical Biochemistry and Immunology, Cambridge University Hospital NHS Trust, Cambridge, UK.
Soraya EbrahimiDepartment of Clinical Biochemistry and Immunology, Cambridge University Hospital NHS Trust, Cambridge, UK.
CITIID-NIHR BioResource COVID-19 Collaboration
Paul LyonsCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Kenneth G C SmithCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
John BradleyCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Dami A CollierCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Laura E McCoyDivision of Infection and Immunity, UCL, London, UK.
Agatha van der KlaauwUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-Medical Research Council (MRC) Institute of Metabolic Science, Cambridge, UK.
James E D ThaventhiranMRC Toxicology Unit, University of Cambridge, Cambridge, UK.
I Sadaf FarooqiUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-Medical Research Council (MRC) Institute of Metabolic Science, Cambridge, UK.
Sarah A TeichmannCellular Genetics, Wellcome Sanger Institute, Cambridge, UK.
Paul A MacAryNational University of Singapore, Singapore, Singapore.
Rainer DoffingerDepartment of Clinical Biochemistry and Immunology, Cambridge University Hospital NHS Trust, Cambridge, UK.
Mark R WillsCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK.
Michelle A LintermanImmunology Programme, Babraham Institute, Babraham Research Campus, Cambridge, UK. Electronic address: michelle.linterman@babraham.ac.uk.
Menna R ClatworthyCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK; Molecular Immunity Unit, Department of Medicine, Medical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge, UK; Cellular Genetics, Wellcome Sanger Institute, Cambridge, UK. Electronic address: mrc38@medschl.cam.ac.uk.
Ravindra K GuptaCambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge, UK; Department of Medicine, University of Cambridge, Cambridge, UK. Electronic address: rkg20@cam.ac.uk.
University of Cambridge · GBBabraham Institute · GBCambridge University Hospitals NHS Foundation Trust · GBMRC Laboratory of Molecular Biology · GBWellcome Sanger Institute · GBMRC Toxicology Unit · GBNational University of Singapore · SGNIHR Cambridge Biomedical Research CentreUniversity College London · GBWellcome/MRC Institute of Metabolic Science · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/000C0427Biotechnology and Biological Sciences Research Council BBS/E/B/000C0428Department of Health NIHR203312Department of Health RP-2017-08-ST2-002Medical Research Council MC_UU_0025/12Medical Research Council MR/S00081X/1Medical Research Council MR/W020564/1MRF_ MRF-057-0002-RG-THAV-C0798Wellcome Trust 207462/Z/17/ZWellcome Trust 220268/Z/20/ZWellcome Trust WT108082AIA
6 · The paper itself

Abstract

Suboptimal responses to a primary vaccination course have been reported in the elderly, but there is little information regarding the impact of age on responses to booster third doses. Here, we show that individuals 70 years or older (median age 73, range 70-75) who received a primary two-dose schedule with AZD1222 and booster third dose with mRNA vaccine achieve significantly lower neutralizing antibody responses against SARS-CoV-2 spike pseudotyped virus compared with those younger than 70 (median age 66, range 54-69) at 1 month post booster. Impaired neutralization potency and breadth post third dose in the elderly is associated with circulating "atypical" spike-specific B cells expressing CD11c and FCRL5. However, when considering individuals who received three doses of mRNA vaccine, we did not observe differences in neutralization or enrichment in atypical B cells. This work highlights the finding that AdV and mRNA COVID-19 vaccine formats differentially instruct the memory B cell response.

Indexed as

COVID-19AgedChAdOx1 nCoV-19COVID-19 VaccinesHumansSARS-CoV-2VaccinationChAdOx1 nCoV-19COVID-19 VaccinesAZD1222BNT162b2CP: ImmunologyelderlySARS-CoV-2

Identifiers

PMID37590132
PMCPMC7619014
OpenAlexW4385969518

What OpenQuestion holds

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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.