Evidence map›Paper›PMID 36159846›Full record

ArticleFrontiers in immunology2022

mRNA vaccination drives differential mucosal neutralizing antibody profiles in naïve and SARS-CoV-2 previously-infected individuals.

Stephanie Longet, Alexander Hargreaves, Saoirse Healy, Rebecca Brown, Hailey R Hornsby, Naomi Meardon, Tom Tipton, Eleanor Barnes, Susanna Dunachie, Christopher J A Duncan and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

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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

15 authors at 9 institutions in 2 countries.

Stephanie LongetWellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Alexander HargreavesWellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Saoirse HealyWellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Rebecca BrownDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Hailey R HornsbyDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Naomi MeardonSheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Tom TiptonWellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Eleanor BarnesNuffield Department of Clinical Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Susanna DunachieNuffield Department of Clinical Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Christopher J A DuncanTranslational and Clinical Research Institute Immunity and Inflammation Theme, Newcastle University, Newcastle, United Kingdom.
Paul KlenermanNuffield Department of Clinical Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom.
Alex RichterInstitute of Cancer and Genomic Science, College of Medical and Dental Science, University of Birmingham, Birmingham, United Kingdom.
Lance TurtleNIHR Health Protection Research Unit in Emerging and Zoonotic Infections, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Thushan I de SilvaDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.
Miles W CarrollWellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Centre for Human Genetics · GBUniversity of Oxford · GBSheffield Teaching Hospitals NHS Foundation Trust · GBUniversity of Sheffield · GBMahidol Oxford Tropical Medicine Research Unit · THMedawar Building for Pathogen Research · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBUniversity of Birmingham · GBUniversity of Liverpool · GB

Funding

Wellcome Trust 109965/Z/15/ZWellcome Trust 211153/Z/18/Z
6 · The paper itself

Abstract

Two doses of BNT162b2 mRNA vaccine induces a strong systemic SARS-CoV-2 specific humoral response. However, SARS-CoV-2 airborne transmission makes mucosal immune response a crucial first line of defense. Therefore, we characterized SARS-CoV-2-specific IgG responses induced by BNT162b2 vaccine, as well as IgG responses to other pathogenic and seasonal human coronaviruses in oral fluid and plasma from 200 UK healthcare workers who were naïve (N=62) or previously infected with SARS-CoV-2 (N=138) using a pan-coronavirus multiplex binding immunoassay (Meso Scale Discovery

Indexed as

COVID-19Viral VaccinesAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineHumansImmunoglobulin AImmunoglobulin GmRNA VaccinesRNA, MessengerSARS-CoV-2VaccinationVaccines, SyntheticAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralBNT162 VaccineImmunoglobulin AImmunoglobulin GmRNA VaccinesRNA, MessengerVaccines, SyntheticViral VaccinesACE2 inhibitionantibody responsesmRNA vaccinationmucosal immunityneutralizing responsesSARS-CoV-2

Identifiers

PMID36159846
PMCPMC9499336
OpenAlexW4296100791

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.