Evidence map›Paper›PMID 36311736›Full record

ArticleFrontiers in immunology2022

Symptomatology during previous SARS-CoV-2 infection and serostatus before vaccination influence the immunogenicity of BNT162b2 COVID-19 mRNA vaccine.

Sabryna Nantel, Benoîte Bourdin, Kelsey Adams, Julie Carbonneau, Henintsoa Rabezanahary, Marie-Ève Hamelin, Deirdre McCormack, Patrice Savard, Yves Longtin, Matthew P Cheng and 7 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 12 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

17 authors at 7 institutions in 1 country.

Sabryna NantelCytokines and Adaptive Immunity Lab, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Benoîte BourdinCytokines and Adaptive Immunity Lab, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Kelsey AdamsClinical Department of Laboratory Medicine, Infection Prevention and Control, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Julie CarbonneauInfectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Henintsoa RabezanaharyInfectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Marie-Ève HamelinInfectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Deirdre McCormackClinical Department of Laboratory Medicine, Infection Prevention and Control, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Patrice SavardMicrobiology, Infectiology and Immunology Department, Faculty of Medicine, University of Montréal, Montréal, QC, Canada.
Yves LongtinInfectious Diseases Service, Department of Medicine, Jewish General Hospital, Montréal, QC, Canada.
Matthew P ChengBiological and Occupational Risk, Divisions of Infectious Diseases and Medical Microbiology, Departments of Medicine and Laboratory Medicine, McGill University Health Center, Montréal, QC, Canada.
Gaston De SerresCentre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Jacques CorbeilCentre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Vladimir GilcaCentre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Mariana BazInfectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Guy BoivinInfectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Caroline QuachMicrobiology, Infectiology and Immunology Department, Faculty of Medicine, University of Montréal, Montréal, QC, Canada.
Hélène DecaluweCytokines and Adaptive Immunity Lab, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Université Laval · CACentre Hospitalier Universitaire Sainte-Justine · CAUniversité de Montréal · CACentre hospitalier universitaire de Québec · CAInstitut National de Santé Publique du Québec · CAJewish General Hospital · CAMcGill University Health Centre · CA

Funding

Large Scale T Cell Epitope Discovery:Global identification of epitopes derived from Zika (ZIKV), Chikungunya (CHIKV) viruses following natural infection and vaccination75N93019C00065 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI MITCHELL, MAYA · 2019 to 2023
$7.3M
NIAID NIH HHS 75N93019C00065
6 · The paper itself

Abstract

Public health vaccination recommendations for COVID-19 primary series and boosters in previously infected individuals differ worldwide. As infection with SARS-CoV-2 is often asymptomatic, it remains to be determined if vaccine immunogenicity is comparable in all previously infected subjects. This study presents detailed immunological evidence to clarify the requirements for one- or two-dose primary vaccination series for naturally primed individuals. The main objective was to evaluate the immune response to COVID-19 mRNA vaccination to establish the most appropriate vaccination regimen to induce robust immune responses in individuals with prior SARS-CoV-2 infection. The main outcome measure was a functional immunity score (zero to three) before and after vaccination, based on anti-RBD IgG levels, serum capacity to neutralize live virus and IFN-γ secretion capacity in response to SARS-CoV-2 peptide pools. One point was attributed for each of these three functional assays with response above the positivity threshold. The immunity score was compared based on subjects' symptoms at diagnosis and/or serostatus prior to vaccination. None of the naïve participants (n=14) showed a maximal immunity score of three following one dose of vaccine compared to 84% of the previously infected participants (n=55). All recovered individuals who did not have an immunity score of three were seronegative prior to vaccination, and 67% had not reported symptoms resulting from their initial infection. Following one dose of vaccine, their immune responses were comparable to naïve individuals, with significantly weaker responses than individuals who were symptomatic during infection. These results indicate that the absence of symptoms during initial infection and negative serostatus prior to vaccination predict the strength of immune responses to COVID-19 mRNA vaccine. Altogether, these findings highlight the importance of administering the complete two-dose primary regimen and following boosters of mRNA vaccines to individuals who experienced asymptomatic SARS-CoV-2 infection.

Indexed as

COVID-19Viral VaccinesBNT162 VaccineCOVID-19 VaccinesHumansmRNA VaccinesRNA, MessengerSARS-CoV-2VaccinationBNT162 VaccineCOVID-19 VaccinesmRNA VaccinesRNA, MessengerViral Vaccinesadaptive immune responseCOVID-19hybrid immunitymRNA vaccinationSARS-CoV-2

Identifiers

PMID36311736
PMCPMC9614167
OpenAlexW4306160743

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.