Evidence map›Paper›PMID 38156395›Full record

ArticleImmunity, inflammation and disease2023

Mucosal response of inactivated and recombinant COVID-19 vaccines in Congolese individuals.

Freisnel H Mouzinga, Constanze Heinzel, Abel Lissom, Andrea Kreidenweiss, Armel L Batchi-Bouyou, Jacques D Mbama Ntabi, Jean C Djontu, Etienne Ngumbi, Peter G Kremsner, Rolf Fendel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. 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

11 authors at 6 institutions in 5 countries.

Freisnel H MouzingaFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Constanze HeinzelInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Abel LissomFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Andrea KreidenweissInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Armel L Batchi-BouyouFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Jacques D Mbama NtabiFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Jean C DjontuFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Etienne NgumbiFaculté des Sciences et Techniques, Université Marien Ngouabi, Brazzaville, Republic of Congo.
Peter G KremsnerInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Rolf FendelInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Francine NtoumiFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.ORCID 0000-0003-4748-050X
Fondation Congolaise Pour La Recherche Médicale · CGCentre de Recherche Médicales de Lambaréné · GAHarvard University · USMarien Ngouabi University · CGUniversity of Bamenda · CMUniversity of Tübingen · DE

Funding

Bill & Melinda Gates Foundation INV-036514
6 · The paper itself

Abstract

backgroundThe efficacy of immunization against an airborne pathogen depends in part on its ability to induce antibodies at the major entry site of the virus, the mucosa. Recent studies have revealed that mucosal immunity is poorly activated after vaccination with messenger RNA vaccines, thus failing in blocking virus acquisition upon its site of initial exposure. Little information is available about the induction of mucosal immunity by inactivated and recombinant coronavirus disease 2019 (COVID-19) vaccines. This study aims to investigate this topic.

methodsSaliva and plasma samples from 440 healthy Congolese were collected including (1) fully vaccinated 2 month postvaccination with either an inactivated or a recombinant COVID-19 vaccine and (2) nonvaccinated control group. Total anti-severe acute respiratory syndrome coronavirus 2 receptor-binding domain IgG and IgA antibodies were assessed using in-house enzyme-linked immunosorbent assays for both specimens.

findingsAltogether, the positivity of IgG was significantly higher in plasma than in saliva samples both in vaccinated and nonvaccinated control groups. Inversely, IgA positivity was slightly higher in saliva than in plasma of vaccinated group. The overall IgG and IgA levels were respectively over 10

conclusionInactivated and recombinant COVID-19 vaccines in use in the Republic of Congo poorly activated mucosal IgA-mediated antibody response 2 months postvaccination.

Indexed as

COVID-19COVID-19 VaccinesHumansImmunoglobulin AImmunoglobulin GMucous MembraneCOVID-19 VaccinesImmunoglobulin AImmunoglobulin Gantibody levelIgGinactivated and recombinant COVID-19 vaccinesmucosal IgA-mediated antibody

Identifiers

PMID38156395
PMCPMC10751728
OpenAlexW4390277070

What OpenQuestion holds

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LicenceCC BY
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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.