Evidence map›Paper›PMID 38764069›Full record

ArticleMalaria journal2024

IgG and IgM responses to the Plasmodium falciparum asexual stage antigens reflect respectively protection against malaria during pregnancy and infanthood.

Mahugnon L Erasme Gbaguidi, Rafiou Adamou, Sofie Edslev, Anita Hansen, Nadia D Domingo, Celia Dechavanne, Achille Massougbodji, André Garcia, Michael Theisen, Jacqueline Milet and 2 more

Abstract read
In one paragraph

Article in Malaria journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Current update on malaria in pregnancy: a systematic review.Tropical diseases, travel medicine and vaccines · 2025
    Review
  2. Antiplasmodial Activity of ProbioticJournal of tropical medicine · 2024
    Article
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

12 authors.

Mahugnon L Erasme Gbaguidi *Division of Clinical Immunology, Department of Medicine, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
Rafiou Adamou *IRD, MERIT, Université Paris Cité, 75006, Paris, France.
Sofie EdslevInstitut de Recherche Clinique du Bénin, Abomey-Calavi, Benin.
Anita HansenInstitut de Recherche Clinique du Bénin, Abomey-Calavi, Benin.
Nadia D DomingoCentre d'Etude Et de Recherche Sur Les Pathologies Associées À La Grossesse Et À L'Enfance, Cotonou, Bénin.
Celia DechavanneIRD, MERIT, Université Paris Cité, 75006, Paris, France.
Achille MassougbodjiInstitut de Recherche Clinique du Bénin, Abomey-Calavi, Benin.
André GarciaIRD, MERIT, Université Paris Cité, 75006, Paris, France.
Michael TheisenCentre for Medical Parasitology at Department of International Health, Immunology and Microbiology, University of Copenhagen, Rigshospitalet, Copenhagen, Denmark.
Jacqueline MiletIRD, MERIT, Université Paris Cité, 75006, Paris, France.
Eduardo A Donadi *Division of Clinical Immunology, Department of Medicine, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
David Courtin *IRD, MERIT, Université Paris Cité, 75006, Paris, France. David.Courtin@ird.fr.

Funding

Agence Nationale de la Recherche Project ANR- 2010-PRSP-012 001 - TOLIMMUNPAL
6 · The paper itself

Abstract

backgroundPlasmodium falciparum malaria is a public health issue mostly seen in tropical countries. Until now, there is no effective malaria vaccine against antigens specific to the blood-stage of P. falciparum infection. Because the pathogenesis of malarial disease results from blood-stage infection, it is essential to identify the most promising blood-stage vaccine candidate antigens under natural exposure to malaria infection.

methodsA cohort of 400 pregnant women and their infants was implemented in South Benin. An active and passive protocol of malaria surveillance was established during pregnancy and infancy to precisely ascertain malaria infections during the follow-up. Twenty-eight antibody (Ab) responses specific to seven malaria candidate vaccine antigens were repeatedly quantified during pregnancy (3 time points) and infancy (6 time points) in order to study the Ab kinetics and their protective role. Abs were quantified by ELISA and logistic, linear and cox-proportional hazard model were performed to analyse the associations between Ab responses and protection against malaria in mothers and infants, taking into account socio-economic factors and for infants an environmental risk of exposure.

resultsThe levels of IgM against MSP1, MSP2 and MSP3 showed an early protective response against the onset of symptomatic malaria infections starting from the 18th month of life, whereas no association was found for IgG responses during infancy. In women, some IgG responses tend to be associated with a protection against malaria risk along pregnancy and at delivery, among them IgG3 against GLURP-R0 and IgG2 against MSP1.

conclusionThe main finding suggests that IgM should be considered in vaccine designs during infanthood. Investigation of the functional role played by IgM in malaria protection needs further attention.

Indexed as

Antibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GImmunoglobulin MMalaria, FalciparumPlasmodium falciparumAdultBeninCohort StudiesEnzyme-Linked Immunosorbent AssayFemaleHumansInfantInfant, NewbornPregnancyPregnancy Complications, ParasiticAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GImmunoglobulin MAsexual stageIgGIgMInfancyPlasmodium falciparumPregnancy

Identifiers

PMID38764069
PMCPMC11103834

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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.