Evidence map›Paper›PMID 32027020›Full record

Trial reportClinical and experimental immunology2020

IgG antibody response against Plasmodium falciparum aminopeptidase 1 antigen in Gabonese children living in Makokou and Franceville.

S L Oyegue-Liabagui, R-K Imboumy-Limoukou, C L Kouna, F Bangueboussa, M Schmitt, I Florent, J B Lekana-Douki

Open access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Clinical and experimental immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 5 institutions in 2 countries.

S L Oyegue-LiabaguiLaboratoire de Recherches en Immunologie, Parasitologie et Microbiologie, Ecole Doctorale Régionale d'Afrique Centrale en Infectiologie Tropicale (ECODRAC), Université des Sciences et Techniques de Masuku, Franceville, Gabon.ORCID 0000-0002-1689-2459
R-K Imboumy-LimoukouUnité d'Evolution Epidémiologie et Résistances Parasitaires (UNEEREP), Centre International de Recherches Médicales de Franceville (CIRMF), Franceville, Gabon.
C L KounaUnité d'Evolution Epidémiologie et Résistances Parasitaires (UNEEREP), Centre International de Recherches Médicales de Franceville (CIRMF), Franceville, Gabon.
F BangueboussaLaboratoire de Recherches en Immunologie, Parasitologie et Microbiologie, Ecole Doctorale Régionale d'Afrique Centrale en Infectiologie Tropicale (ECODRAC), Université des Sciences et Techniques de Masuku, Franceville, Gabon.
M SchmittUniversité de Haute-Alsace, Université de Strasbourg, Mulhouse, France.
I FlorentMolécules de Communication et Adaptation des Microorganismes (MCAM, UMR 7245), Muséum National d'Histoire Naturelle, Paris, France.
J B Lekana-DoukiUnité d'Evolution Epidémiologie et Résistances Parasitaires (UNEEREP), Centre International de Recherches Médicales de Franceville (CIRMF), Franceville, Gabon.
Centre International de Recherches Médicales de Franceville · GAMolécules de Communication et Adaptation des Micro-organismes · FRUniversité de Haute-Alsace · FRUniversité des Sciences de la Santé · GAUniversité des Sciences et Techniques de Masuku · GA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The search for novel chemical classes of anti-malarial compounds to cope with the current state of chemoresistance of malaria parasites has led to the identification of Plasmodium falciparum aminopeptidase 1 (PfA-M1) as a new therapeutic target. PfA-M1, known to be involved in the hemoglobin digestion cascade which helps to provide most of the amino acids necessary to the parasite's metabolism, is currently considered as a promising target for anti-malarial chemotherapy. However, its immunogenic properties have not yet been tested in the Gabonese population. In Gabon, the prevalence of malaria remains three times higher in semi-urban areas (60·12%) than in urban areas (17·06%). We show that malaria-specific PfA-M1 antibodies are present in children and increase with the level of infection. Children living in semi-urban areas have higher anti-PfA-M1 antibody titers (0·14 ± 0·02 AU) than those living in urban areas (0·08 ± 0·02 AU, P = 0·03), and their antibody titers increase with age (P < 0·0001). Moreover, anti-PfA-M1 antibody titers decrease in children with hyperparasitemia (0·027 ± 0·055 AU) but they remain high in children with low parasite density (0·21 ± 0·034 AU, P = 0·034). In conclusion, our results suggest that malaria-specific PfA-M1 antibodies may play an important role in the immune response of the host against P. falciparum in Gabonese children. Further studies on the role of PfA-M1 during anemia are needed.

Indexed as

AdolescentAminopeptidasesAntibodies, ProtozoanAntigens, ProtozoanChildChild, PreschoolFemaleGabonHumansImmunoglobulin GInfantInfant, NewbornMalaria, FalciparumMalePlasmodium falciparumProtozoan ProteinsAminopeptidasesAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GProtozoan ProteinsantibodyGabonhumoral immunitymalaria infectionPlasmodium falciparum aminopeptidase 1 (PfA-M1)

Identifiers

PMID32027020
PMCPMC7232005
OpenAlexW3004738795

What OpenQuestion holds

Textmetadata
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.