Evidence map›Paper›PMID 42286508›Full record

ArticleBMC infectious diseases2026

Maternal cytokine profile and anti-bacterial specific antibody response associated with neonatal infection by E. coli and K. pneumoniae.

Azeddine Chakroun, Narjis Amar, Hanane Ben-Taleb, Karima Mohtadi, Amine Lamrissi, Amal Badre, Norddine Habti, Hanane Salih Alj, Rachid Saïle, Mustapha Chamekh

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. 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
–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

1 citing paper in PubMed.

  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

10 authors.

Azeddine Chakroun *Laboratory of Pediatric Research, Inflammation Unit, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Narjis Amar *Laboratory of Pediatric Research, Inflammation Unit, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Hanane Ben-TalebLaboratory of Pediatric Research, Inflammation Unit, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Karima MohtadiLaboratory of Biology and Health, Research Center of Biotechnology and Health, Faculty of Sciences Ben Msik, Hassan II University of Casablanca, Casablanca, Morocco.
Amine LamrissiGynecology Obstetric Department, Faculty of Medicine and Pharmacy of Casablanca, Children's Hospital A. Harouchi, CHU Ibn Rochd, Hassan II University of Casablanca, Casablanca, Morocco.
Amal BadreNeonatal Reanimation Department (P4), CHU Ibn Rochd, Faculty of Medicine and Pharmacy of Casablanca, Children's Hospital A. Harouchi, Hassan II University of Casablanca, Casablanca, Morocco.
Norddine HabtiLaboratory of Hematology, Genetic and Cellular Engineering, Faculty of Medicine and Pharmacy of Casablanca, Hassan II University of Casablanca, Casablanca, Morocco.
Hanane Salih AljLaboratory of Biology and Health, Research Center of Biotechnology and Health, Faculty of Sciences Ben Msik, Hassan II University of Casablanca, Casablanca, Morocco.
Rachid SaïleLaboratory of Biology and Health, Research Center of Biotechnology and Health, Faculty of Sciences Ben Msik, Hassan II University of Casablanca, Casablanca, Morocco.
Mustapha ChamekhLaboratory of Pediatric Research, Inflammation Unit, Faculty of Medicine, Université Libre de Bruxelles (ULB), Brussels, Belgium. mostafa.chamekh@ulb.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe transmission of pathogenic Gram-negative bacteria such as Escherichia coli and Klebsiella pneumoniae from mother to child during pregnancy contributes significantly to neonatal morbidity and mortality, particularly in low and middle-income countries. Identifying maternal risk factors associated with vertical transmission is crucial. This prospective study aimed to investigate the maternal cytokine profile and anti-LPS-specific antibodies in pregnant mothers with positive cultures for E. coli and K. pneumoniae, exploring their potential association with neonatal invasive disease.

methodsThis prospective study examined groups of pregnant women with a positive culture for E. coli or K. pneumoniae, who had or had not given birth to newborns with invasive diseases. A group of age-matched mothers negative for E coli and K. pneumoniae was used as a control. A panel of circulating inflammatory cytokines was measured in mother-infant dyads using Luminex multiplex assays or ELISA in maternal and cord blood, as well as in the supernatants of blood leucocytes stimulated with TLR4 and TLR1/2 ligands. The serum levels of specific IgG anti-LPS E. coli and anti-LPS K. pneumoniae were quantified using ELISA.

resultsMothers with a positive culture for E. coli and K. pneumoniae and their newborns exhibited elevated plasma levels of IL-6, IL-8, and TNF-α compared to healthy mothers and their newborns. Similar results were observed for IL-6 and TNF-α when blood leucocytes were stimulated by TLR4 and TLR1/2 ligands. Mothers who gave birth to newborns with severe infectious diseases had higher IL-6 levels and lower specific IgG anti-LPS E. coli or anti-LPS K. pneumoniae levels compared to those with healthy newborns. Receiver operating characteristic (ROC) analysis demonstrated a strong association between maternal IL-6 and specific IgG levels and perinatal bacterial transmission.

conclusionPregnant women with positive cultures for E. coli or K. pneumoniae, as well as higher plasma levels of IL-6 and lower levels of specific anti-bacterial IgG, are at increased risk of perinatal bacterial transmission. This data could help improve the monitoring of mother-child dyads and optimize prenatal care.

trial registrationClinical trial number: not applicable.

Indexed as

Antibodies, BacterialCytokinesEscherichia coli InfectionsKlebsiella InfectionsPregnancy Complications, InfectiousAdultEscherichia coliFemaleHumansImmunoglobulin GInfant, NewbornInfectious Disease Transmission, VerticalInterleukin-6Klebsiella pneumoniaePregnancyProspective StudiesAntibodies, BacterialCytokinesImmunoglobulin GInterleukin-6Antibody responseE. coliInflammatory cytokinesK. pneumoniaeMaternal-fetal infection

Identifiers

PMID42286508
PMCPMC13491783

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LicenceCC BY-NC-ND
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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.