Evidence map›Paper›PMID 40597729›Full record

Observational studyBMC infectious diseases2025

Placental transfer of SARS-CoV-2 antibodies in mother-neonate pairs: a prospective nested cohort study.

Alex G Mugo, Angela Koech, Liberty Cantrell, Moses Mukhanya, Isaac Mwaniki, Joseph Mutunga, Merryn Voysey, Rachel Craik, Peter von Dadelszen, Kirsty Le Doare and 4 more

Abstract readObservational Study
In one paragraph

Observational study in BMC infectious diseases, 2025. 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

14 authors.

Alex G MugoCentre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya. alex.mugo@aku.edu.
Angela KoechCentre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya.
Liberty CantrellOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
Moses MukhanyaCentre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya.
Isaac MwanikiCentre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya.
Joseph MutungaCentre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya.
Merryn VoyseyOxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
Rachel CraikDepartment of Women and Children's Health, King's College London, London, UK.
Peter von DadelszenDepartment of Women and Children's Health, King's College London, London, UK.
Kirsty Le DoareCentre for Neonatal and Paediatric Infection, Maternal and Neonatal Vaccinology Research Group, St. George's School of Health and Medical Sciences, City St George's, University of London, London, UK.
Marleen TemmermanCentre of Excellence in Women and Child Health, Aga Khan University, Nairobi, Kenya.
Geoffrey OmuseDepartment of Pathology, Aga Khan University, Nairobi, Kenya.
periCOVID-Africa
PRECISE Network

Funding

United Kingdom Research and Innovation Grand Challenges Research Fund GROW Award scheme MR/P027938/1
6 · The paper itself

Abstract

backgroundNewborns depend on the transfer of IgG across the placenta to acquire protection against pathogens. We assessed the placental transfer of SARS-CoV-2 antibodies, primarily derived from infection, from seropositive pregnant women enrolled in a pregnancy cohort in Kilifi, Kenya.

methodsThe study was nested within a prospective observational multi-country cohort study. All available paired maternal delivery and cord blood samples were selected. Maternal sera were tested for SARS-CoV-2 receptor binding domain (RBD) IgM/IgG total antibodies using the Wantai assay. For positive samples, maternal and corresponding cord blood samples were tested for SARS-CoV-2 IgG antibodies against the spike (anti-spike) and nucleocapsid proteins (anti-NCP) using ELISA kits from Euroimmun.

resultsA total of 492 (56.1%) out of 877 maternal delivery samples were positive for RBD IgM/IgG total antibodies. Of these, 416 (84.6%) were seropositive for either anti-NCP IgG, anti-spike IgG antibodies or both. A total of 412 out of 496 (83%) cord blood samples tested positive for either anti-NCP or anti-spike antibodies. The geometric mean ratio was 1.04 (95% CI: 0.90, 1.21), indicating no significant difference between the anti-spike IgG concentration in cord and maternal blood samples. The log-transformed maternal and cord blood anti-spike IgG concentrations showed a weak positive correlation (r = 0.364, n = 496, p < 0.001). No maternal or neonatal factors were associated with the anti-spike IgG placental transfer ratio.

conclusionPlacental transfer of SARS-CoV-2 antibodies was evident in a population of pregnant women whose immunity was primarily derived from infection given the low SARS-CoV-2 vaccine coverage in the study area. The positive correlation between maternal and cord blood anti-spike concentrations suggests that interventions that increase maternal antibody concentrations such as vaccination may increase passive immunity and protection against severe COVID-19 disease in neonates.

Indexed as

Antibodies, ViralCOVID-19Maternal-Fetal ExchangePlacentaPregnancy Complications, InfectiousSARS-CoV-2AdultCoronavirus Nucleocapsid ProteinsFemaleFetal BloodHumansImmunity, Maternally-AcquiredImmunoglobulin GImmunoglobulin MInfant, NewbornKenyaAntibodies, ViralCoronavirus Nucleocapsid ProteinsImmunoglobulin GImmunoglobulin MSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19EfficiencyPlacental transferSARS-CoV-2 antibodiesSeropositivity

Identifiers

PMID40597729
PMCPMC12217198

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.