Evidence map›Paper›PMID 42648772›Full record

Trial reportBMJ open2026

Cohort profile: the Entebbe Mother and Baby Study (EMaBS).

Emily L Webb, Bridgious Walusimbi, Ronald Komata, Alison M Elliott, The EMaBS Study Team

Registry-linked trialAbstract readClinical Trial, Phase IClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03681860 (Open Label, Dose Escalation and Age De-escalation for ChAdOx1 85A in Ugandan Adults and Adolescents, Followed by a Phase IIa Randomised, Open-label Trial Among Adolescents Comparing ChAdOx1 85A Prime Followed by MVA 85A Boost Versus BCG Re-vaccination.), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT03681860 phase1 / phase2completednot on this map

Open Label, Dose Escalation and Age De-escalation for ChAdOx1 85A in Ugandan Adults and Adolescents, Followed by a Phase IIa Randomised, Open-label Trial Among Adolescents Comparing ChAdOx1 85A Prime Followed by MVA 85A Boost Versus BCG Re-vaccination.

TypeinterventionalSponsorUniversity of OxfordRan2019 to 2021Enrolled72ConditionsSafety, ImmunogenicityArmsChAdOx185A, MVA85A, BCG
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Emily L WebbMRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda emily.webb@lshtm.ac.uk.ORCID http://orcid.org/0000-0002-4019-7456
Bridgious WalusimbiMRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda.
Ronald KomataMRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda.ORCID http://orcid.org/0009-0008-0975-0728
Alison M ElliottMRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda.ORCID http://orcid.org/0000-0003-2818-9549
The EMaBS Study TeamMRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda.

Funding

Wellcome Trust
6 · The paper itself

Abstract

purposeThe Entebbe Mother and Baby Study (EMaBS) was established in 2001 to test the hypothesis that treating helminth infections during pregnancy and early childhood could improve children's responses to Bacillus Calmette-Guérin (BCG) and other vaccines given in infancy and influence immune responses to other infectious pathogens. Follow-up was subsequently extended to address further research questions and continue to the present day.

participantsTwo thousand five hundred and seven pregnant women were recruited when attending antenatal services at Entebbe General Hospital, Uganda; 2345 resulting live-born children were enrolled into the EMaBS birth cohort. FINDINGS TO DATE: Initial results from EMaBS showed that treating helminths in pregnancy and early childhood was safe and that treatment with albendazole reduced anaemia in mothers with heavy hookworm infections. Maternal anthelminthic treatment had small effects on infant response to tetanus immunisation, but no effect, either beneficial or detrimental on the occurrence of infectious diseases in childhood. However, treatment of helminths during pregnancy resulted in increased rates of eczema in early childhood, although this was not sustained to nine years. Subsequent work in early adolescence found that postnatal weight gain was important in the developmental programming of blood pressure in this population and current and early-life malaria modified blood pressure and lipid levels. We also showed that variation in host genes significantly shapes antibody responses to multiple childhood vaccines, highlighting genetics as a key determinant of vaccine performance. FUTURE PLANS: Cohort 'children' are currently aged 19-22 years, and future plans focus on investigating longer term effects of early-life and childhood exposures. A new round of data collection is ongoing with the aim of determining the impact of early-life exposures on adult non-communicable disease risk. Work determining whether frequent childhood infections lead to specific epigenetic changes implicated in later disease development is also underway. REGISTRATION: The EMaBS began as a randomised controlled trial (ISRCTN32849447). Two further randomised controlled trials have been nested within the cohort: TB042 (NCT03681860) and POPVAC C (ISRCTN10482904).

Indexed as

AlbendazoleAnthelminticsBCG VaccineHelminthiasisPregnancy Complications, ParasiticAdultChild, PreschoolCohort StudiesEczemaFemaleHumansInfantInfant, NewbornMalePregnancyUgandaAlbendazoleAnthelminticsBCG VaccineAfrica South of the SaharaEPIDEMIOLOGIC STUDIESImmunityINFECTIOUS DISEASESLongitudinal studies

Identifiers

PMID42648772
PMCPMC13536125

What OpenQuestion holds

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Registered trials

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.