Evidence map›Paper›PMID 39692506›Full record

ArticleThe Journal of infectious diseases2025

Diversity in Naturally Acquired Immunity to Group B Streptococcus: A Comparative Study of Women From Bangladesh, Malawi, and the United Kingdom.

Shadia Khandaker, Shilpee Sharma, Tom Hall, Suzanna Lim, Janne Lehtonen, Stephanie Leung, Zabed Bin Ahmed, Andrew Gorringe, Samir K Saha, Arnaud Marchant and 3 more

Abstract readComparative Study
In one paragraph

Article in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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

13 authors.

Shadia KhandakerDepartment of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0001-5084-9772
Shilpee SharmaEuropean Plotkin Institute for Vaccinology, ULB Centre for Research in Immunology, Université libre de Bruxelles, Brussels, Belgium.ORCID 0000-0003-4645-9442
Tom HallCentre for Neonatal and Paediatric Infection, Institute of Infection and Immunity, St George's, University of London, London, United Kingdom.ORCID 0000-0002-9001-6684
Suzanna LimCentre for Neonatal and Paediatric Infection, Institute of Infection and Immunity, St George's, University of London, London, United Kingdom.
Janne LehtonenMinervaX ApS, Copenhagen, Denmark.
Stephanie LeungUnited Kingdom Health Security Agency, Salisbury, United Kingdom.ORCID 0000-0002-8880-2977
Zabed Bin AhmedChild Health Research Foundation, Dhaka, Bangladesh.ORCID 0000-0001-5463-4883
Andrew GorringeUnited Kingdom Health Security Agency, Salisbury, United Kingdom.ORCID 0000-0003-2193-7954
Samir K SahaChild Health Research Foundation, Dhaka, Bangladesh.
Arnaud MarchantEuropean Plotkin Institute for Vaccinology, ULB Centre for Research in Immunology, Université libre de Bruxelles, Brussels, Belgium.
Kirsty Le DoareCentre for Neonatal and Paediatric Infection, Institute of Infection and Immunity, St George's, University of London, London, United Kingdom.ORCID 0000-0002-5104-085X
Aras KadiogluDepartment of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, United Kingdom.
Neil FrenchDepartment of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0003-4814-8293

Funding

BBSRC MR/R005990/2Meningitis Research Foundation 0801.0World Health Organization 001
6 · The paper itself

Abstract

backgroundSignificant disparities in group B Streptococcus (GBS) colonization and neonatal disease rates have been documented across different geographic regions. For example, Bangladesh reports notably lower rates as compared with the United Kingdom and Malawi. This study investigates whether this epidemiologic variability correlates with the immune response to GBS in these regions.

methodsQualitative and quantitative analyses of naturally acquired immunoglobulin G (IgG) antibodies against GBS capsular polysaccharide and the Alp protein family were conducted in serum samples from women of childbearing age in the United Kingdom, Bangladesh, and Malawi. The efficacy of these antibodies in clearing vaginal colonization or protecting newborns from GBS infection was assessed with humanized mouse models.

resultsBangladeshi women displayed the highest diversity in serotype distribution, with elevated IgG levels in the serum against GBS capsular polysaccharides Ia, Ib, II, III, IV, and V, as well as Alp family proteins. In contrast, Malawian sera demonstrated the weakest antibody response. Bangladeshi sera also showed heightened IgG-mediated complement deposition, opsonophagocytic killing, and neonatal Fc receptor binding while tested against capsular polysaccharide Ib. In a humanized neonatal Fc receptor mouse model, Bangladeshi sera led to faster clearance of GBS virulent serotype Ib vaginal colonization. Additionally, offspring from dams passively immunized with Bangladeshi sera demonstrated notably increased survival rates.

conclusionsThis study demonstrates significant variability in the immune response to GBS across different geographic regions. These findings underscore the importance of understanding GBS-induced immune response in diverse populations, which may significantly affect vaccine efficacy in these regions.

Indexed as

Antibodies, BacterialStreptococcal InfectionsStreptococcus agalactiaeAdolescentAdultAnimalsBacterial CapsulesBangladeshFemaleHumansImmunoglobulin GInfant, NewbornMalawiMicePolysaccharides, BacterialUnited KingdomAntibodies, BacterialImmunoglobulin GPolysaccharides, BacterialAlp proteinantibody diversitycapsular polysaccharidegroup B Streptococcusmouse model

Identifiers

PMID39692506
PMCPMC11841642

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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.