A1 Refereed original research article in a scientific journal

Association between anti-capsular IgG levels at birth and risk of invasive group B streptococcus disease in Finnish newborns : a retrospective case–control study




AuthorsSaukkoriipi Annika, Silmon de Monerri Natalie C, Toropainen Maija, Lindholm Laura, Veijola Riitta, Toppari Jorma, Knip Mikael, Radley David, Gomme Emily, Jongihlati Babalwa, Anderson Annaliesa S, Palmu Arto A, Simon Raphael

PublisherElsevier

Publication year2024

JournalLancet microbe

Journal name in sourceThe Lancet Microbe

Volume5

Issue7

First page 689

Last page696

ISSN2666-5247

eISSN2666-5247

DOIhttps://doi.org/10.1016/S2666-5247(24)00038-7

Web address https://doi.org/10.1016/S2666-5247(24)00038-7

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/393366993


Abstract

Background: Group B streptococcus is a major cause of neonatal disease. Natural history studies have linked maternally transferred anti-group B streptococcus capsular polysaccharide antibodies with protection against infant group B streptococcus disease. Previous studies of capsular polysaccharide antibody concentration in European populations have used maternal (not infant) sera and a non-standardised assay. This study aimed to evaluate anti-capsular polysaccharide IgG concentrations associated with protection against invasive group B streptococcus disease in Finnish infants.

Methods: In this retrospective case-control study, we used cord sera from the Finnish DIPP study repository, which was obtained between Jan 1, 1995, and Dec 31, 2017. We included infants aged 6 months or younger with group B streptococcus infection (cases) and healthy infants (controls). We enrolled infants with invasive neonatal group B streptococcus (55 cases) and matched controls (229 controls) aged 6 months or younger after identification from Finnish health registers. We measured anti-capsular polysaccharide IgG (serotypes Ia-V) concentration using a standardised immunoassay and we estimated its relationship to disease risk using a Bayesian model. We used the derived risk-concentration curve to predict potential efficacy of six-valent group B streptococcus capsular polysaccharide vaccine (GBS6) based on previously reported immunogenicity data.

Findings: Most (32 [58%] of 55 cases) group B streptococcus cases were due to serotype III and anti-serotype III streptococcus capsular IgG concentrations were higher in serotype III-matched controls than in cases (p<0·001). 0·120-0·266 μg/mL serotype III-specific IgG was estimated to confer 75-90% risk reduction against serotype III disease. A universal risk-concentration curve, aggregating results across all six serotypes, yielded similar results. Application of this curve to GBS6 immunogenicity data predicted maternal immunisation to be more than 80% efficacious for prevention of infant group B streptococcus disease.

Interpretation: Higher neonatal anti-capsular polysaccharide serum IgG concentration at birth correlated with reduced risk of infant group B streptococcus disease in Finland. Based on these results, a maternal group B streptococcus capsular conjugate vaccine currently in development is predicted to be efficacious.


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Funding information in the publication
Funding: Pfizer.


Last updated on 2025-06-03 at 15:36