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

Saukkoriipi 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

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

Saukkoriipi 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
Katso/Avaa
1-s2.0-S2666524724000387-main.pdf (302.2Kb)
Lataukset: 

Elsevier
doi:10.1016/S2666-5247(24)00038-7
URI
https://doi.org/10.1016/S2666-5247(24)00038-7
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082786035
Tiivistelmä

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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