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Updated: Feb 22, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Maternal immunization against group B Streptococcus: Immune correlates, microbiome trade-offs, and global
Taruna Ikrar1, Wachyudi Muchsin1, Alfi Sophian1
1The Indonesian Food and Drug Authority. Jl. Percetakan Negara, No. 23, Jakarta, Pusat, 10560, Indonesia.
Insights
Maternal vaccines offer a promising strategy to prevent Group B Streptococcus (GBS) disease, complementing antibiotic prophylaxis. This review explores immune responses, microbiome impacts, and implementation challenges for global GBS vaccine deployment.
Area of Science:
- Immunology
- Microbiology
- Global Health
Background:
- Group B Streptococcus (GBS) is a major cause of neonatal sepsis, meningitis, and stillbirth globally.
- Intrapartum antibiotic prophylaxis (IAP) reduces early-onset GBS but doesn't prevent late-onset disease, maternal colonization, or stillbirths, and faces implementation hurdles in low- and middle-income countries (LMICs).
Purpose of the Study:
- To critically examine maternal GBS vaccine development progress.
- To integrate immunological, biological, and implementation factors for future vaccine impact.
- To inform vaccine evaluation, regulation, and policy for global deployment.
Main Methods:
- Review of current progress in maternal GBS vaccine development.
- Integration of immune correlates of protection, microbiome-related trade-offs of IAP, and global implementation challenges.
- Analysis of operational and policy considerations for vaccine introduction in LMICs.
Main Results:
- Advances and uncertainties exist in defining immune correlates for regulatory approval.
- Emerging evidence suggests microbiome perturbations from peripartum antibiotics, though clinical significance is uncertain.
- Operational and policy considerations for LMIC vaccine introduction are analyzed.
Conclusions:
- Maternal vaccination is a promising complementary strategy for equitable GBS disease prevention.
- An integrated framework is needed to guide evaluation and deployment of maternal GBS vaccines.
- Addressing implementation challenges is crucial for global impact, especially in LMICs.
Abstract:
Group B Streptococcus (GBS) remains a leading cause of neonatal sepsis, meningitis, stillbirth, and long-term neurodevelopmental impairment worldwide. Although intrapartum antibiotic prophylaxis (IAP) has substantially reduced early-onset GBS disease in high-income settings and remains an effective and evidence-based intervention, it does not prevent late-onset disease, maternal colonization, or GBS-associated stillbirths, and its implementation is challenging in many low- and middle-income countries (LMICs). Maternal vaccination has therefore emerged as a promising complementary strategy to achieve broader, more equitable prevention of GBS disease. This review critically examines current progress in maternal GBS vaccine development by integrating three interrelated dimensions that will shape future vaccine impact: immune correlates of protection, microbiome-related trade-offs of existing antibiotic-based prevention strategies, and global implementation challenges. We highlight recent advances and remaining uncertainties in defining serological and functional immune correlates required for regulatory decision-making, discuss emerging evidence on microbiome perturbations associated with peripartum antibiotic exposure while emphasizing their currently uncertain clinical significance, and analyze operational and policy considerations relevant to vaccine introduction in LMICs. By moving beyond descriptive summaries of the vaccine development pipeline, this review provides an integrated immunological, biological, and implementation-focused framework to inform vaccine evaluation, regulatory pathways, and policy decisions as maternal GBS vaccines approach licensure and global deployment.
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