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Updated: Mar 24, 2026

A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Status of vaccine research and development of vaccines for GBS
1Paediatric Infectious Diseases Research Group, & Vaccine Institute, Institute of Infection & Immunity, St. Georges, University of London, Jenner Wing, Level 2, Room 2.213, London SW17 0RE, United Kingdom.
Insights
Group B Streptococcus (GBS) causes serious neonatal infections. A maternal vaccine could prevent early and late-onset GBS disease, offering a better solution than current antibiotic strategies.
Area of Science:
- Neonatal infectious diseases
- Vaccinology
- Microbiology
Background:
- Streptococcus agalactiae (GBS) is a primary cause of neonatal sepsis and meningitis globally.
- Intrapartum antibiotic prophylaxis (IAP) reduces early-onset GBS but not late-onset disease (LOD).
- The burden of GBS in low/middle-income countries, particularly Southern Africa, is significant and potentially underestimated.
Purpose of the Study:
- To highlight the limitations of current GBS prevention strategies.
- To advocate for the development and implementation of a maternal GBS vaccine.
- To emphasize the potential of vaccination to address both early and late-onset GBS infections in all settings.
Main Methods:
- Review of existing literature on GBS epidemiology and prevention.
- Analysis of the efficacy and limitations of intrapartum antibiotic strategies.
- Discussion of the potential impact and cost-effectiveness of a maternal GBS vaccine.
Main Results:
- IAP strategies are ineffective against late-onset GBS infections.
- Rapidly fulminating GBS cases can be missed, leading to underestimation of disease burden.
- Maternal vaccination presents a promising and potentially cost-effective solution for GBS prevention.
Conclusions:
- A maternal GBS vaccine is a superior strategy for preventing neonatal sepsis and meningitis compared to current IAP.
- Vaccination could provide a comprehensive solution for both early and late-onset GBS disease across diverse healthcare settings.
- Current vaccine development includes CPS-protein conjugate and protein-based candidates, with some in clinical trials.
Abstract:
Streptococcus agalactiae (group B streptococcus (GBS)) is the leading cause of neonatal sepsis and meningitis in many countries. Intrapartum antibiotic strategies have reduced the incidence of early-onset neonatal GBS in a number of countries but have had no impact on late onset GBS infection (LOD). In low/middle income settings, the disease burden remains uncertain although in several countries of Southern Africa appears comparable to or higher than that of high-income countries. As disease may be rapidly fulminating cases can be missed before appropriate samples are obtained and this may lead to underestimation of the true burden. Given the rapid onset and progression within hours of birth as well as the deficiencies in IAP strategies and absence of a solution for preventing LOD, it is clear that administration of a suitable vaccine in pregnancy could provide a better solution in all settings; it should also be cost effective. The current leading vaccine candidates are CPS-protein conjugate vaccines but protein-based vaccines are also in development and one has recently commenced clinical trials.
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