A Novel Hexavalent Capsular Polysaccharide Conjugate Vaccine (GBS6) for the Prevention of Neonatal Group B Streptococcal Infections by Maternal Immunization
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Updated: Jan 29, 2026

Intranasal Immunization and Milk Collection in Studies of Maternal Immunization in New Zealand White Rabbits Oryctolagus cuniculus
Published on: July 31, 2021
Ed T Buurman1, Yekaterina Timofeyeva1, Jianxin Gu1
1Vaccine Research and Development, Pfizer, Pearl River, New York.
Insights
A new Group B Streptococcus (GBS) vaccine (GBS6) shows promise for protecting newborns. Maternal vaccination with GBS6 induced protective antibodies, safeguarding infants from GBS infection.
Area of Science:
- Bacteriology
- Immunology
- Vaccine Development
Background:
- Group B Streptococcus (GBS) poses severe risks to newborns, causing lifelong disabilities or death.
- Maternal vaccination offers a potential strategy to protect infants from early-onset, late-onset, and maternal GBS complications.
Purpose of the Study:
- To develop and evaluate a novel GBS vaccine (GBS6) for maternal immunization.
- To assess the immunogenicity and protective efficacy of GBS6 in preclinical models.
Main Methods:
- GBS6 conjugate vaccine synthesized using GBS capsular polysaccharides and CRM197.
- Immunogenicity assessed via IgG antibody levels and opsonophagocytic activity in mice and macaques.
- Efficacy evaluated through protection of pups from lethal GBS challenge after maternal immunization.
Main Results:
- GBS6 conjugates were immunogenic, eliciting robust IgG responses and opsonophagocytic activity in animal models.
- Active maternal immunization with GBS6 conferred serotype-specific protection to offspring against lethal GBS challenge.
- Passive transfer of anticapsular polysaccharide IgG antibodies confirmed their sufficiency for protection.
Conclusions:
- GBS6 vaccine demonstrates immunogenicity and efficacy in preclinical studies.
- Findings support the clinical investigation of maternal GBS6 vaccination for infant GBS disease prevention.
Background:
Group B streptococcus (GBS) causes serious diseases in newborn infants, often resulting in lifelong neurologic impairments or death. Prophylactic vaccination of pregnant women prior to delivery could provide comprehensive protection, as early onset and late-onset disease and maternal complications potentially could be addressed.
Methods:
Capsular polysaccharide conjugate vaccine GBS6 was designed using surveillance data yielded by whole-genome sequencing of a global collection of recently recovered GBS isolates responsible for invasive neonatal GBS disease. Capsular polysaccharides were isolated, oxidized using sodium periodate, and conjugated to CRM197 by reductive amination in dimethyl sulfoxide. Immune responses in mice and rhesus macaques were measured in a multiplex Luminex immunoglobulin G (IgG) assay and opsonophagocytic activity assays.
Results:
The optimized conjugates were immunogenic, alone and in combination, in mice and rhesus macaques, inducing IgG antibodies that mediated opsonophagocytic killing. Active immunization of murine dams with GBS6 prior to mating resulted in serotype-specific protection of pups from a lethal challenge with GBS. Protection following passive administration of serotype-specific IgG monoclonal antibodies to dams demonstrated conclusively that anticapsular polysaccharide IgG alone is sufficient for protection.
Conclusions:
The findings support the ongoing clinical evaluation of maternal GBS6 vaccination as a potential alternative method to prevent GBS disease in infants.
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