Target intelligence / Profile preview

Group B Streptococcus capsular polysaccharide (serotypes Ia, Ib, II, III, IV, V) (GBS CPS)

Target
GBS CPS
Molecular classification
Polysaccharide, Bacterial surface antigen, Virulence factor
01

Overview

Group B Streptococcus (GBS), or Streptococcus agalactiae, is a leading cause of life-threatening neonatal infections, including sepsis, pneumonia, and meningitis (Madhi et al., 2023, NEJM). The capsular polysaccharide (CPS) is the primary virulence factor of GBS, forming a protective layer that inhibits opsonophagocytosis by the host's immune system (Paoletti & Kasper, 2019, Vaccine). While ten GBS serotypes have been identified, six specific serotypes—Ia, Ib, II, III, IV, and V—account for approximately 98% of invasive GBS disease cases globally (Pfizer, 2023). The IVT GBS-06 (GBS6) vaccine is a hexavalent conjugate vaccine designed to target these six serotypes by linking the polysaccharides to a CRM197 carrier protein. This conjugation converts the polysaccharides into T-cell dependent antigens, stimulating the production of high-affinity IgG antibodies in pregnant women. These antibodies are then transferred across the placenta to the fetus, providing passive protection to the newborn during the period of highest vulnerability (Absba et al., 2022, Frontiers in Immunology). Clinical efficacy is measured by the ability of these antibodies to induce opsonophagocytic killing of the bacteria. This target is critical for reducing the global burden of neonatal GBS disease, for which no vaccine is currently licensed.

Other names
Streptococcus agalactiae capsular polysaccharideGBS capsular polysaccharideGBS6 antigensHexavalent GBS polysaccharidePF-06760805 antigens
02

Mechanism of action

Induction of serotype-specific opsonophagocytic antibodies (IgG) that facilitate bacterial clearance via the host immune system and provide passive immunity to neonates through transplacental transfer (Madhi et al., 2023, NEJM).

03

Biological functions

Bacterial virulenceImmune evasionInhibition of opsonophagocytosis
04

Disease associations

InfectionNeonatal sepsisNeonatal meningitisPneumoniaInvasive Group B Streptococcus disease
05

Safety considerations

Injection site reactionsSystemic reactogenicity (fever, headache)Potential for serotype replacement
06

Interacting drugs

GBS6

1 more in the full profile.

07

Biomarkers

Serotype-specific IgG concentrationOpsonophagocytic activity (OPA) titersMaternal-to-infant antibody transfer ratio

Beyond the preview

Go deeper on Group B Streptococcus capsular polysaccharide (serotypes Ia, Ib, II, III, IV, V) (GBS CPS).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Group B Streptococcus capsular polysaccharide (serotypes Ia, Ib, II, III, IV, V) (GBS CPS).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call