[3] Brigham & Womens Hosp, Channing Lab, Dept Med, Boston, MA USA
[4] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA USA
来源:
JOURNAL OF INFECTIOUS DISEASES
|
2000年
/
182卷
/
04期
关键词:
D O I:
10.1086/315839
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
An estimated 15% of invasive group B streptococcal (GBS) disease is caused by type II capsular polysaccharide (II CPS), In developing a pentavalent vaccine for the prevention of GBS infections, individual GBS CPSs have been coupled to tetanus toroid (TT) to prepare vaccines with enhanced immunogenicity, Type II GBS (GBS II) vaccine was created by direct, covalent coupling of IT CPS to TT by reductive amination. In 2 clinical trials, 75 healthy nonpregnant women 18-45 years old were randomized to receive II CPS-TT (II-TT) conjugate (dose range, 3.6-57 mu g of CPS component) or uncoupled II CPS vaccine. Both vaccines were well tolerated, II CPS-specific IgG serum concentrations (as well as IgM and IgA) peaked 2 weeks after immunization, being significantly higher in recipients of conjugated vaccine than in recipients of uncoupled CPS, Immunological responses to conjugate were dose dependent and correlated with opsonophagocytosis in vitro. These results support inclusion of II-TT conjugate when preparing a multivalent GBS vaccine.