Safety and immunogenicity of a bivalent group B streptococcal conjugate vaccine for serotypes II and III.

To determine whether 2 monovalent group B streptococcus (GBS) serotype II or III capsular polysaccharide (CPS)-tetanus toxoid (TT) conjugate vaccines combined in a single intramuscular dose would elicit immune responses comparable to those of monovalent vaccines, 75 healthy adults were randomized to receive GBS II-TT (3.6 micro g of CPS), GBS III-TT (12.5 micro g of CPS), or a bivalent mixture of GBS II-TT/III-TT vaccine (double-masked design). Vaccines were well tolerated. Four-fold or greater increases in GBS II or III CPS-specific IgG, respectively, were noted in postimmunization serum samples from 80%-90% of bivalent conjugate vaccine recipients, and these responses were similar to those of recipients of GBS II-TT or GBS III-TT monovalent vaccines. Immune serum samples promoted the opsonophagocytic killing of types II and III GBS in vitro. Unexpectedly, some recipients of these vaccines developed cross-reactive antibodies to the structurally similar heterologous polysaccharide. These results support the feasibility of a multivalent vaccine for the 5 prevalent invasive disease-causing GBS CPS serotypes.

[1]  C. Baker,et al.  Group B streptococcal conjugate vaccines , 2003, Archives of disease in childhood.

[2]  D. Eschenbach Prevention of neonatal group B streptococcal infection. , 2002, The New England journal of medicine.

[3]  D. Kasper,et al.  Induction of cross-reactive antibodies by immunization of healthy adults with types Ia and Ib group B streptococcal polysaccharide-tetanus toxoid conjugate vaccines. , 2002, The Journal of infectious diseases.

[4]  D. Kasper,et al.  Effects of Alum Adjuvant or a Booster Dose on Immunogenicity during Clinical Trials of Group B Streptococcal Type III Conjugate Vaccines , 2001, Infection and Immunity.

[5]  J. Eskola,et al.  Cross-reactivity of antibodies to type 6B and 6A polysaccharides of Streptococcus pneumoniae, evoked by pneumococcal conjugate vaccines, in infants. , 2001, The Journal of infectious diseases.

[6]  D. Kasper,et al.  Use of capsular polysaccharide-tetanus toxoid conjugate vaccine for type II group B Streptococcus in healthy women. , 2000, The Journal of infectious diseases.

[7]  R. Platt,et al.  Invasive disease due to group B Streptococcus in pregnant women and neonates from diverse population groups. , 2000, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[8]  A. Schuchat,et al.  Group B streptococcal disease in the era of intrapartum antibiotic prophylaxis. , 2000, The New England journal of medicine.

[9]  G. Lindahl,et al.  Protection against experimental infection with group B streptococcus by immunization with a bivalent protein vaccine. , 1999, Vaccine.

[10]  D. Kasper,et al.  Safety and immunogenicity of capsular polysaccharide-tetanus toxoid conjugate vaccines for group B streptococcal types Ia and Ib. , 1999, The Journal of infectious diseases.

[11]  A. Schuchat,et al.  Serotype distribution of invasive group B streptococcal isolates in Maryland: implications for vaccine formulation. Maryland Emerging Infections Program. , 1998, The Journal of infectious diseases.

[12]  M. Nahm,et al.  Identification of cross-reactive antibodies with low opsonophagocytic activity for Streptococcus pneumoniae. , 1997, The Journal of infectious diseases.

[13]  D. Kasper,et al.  Immune response to type III group B streptococcal polysaccharide-tetanus toxoid conjugate vaccine. , 1996, The Journal of clinical investigation.

[14]  R. Edelman,et al.  Safety and immunogenicity of a tetravalent group B streptococcal polysaccharide vaccine in healthy adults. , 1996, Vaccine.

[15]  D. Kasper,et al.  Quantitative determination of antibodies to type III group B streptococcal polysaccharide. , 1996, The Journal of infectious diseases.

[16]  M. Steinhoff,et al.  The reverse cumulative distribution plot: a graphic method for exploratory analysis of antibody data. , 1995, Pediatrics.

[17]  D. Kasper,et al.  Neonatal mouse protection against infection with multiple group B streptococcal (GBS) serotypes by maternal immunization with a tetravalent GBS polysaccharide-tetanus toxoid conjugate vaccine , 1994, Infection and immunity.

[18]  Gary J. Nabel,et al.  New Generation Vaccines , 1990 .

[19]  D. Kasper,et al.  Immunogenicity in animals of a polysaccharide-protein conjugate vaccine against type III group B Streptococcus. , 1990, The Journal of clinical investigation.

[20]  D. Kasper,et al.  Immunization of Pregnant Women with a Polysaccharide Vaccine of Group B Streptococcus , 1988 .

[21]  D. Kasper,et al.  Structure and immunochemistry of an oligosaccharide repeating unit of the capsular polysaccharide of type III group B Streptococcus. A revised structure for the type III group B streptococcal polysaccharide antigen. , 1987, The Journal of biological chemistry.

[22]  Lee-Jen Wei,et al.  Combining dependent tests with incomplete repeated measurements , 1985 .

[23]  D. Kasper,et al.  Group B streptococcal vaccines. , 1985, Reviews of infectious diseases.

[24]  D. Kasper,et al.  Structural determination of the capsular polysaccharide antigen of type II group B Streptococcus. , 1983, The Journal of biological chemistry.

[25]  D. Kasper,et al.  Influence of preimmunization antibody levels on the specificity of the immune response to related polysaccharide antigens. , 1980, The New England journal of medicine.