Immune responses of infants vaccinated with serotype 6B pneumococcal polysaccharide conjugated with tetanus toxoid
dc.contributor.author | Sigurdardottir, S T | |
dc.contributor.author | Vidarsson, G | |
dc.contributor.author | Gudnason, T | |
dc.contributor.author | Kjartansson, S | |
dc.contributor.author | Kristinsson, K G | |
dc.contributor.author | Jonsson, S | |
dc.contributor.author | Valdimarsson, H | |
dc.contributor.author | Schiffman, G | |
dc.contributor.author | Schneerson, R | |
dc.contributor.author | Jonsdottir, I | |
dc.date.accessioned | 2010-09-17T13:49:04Z | |
dc.date.available | 2010-09-17T13:49:04Z | |
dc.date.issued | 1997-07-01 | |
dc.date.submitted | 2010-09-17 | |
dc.identifier.citation | Pediatr. Infect. Dis. J. 1997, 16(7):667-74 | en |
dc.identifier.issn | 0891-3668 | |
dc.identifier.pmid | 9239771 | |
dc.identifier.doi | 10.1097/00006454-199707000-00009 | |
dc.identifier.uri | http://hdl.handle.net/2336/111296 | |
dc.description | To access publisher full text version of this article. Please click on the hyperlink in Additional Links field | en |
dc.description.abstract | BACKGROUND: Streptococcus pneumoniae is a major cause of meningitis, bacteremia, pneumonia and otitis media. Pneumococcal polysaccharides are not immunogenic in infants, but improved immunogenicity of polysaccharide-protein conjugates has been demonstrated. Antibiotic-resistant pneumococci have increased the need for an effective vaccine. OBJECTIVE: To study the safety and immunogenicity of a pneumococcal type 6B polysaccharidetetanus toxoid conjugate (Pn6B-TT) in infants and to assess the function of antibodies. METHODS: Healthy infants were injected, Group A at 3, 4 and 6 months (n = 21) and Group B at 7 and 9 months (n = 19). Booster injection was given at 18 months. Antibodies were measured by enzyme-linked immunosorbent assay and radioimmunoassay, and functional activity was measured by opsonization of radiolabeled pneumococci. Nasopharyngeal cultures were obtained. RESULTS: No significant adverse reactions were observed. Pn6B-IgG (enzyme-linked immunosorbent assay) increased to a geometric mean of 0.62 microgram/ml (P = 0.367, compared with prevaccination titers) in Group A at 7 months and 1.22 micrograms/ml (P < 0.001) in Group B at 10 months. Total Pn6B antibodies (radioimmunoassay) were 44 ng of antibody N/ml (P < 0.053) in Group A and 211 ng of antibody N/ml (P < 0.001) in Group B. A smaller increase in IgM and IgA anti-Pn6B was observed. Reinjection at 18 months elicited booster responses in total and IgG anti-Pn6B; 62% of those in Group A and 79% of those in Group B had > 300 ng of antibody N/ml. Opsonic activity, after initial and booster vaccinations, correlated with Pn6B-antibody titers. Three infants with nasopharyngeal cultures repeatedly positive for serogroup 6 had poor serum IgG responses. CONCLUSION: Our results demonstrate that Pn6B-TT is safe, elicits functional antibodies and memory responses in infants. | |
dc.language.iso | en | en |
dc.publisher | Lippincott Williams & Wilkins Ltd. | en |
dc.relation.url | http://dx.doi.org/10.1097/00006454-199707000-00009 | en |
dc.subject.mesh | Antibodies, Bacterial | en |
dc.subject.mesh | Female | en |
dc.subject.mesh | Humans | en |
dc.subject.mesh | Immunoglobulin A, Secretory | en |
dc.subject.mesh | Infant | en |
dc.subject.mesh | Male | en |
dc.subject.mesh | Nasopharynx | en |
dc.subject.mesh | Phagocytosis | en |
dc.subject.mesh | Polysaccharides, Bacterial | en |
dc.subject.mesh | Saliva | en |
dc.subject.mesh | Streptococcus pneumoniae | en |
dc.subject.mesh | Tetanus Toxoid | en |
dc.subject.mesh | Vaccination | en |
dc.subject.mesh | Vaccines, Conjugate | en |
dc.title | Immune responses of infants vaccinated with serotype 6B pneumococcal polysaccharide conjugated with tetanus toxoid | en |
dc.type | Article | en |
dc.contributor.department | Department of Immunology, National University Hospital, Reykjavik, Iceland. | en |
dc.identifier.journal | Pediatric infectious disease journal | en |
html.description.abstract | BACKGROUND: Streptococcus pneumoniae is a major cause of meningitis, bacteremia, pneumonia and otitis media. Pneumococcal polysaccharides are not immunogenic in infants, but improved immunogenicity of polysaccharide-protein conjugates has been demonstrated. Antibiotic-resistant pneumococci have increased the need for an effective vaccine. OBJECTIVE: To study the safety and immunogenicity of a pneumococcal type 6B polysaccharidetetanus toxoid conjugate (Pn6B-TT) in infants and to assess the function of antibodies. METHODS: Healthy infants were injected, Group A at 3, 4 and 6 months (n = 21) and Group B at 7 and 9 months (n = 19). Booster injection was given at 18 months. Antibodies were measured by enzyme-linked immunosorbent assay and radioimmunoassay, and functional activity was measured by opsonization of radiolabeled pneumococci. Nasopharyngeal cultures were obtained. RESULTS: No significant adverse reactions were observed. Pn6B-IgG (enzyme-linked immunosorbent assay) increased to a geometric mean of 0.62 microgram/ml (P = 0.367, compared with prevaccination titers) in Group A at 7 months and 1.22 micrograms/ml (P < 0.001) in Group B at 10 months. Total Pn6B antibodies (radioimmunoassay) were 44 ng of antibody N/ml (P < 0.053) in Group A and 211 ng of antibody N/ml (P < 0.001) in Group B. A smaller increase in IgM and IgA anti-Pn6B was observed. Reinjection at 18 months elicited booster responses in total and IgG anti-Pn6B; 62% of those in Group A and 79% of those in Group B had > 300 ng of antibody N/ml. Opsonic activity, after initial and booster vaccinations, correlated with Pn6B-antibody titers. Three infants with nasopharyngeal cultures repeatedly positive for serogroup 6 had poor serum IgG responses. CONCLUSION: Our results demonstrate that Pn6B-TT is safe, elicits functional antibodies and memory responses in infants. |