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Anamnestic Immune Response in 3- to 4-year-old Children Previously Immunized With 10-valent Pneumococcal Nontypeable Haemophilus influenzae Protein D Conjugate Vaccine as 2-dose or 3-dose Priming and a Booster Dose in the First Year of Life
- Source :
- Pediatric Infectious Disease Journal. 30:e155-e163
- Publication Year :
- 2011
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2011.
-
Abstract
- Immunogenicity of 10-valent pneumococcal nontypeable Haemophilus influenzae protein d conjugate vaccine (PHiD-CV), administered as 2-dose or 3-dose priming followed by a booster dose, has been described previously. The present study evaluated immunologic memory following PHiD-CV vaccination according to these vaccination schedules.A dose of PHiD-CV (to test anamnestic responses) was administered to 172 children at 36 to 46 months of age; 110 of them had previously been vaccinated with PHiD-CV according to 2 + 1 or 3 + 1 schedules (PHiD-CV [2 + 1] and PHiD-CV [3 + 1] groups) and 62 were unprimed age-matched controls. To measure immune responses before and 7 to 10 days after the PHiD-CV dose, 22F-inhibition enzyme-linked immunosorbent assay and opsonophagocytic activity (OPA) assay were used.Serotype-specific IgG geometric mean concentrations (GMCs) and OPA geometric mean titers increased substantially (from before to 7 to 10 days after the additional PHiD-CV dose) for all 10 vaccines and 2 cross-reactive serotypes (6A and 19A) in the children previously vaccinated with PHiD-CV, regardless of the vaccination schedule used. Antibody GMCs and OPA geometric mean titers after the administration of the PHiD-CV dose were markedly higher in both previously PHiD-CV-vaccinated groups than in the unprimed control group, clearly demonstrating prior induction of immunologic memory. Antiprotein D antibody GMCs had also increased substantially from before to 7 to 10 days after vaccination in all 3 groups, with higher antibody GMCs in the previously vaccinated groups than in the control group.PHiD-CV vaccination according to 2 + 1 or 3 + 1 schedules resulted in comparable anamnestic immune responses. These findings suggest that similar protective efficacy may be achieved with both the schedules.
- Subjects :
- Male
Microbiology (medical)
Time Factors
Lipoproteins
Priming (immunology)
Booster dose
medicine.disease_cause
complex mixtures
Pneumococcal Infections
Haemophilus influenzae
Pneumococcal Vaccines
Immune system
Bacterial Proteins
Conjugate vaccine
medicine
Humans
Vaccines, Conjugate
biology
business.industry
Immunogenicity
Vaccination
Immunoglobulin D
Antibodies, Bacterial
Virology
Infectious Diseases
Child, Preschool
Immunoglobulin G
Pediatrics, Perinatology and Child Health
Immunology
biology.protein
Female
Antibody
Carrier Proteins
business
Immunologic Memory
Follow-Up Studies
Subjects
Details
- ISSN :
- 08913668
- Volume :
- 30
- Database :
- OpenAIRE
- Journal :
- Pediatric Infectious Disease Journal
- Accession number :
- edsair.doi.dedup.....691074fbdf65b5ad1eeae0f6a09395bc
- Full Text :
- https://doi.org/10.1097/inf.0b013e31821feeb7