Three-Year Antibody Persistence and Safety following a Single Dose of Combined Haemophilus influenzae Type b-Neisseria meningitidis Serogroup C-Tetanus Toxoid Conjugate Vaccine in Hib-Primed Toddlers

dc.contributor.authorBooy, Robert
dc.contributor.authorRichmond, Peter
dc.contributor.authorNolan, Terry
dc.contributor.authorMcVernon, Jodie
dc.contributor.authorMarshall, Helen
dc.contributor.authorNissen, Michael
dc.contributor.authorReynolds, Graham
dc.contributor.authorZiegler, John B
dc.contributor.authorStoney, Tanya
dc.contributor.authorHeron, L
dc.contributor.authorLambert, Stephen
dc.contributor.authorMesaros, Narcisa
dc.contributor.authorPeddiraju, Kavitha
dc.contributor.authorMiller, Jacqueline M
dc.date.accessioned2015-12-10T22:20:48Z
dc.date.available2015-12-10T22:20:48Z
dc.date.issued2013
dc.date.updated2016-02-24T11:31:42Z
dc.description.abstractBACKGROUND: Persistence of seroprotective bactericidal antibody titers is important for long-term protection against meningococcal serogroup C disease in young children. Antibody persistence values were determined in children up to 3 years after vaccination with a single dose of the combined Haemophilus influenzae type b (Hib)-Neisseria meningitidis serogroup C (MenC)-tetanus toxoid (TT) conjugate vaccine (Hib-MenC-TT; www.ClinicalTrials.gov: NCT00326118). METHODS: The children had been randomized at ages 12-18 months to receive either 1 dose of Hib-MenC-TT (Hib-MenC group) or separately administered Hib-TT conjugate vaccine and MenC-CRM197 (MCC) vaccine (Hib plus MCC group). All children had been primed in infancy with a Hib vaccine. Antibodies against MenC were measured by a serum bactericidal assay using rabbit complement (rSBA-MenC) and antibodies against Hib polyribosylribitol phosphate were assessed by enzyme-linked immunosorbent assay. RESULTS: The rSBA-MenC titers ≥1:8 were demonstrated 3 years after vaccination in 64.2% and 53.2% of participants in the Hib-MenC group and in the Hib plus MCC group, respectively. Antipolyribosylribitol phosphate concentrations ≥0.15 μg/mL persisted in >98% of participants in both groups. The rSBA-MenC geometric mean titers and antipolyribosylribitol phosphate geometric mean concentrations remained higher 3 years after vaccination than before vaccination. No serious adverse events assessed by the investigator as being related to vaccination were reported. CONCLUSION: In this antibody persistence study of Hib-primed but MenC-naïve toddlers who received a single dose of Hib-MenC-TT, protective antibody levels against Hib and MenC were maintained in the majority of children 3 years after vaccination.
dc.identifier.issn0891-3668
dc.identifier.urihttp://hdl.handle.net/1885/52085
dc.publisherLippincott Williams & Wilkins
dc.sourceThe Pediatric Infectious Disease Journal
dc.subjectKeywords: Haemophilus influenzae type b vaccine; tetanus toxoid; antibody titer; article; child; controlled study; enzyme linked immunosorbent assay; female; Haemophilus influenzae type b; human; infancy; infant; male; multicenter study; Neisseria meningitidis; pre antibody persistence; Haemophilus influenzae type b; Neisseria meningitidis serogroup C; toddlers
dc.titleThree-Year Antibody Persistence and Safety following a Single Dose of Combined Haemophilus influenzae Type b-Neisseria meningitidis Serogroup C-Tetanus Toxoid Conjugate Vaccine in Hib-Primed Toddlers
dc.typeJournal article
local.bibliographicCitation.issue2
local.bibliographicCitation.lastpage174
local.bibliographicCitation.startpage169
local.contributor.affiliationBooy, Robert, Children's Hospital at Westmead
local.contributor.affiliationRichmond, Peter, University of Western Australia
local.contributor.affiliationNolan, Terry, University of Melbourne
local.contributor.affiliationMcVernon, Jodie, University of Melbourne
local.contributor.affiliationMarshall, Helen, University of Adelaide
local.contributor.affiliationNissen, Michael, Royal Children's Hospital
local.contributor.affiliationReynolds, Graham, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationZiegler, John B, Sydney Children's Hospital
local.contributor.affiliationStoney, Tanya, Telethon Institute for Child Health Research
local.contributor.affiliationHeron, L, Children's Hospital at Westmead
local.contributor.affiliationLambert, Stephen, Royal Children's Hospital
local.contributor.affiliationMesaros, Narcisa, GlaxoSmithKline Biologicals
local.contributor.affiliationPeddiraju, Kavitha, GlaxoSmithKline Biologicals
local.contributor.affiliationMiller, Jacqueline M, GlaxoSmithKline Biologicals
local.contributor.authoruidReynolds, Graham, u4043307
local.description.notesImported from ARIES
local.identifier.absfor111403 - Paediatrics
local.identifier.ariespublicationu4971216xPUB238
local.identifier.citationvolume32
local.identifier.doi10.1097/INF.0b013e3182787bff
local.identifier.scopusID2-s2.0-84873056841
local.identifier.thomsonID000313874500021
local.type.statusPublished Version

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