Immunogenicity of the 10-valent pneumococcal non-typeable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) when coadministered with different neisseria meningitidis serogroup C conjugate vaccines.

Jacek Wysocki, Juan C Tejedor, Dutlef Grunert, Ryszard Konior, Jose Garcia-Sicilia, Markus Knuf, Laurence Bernard, Ilse Dieussaert, Lode Schuerman
Author Information
  1. Jacek Wysocki: University School of Medical Sciences & Regional Medical Center for Mother and Child, Poznan, Poland.

Abstract

BACKGROUND: Immunogenicity of the candidate 10-valent pneumococcal non-typeable Haemophilus influenzae protein D-conjugate vaccine (PHiD-CV) was assessed when coadministered with other routine pediatric vaccines including different Neisseria meningitidis serogroup C conjugate vaccines.
METHODS: One thousand five hundred forty-eight healthy infants received, according to a balanced (1:1:1:1) randomization, either PHiD-CV coadministered with (1) DTPa-HBV-IPV/Hib (Infanrix hexa) and MenC-CRM (Meningitec), (2) DTPa-HBV-IPV/Hib and MenC-TT (NeisVac-C), or (3) DTPa-HBV-IPV (Infanrix penta/Pediarix) and Hib-MenC-TT (Menitorix); or 7vCRM (Prevenar/Prevnar) coadministered with DTPa-HBV-IPV and Hib-MenC-TT at 2-4-6 months of age with a booster dose at 11-18 months. Serotype-specific pneumococcal responses were measured by 22F-inhibition ELISA and opsonophagocytic (OPA) assay.
RESULTS: In all 3 coadministration groups, PHiD-CV was immunogenic for each of the 10 pneumococcal vaccine serotypes as assessed by post-primary and post-booster antibody ELISA and OPA responses. When coadministered with DTPa-HBV-IPV, Hib, and MenC antigens, PHiD-CV responses after the third primary dose were within the same range as 7vCRM responses in terms of the percentage of subjects achieving an ELISA antibody concentration >or=0.2 microg/mL for all common vaccine serotypes (over 92% of subjects) except for serotype 6B (at least 87% of subjects). ELISA and OPA immune responses were also evident after the second primary doses of PHiD-CV or 7vCRM vaccine, although antibody levels were below that achieved after 3 primary doses, particularly for serotypes 6B and 23F. The kinetics of the immune responses from after the second dose to after the booster dose were similar for most of the serotypes in both PHiD-CV and 7vCRM groups.
CONCLUSIONS: PHiD-CV was immunogenic when coadministered with other routine pediatric vaccines including MenC conjugate vaccines.

Associated Data

ClinicalTrials.gov | NCT00334334; NCT00463437

MeSH Term

Antibodies, Bacterial
Bacterial Proteins
Carrier Proteins
Diphtheria-Tetanus-Pertussis Vaccine
Diphtheria-Tetanus-acellular Pertussis Vaccines
Enzyme-Linked Immunosorbent Assay
Female
Hepatitis B Vaccines
Humans
Immunization, Secondary
Immunoglobulin D
Infant
Lipoproteins
Male
Meningococcal Infections
Meningococcal Vaccines
Neisseria meningitidis, Serogroup C
Opsonin Proteins
Phagocytosis
Pneumococcal Infections
Pneumococcal Vaccines
Poliovirus Vaccine, Inactivated
Serotyping
Streptococcus pneumoniae
Treatment Outcome
Vaccination
Vaccines, Combined
Vaccines, Conjugate

Chemicals

Antibodies, Bacterial
Bacterial Proteins
Carrier Proteins
Diphtheria-Tetanus-Pertussis Vaccine
Diphtheria-Tetanus-acellular Pertussis Vaccines
Hepatitis B Vaccines
Immunoglobulin D
Lipoproteins
Meningococcal Vaccines
Opsonin Proteins
PEDIARIX
Pneumococcal Vaccines
Poliovirus Vaccine, Inactivated
Vaccines, Combined
Vaccines, Conjugate
glpQ protein, Haemophilus influenzae

Word Cloud

Created with Highcharts 10.0.0PHiD-CVcoadministeredresponsesvaccinevaccinespneumococcalconjugate7vCRMdoseELISAserotypes3DTPa-HBV-IPVOPAantibodyprimarysubjectsImmunogenicity10-valentnon-typeableHaemophilusinfluenzaeproteinassessedroutinepediatricincludingdifferentmeningitidisserogroupCDTPa-HBV-IPV/HibInfanrix2Hib-MenC-TTmonthsboostergroupsimmunogenicMenC6BimmuneseconddosesBACKGROUND:candidateD-conjugateNeisseriaMETHODS:Onethousandfivehundredforty-eighthealthyinfantsreceivedaccordingbalanced1:1:1:1randomizationeither1hexaMenC-CRMMeningitecMenC-TTNeisVac-Cpenta/PediarixMenitorixPrevenar/Prevnar2-4-6age11-18Serotype-specificmeasured22F-inhibitionopsonophagocyticassayRESULTS:coadministration10post-primarypost-boosterHibantigensthirdwithinrangetermspercentageachievingconcentration>or=0microg/mLcommon92%exceptserotypeleast87%alsoevidentalthoughlevelsachievedparticularly23FkineticssimilarCONCLUSIONS:Dneisseria

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