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DOI 10.1097/inf.0b013e31828d6b20

Медицинская библиотека · The Pediatric infectious disease journal · 2013

A randomized, controlled trial to assess the immunogenicity and safety of a heptavalent diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis, hib and meningococcal serogroup C combination vaccine administered at 2, 3, 4 and 12-18 months of age.

Szenborn Leszek, Czajka Hanna, Brzostek Jerzy, Konior Ryszard, Caubet Magalie, Ulianov Liliana, Leyssen Maarten

Клиническое исследование II фазыСтатьяРандомизированное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Combination vaccines offer protection against multiple diseases with fewer injections. This study evaluated the immunogenicity and safety of an investigational diphtheria, tetanus, acellular pertussis, hepatitis B, poliomyelitis, Haemophilus influenzae type b (Hib) and meningococcal serogroup C (MenC) heptavalent combination vaccine (heptavalent vaccine) given as 4 doses at 2, 3, 4 and 12-18 months of age.

METHODS

In this randomized, open, phase II study (NCT00970307/NCT01171989) conducted in Poland, 421 infants were enrolled to receive the heptavalent vaccine or licensed comparator vaccines. Immunogenicity against study vaccine antigens was measured prior to and 1 month after primary and booster vaccinations. Safety and reactogenicity of the vaccines were also evaluated.

RESULTS

The primary noninferiority objectives of the MenC and Hib immune responses induced by the heptavalent vaccine versus comparator vaccines were reached after primary vaccination, but no statistical conclusion could be drawn after booster dose. One month after primary and booster vaccinations, ≥98.4% of the heptavalent vaccine recipients were seroprotected for MenC and Hib. Exploratory analyses indicated that the heptavalent vaccine induced higher postprimary vaccination antibody geometric mean concentrations against Hib, but lower postprimary and postbooster vaccinations geometric mean titers against MenC compared with the relevant comparator vaccines. The reactogenicity profiles of the vaccines were acceptable, although 1 infant vaccinated with the heptavalent vaccine experienced a serious adverse event (thrombocytopenia) considered possibly related to vaccination.

CONCLUSIONS

The heptavalent vaccine was immunogenic and had a clinically acceptable safety profile when administered to infants and toddlers.

Для цитирования: Szenborn Leszek, Czajka Hanna, Brzostek Jerzy, Konior Ryszard, Caubet Magalie, Ulianov Liliana, Leyssen Maarten. A randomized, controlled trial to assess the immunogenicity and safety of a heptavalent diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis, hib and meningococcal serogroup C combination vaccine administered at 2, 3, 4 and 12-18 months of age.. The Pediatric infectious disease journal. 2013. DOI: 10.1097/inf.0b013e31828d6b20.

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