Pneumococcal Protein-D Conjugate Vaccine Safe to Coadminister With Other Routine Vaccinations: Presented at ESPID
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Pneumococcal Protein-D Conjugate Vaccine Safe to Coadminister With Other Routine Vaccinations: Presented at ESPID

By Jenny Powers

NICE, France -- May 12, 2010 -- Antibody responses elicited by pneumococcal nontypeable Haemophilus influenzae protein-D conjugate vaccine (PHiD-CV) coadministered with the diphtheria, tetanus, pertussis (DTaP), hepatitis B virus (HBV), poliomyelitis (IPV), and H influenzae type b (Hib) vaccine (DTaP-HBV-IPV-HiB) or DTaP-IPV-HiB were comparable for all vaccine pneumococcal serotypes except 18C, researchers reported here at the 28th Annual Meeting of the European Society for Paediatric Infectious Diseases (ESPID).

Menno R. van den Bergh, MD, Department of Paediatric Immunology and Infectious Disease, University Medical Center, Utrecht, and the Department of Paediatrics of the Spaarne Hospital, Hoofddorp, Netherlands, presented the results here on May 7.
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The primary objective of his single-centre, single-blind study was to demonstrate noninferiority of PHiD-CV when coadministered with DTaP-IPV-Hib (group 2) as compared with the DTaP-HBV-IPV-HiB vaccine (group 1) at 1 month after the third dose in 520 healthy infants.

Vaccines were given when the infants were aged 2, 3, and 4 months.

Noninferiority of group 2 versus group 1 was demonstrated for protein D against all vaccine pneumococcal serotypes except 18C.

For each vaccine pneumococcal serotype including 18C, percentages of infants reaching enzyme-linked immunosorbent assay (ELISA) 0.2 mcg/mL were in the same ranges for both PHiD-CV groups.

For each vaccine group pneumococcal serotype including 18C, the percentages of infants reaching 33F-ELISA 0.2 mcg/mL and percentages reaching an opsonophagocytic activity titre of 8 were in the same ranges for both treatment groups.

The lower antibody geometric mean concentrations for serotype 18C could be related to observed differences in anti-tetanus response, which were higher in group 1.

Funding for this study was provided by GlaxoSmithKline.

[Presentation title: Immunogenicity of PHiD-CV 3-Dose Primary Vaccination Co-Administered With Pediacel or Infanrix Hexa in the Netherlands. Abstract 24]

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