Safety and immunogenicity of the 23-valent pneumococcal polysaccharide vaccine at 12 months of age, following one, two, or three doses of the 7-valent pneumococcal conjugate vaccine in infancy.
Russell, F; Licciardi, P; Balloch, A; Biaukula, V; Tikoduadua, L; Carapetis, J; Nelson, J; Jenney, A; Waqatakirewa, L; Colquhoun, S; +3 more...Cheung, Y; Tang, M; Mulholland, E
and
(2010)
Safety and immunogenicity of the 23-valent pneumococcal polysaccharide vaccine at 12 months of age, following one, two, or three doses of the 7-valent pneumococcal conjugate vaccine in infancy.
Vaccine, 28 (18).
pp. 3086-3094.
ISSN 0264-410X
DOI: 10.1016/j.vaccine.2010.02.065
Fijian infants aged 6 weeks were stratified by ethnicity and randomized to receive 0, 1, 2, or 3 PCV-7 doses with or without the 23-valent pneumococcal polysaccharide vaccine (PPV-23) at 12 months. Strong booster effects for all 7 PCV-7 serotypes were elicited, and for 4/7 serotypes these responses were highest in the single PCV-7 group. There were fourfold rises in GMC for all non-PCV-7 serotypes. By 17 months the PPV-23 group still had significantly higher GMC (each p<0.001) for all serotypes. The PPV-23 was well tolerated and induced excellent responses for all serotypes which were greatest in the single PCV-7 group.
Item Type | Article |
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ISI | 277064500004 |
Date Deposited | 27 Jul 2013 05:56 |
Explore Further
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857918 (OA Location)
- 10.1016/j.vaccine.2010.02.065 (DOI)
- 20199764 (PubMed)
ORCID: https://orcid.org/0000-0001-7947-680X