Immunogenicity, reactogenicity, and safety of a seven-valent pneumococcal conjugate vaccine (PCV7) concurrently administered with a fully liquid DTPa-IPV-HBV-Hib combination vaccine in healthy infants

被引:32
|
作者
Olivier, C. [1 ]
Belohradsky, B. H. [2 ]
Stojanov, S. [2 ]
Bonnet, E. [3 ]
Petersen, G. [4 ]
Liese, J. G. [2 ]
机构
[1] Hop Louis Mourier, F-92701 Colombes, France
[2] Univ Munich, Dr Von Haunerschen Kinderspital, D-80337 Munich, Germany
[3] Wyeth, Paris, France
[4] Wyeth, Munster, Germany
关键词
seven-valent pneumococcal conjugate vaccine; hexavalent diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated polio virus-Haemophilus influenzae type b vaccine; concomitant administration;
D O I
10.1016/j.vaccine.2007.11.096
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim of the study: To evaluate the immunogenicity, safety and reactogenicity of a seven-vatent pneumococcal conjugate vaccine (PCV7) when given concomitantly with a fully liquid DTaP-IPV-HBV-Hib combination vaccine. Methods: Two hundred and sixty-six healthy infants in France (n = 136) and Germany (n = 130) were randomized to receive DTaP-IPV-HBV-Hib and PCV7 (test group) at the age of 2, 3 and 4 months (primary series) and 12-15 months (booster dose), or to receive DTaP-IPV-HBV-Hib at the same time points but PCV7 at the ages of 5, 6, 7 and 13-16 months (control group). Antibody levels to all. vaccine antigens were measured before dose 1, 1 month after dose 3, at the time of booster, and I month later. Safety data were collected after each vaccine dose. Results: Two hundred and fifty-seven infants (test group, 131; control group, 126) completed the primary immunization series and two hundred and forty-five received the booster dose (test group, 125; control. group, 120). Depending on the serotype, 92.8-100% of subjects in the test group achieved antibody tevels >= 0.15 mu g/mL for PCV7 antigens at 5 months of age, and 89.7-99.1% of them antibody levels >= 0.50 mu g/ml 1 month after booster. For DTaP-IPV-HBV-Hib, there was no statistically significant difference between the two groups in the proportion of infants that achieved pre-defined seroprotective Levels for each antigen at 5 months and 1 month after booster. Frequency of local and systemic reactions was similar in both groups except for fever above 38.0 degrees C, which was more frequent in the test group after dose 1, 2 or 4. Fever >39.0 degrees C was only reported from three children in each group. Conclusion: The PCV7 vaccine was highly immunogenic, well tolerated, and safe when coadministered with the DTPa-IPV-HBV-Hib vaccine at 2, 3, and 4 months of age and a booster dose at 12-15 months. In this study, PCV7 did not show any relevant influence on the immunogenicity and safety of the concurrently administered DTPa-IPV-HBV-Hib vaccine. (C) 2008 Published by Elsevier Ltd.
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收藏
页码:3142 / 3152
页数:11
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