Administration of hepatitis A vaccine at 6 and 12 months of age concomitantly with hexavalent (DTaP-IPV-PRP∼T-HBs) combination vaccine

被引:10
|
作者
Stojanov, S.
Liese, J. G.
Belohradsky, B. H.
Vandermeulen, C.
Hoppenbrouwers, K.
Van der Wielen, M.
Van Damme, P.
Georges, B.
Dupuy, M.
Scemama, M.
Watson, M.
Fiquet, A.
Stek, J. E.
Golm, G. T.
Schoedel, F. P.
Kuter, B. J.
机构
[1] Univ Munich, Univ Childrens Hosp, Munich, Germany
[2] Katholieke Univ Leuven, Dept Youth Hlth Care, Louvain, Belgium
[3] Univ Antwerp, Ctr Evaluat Vaccinat, B-2020 Antwerp, Belgium
[4] Sanofi Pasteur SA, Lyon, France
[5] Sanofi Pasteur MSD, Lyon, France
[6] Merck Res Labs, West Point, PA USA
关键词
hepatitis A; VAQTA (R); hexavalent; HEXAVAC (R); concomitant use; immunization; infant; vaccines;
D O I
10.1016/j.vaccine.2007.08.028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Administration of two doses of hepatitis A (HA) vaccine to children > 2 years of age has been shown to be protective. The present study assessed whether HA vaccine can be administered as early as 6 months of age and whether it can be administered concomitantly with a hexavalent (HV) vaccine at this age. Methods: In an open label, randomized, parallel group study, the liquid HV vaccine (HEXAVACO) (diphtheria, tetanus, 2-component acellular pertussis, inactivated poliomyelitis vaccine, Haemophilus influenzae type b conjugated to tetanus protein and hepatitis 13) was administered at 2, 4, 6, and 12 months of age to all children. HA vaccine (VAQTA) was given at 7 and 13 months in the separate administration group (Group 1) and at 6 and 12 months in the concomitant administration group (Group 2). Serum samples were obtained at 2, 7, 12, and 14 months in Group 1 and at 2, 7, 12, and 13 months in Group 2. The primary immunogenicity outcomes were the seroconversion rates for HA 1 month after the second dose of HA vaccine in initially seronegative subjects, and the seroconversion rates for each HV antigen 1 month after the third dose of the HV vaccine (both at 7 months of age). Results: HA seropositivity rates 1 month after the second dose were 100% in both groups, regardless of initial serostatus. The responses to each HV antigen 1 month after the third dose were similar in both groups. The vaccines were generally well tolerated in both groups regardless of vaccine(s) administered. Conclusions: A schedule of two doses of HA vaccine, 6 months apart beginning at 6 months of age is highly immunogenic and well tolerated when administered alone or concomitantly with HV vaccine at 6 and 12 months of age. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7549 / 7558
页数:10
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