Antibody titres after primary and booster vaccination of infants and young children with a virosomal hepatitis A vaccine (Epaxal®)

被引:50
|
作者
Usonis, V
Bakasénas, V
Valentelis, R
Katiliene, G
Vidzeniene, D
Herzog, C
机构
[1] Vilnius State Univ, Ctr Paediat, LT-2009 Vilnius, Lithuania
[2] Berna Biotech Ltd, CH-3018 Bern, Switzerland
[3] Pylimo Out Patient Clin, LT-2100 Vilnius, Lithuania
[4] Republican Immunisat Ctr, LT-2040 Vilnius, Lithuania
关键词
hepatitis A; vaccine; epaxal((R)); aluminium-free vaccine; virosomes;
D O I
10.1016/S0264-410X(03)00509-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To evaluate the immunogenicity and tolerability of Epaxal(R) in infants and children, 30 infants (aged 6-7 months) and 30 children (aged 5-7 years) received a single intramuscular dose of the aluminium-free virosomal hepatitis A virus (HAV) vaccine Epaxal(R) and a booster dose after 12 months. Anti-HAV antibody titres were measured at baseline (before injection), at 1 and 12 months after primary vaccination, and 1 month after the booster vaccination. Sixteen evaluable infants had maternal anti-HAV antibodies at baseline. Complete seroprotection (titre greater than or equal to20 mIU/ml) was achieved by all infants and children at Month 1 and at Month 12. Additionally, all subjects showed a strong antibody response to booster vaccination. In infants without maternal anti-HAV antibodies, the response was four-fold higher than in those with maternal anti-HAV antibodies. Both doses of Epaxal(R) were well tolerated. These preliminary data suggest that Epaxal(R) is an effective hepatitis A vaccine for children and infants from 6 months of age. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4588 / 4592
页数:5
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