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

To evaluate the immunogenicity and tolerability of Epaxal ® 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 ® and a booster dose after 12 months. Anti-HA...

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Bibliographic Details
Published in:Vaccine 2003-11, Vol.21 (31), p.4588-4592
Main Authors: Usonis, V., Bakasénas, V., Valentelis, R., Katiliene, G., Vidzeniene, D., Herzog, C.
Format: Article
Language:English
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Summary:To evaluate the immunogenicity and tolerability of Epaxal ® 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 ® 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 ≥20 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 ® were well tolerated. These preliminary data suggest that Epaxal ® is an effective hepatitis A vaccine for children and infants from 6 months of age.
ISSN:0264-410X
1873-2518
DOI:10.1016/S0264-410X(03)00509-7