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J Infect Dis ; 180(6): 2018-22, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10558961

RESUMO

A randomized trial comparing 3 manufacturing consistency lots of a combination hepatitis A/hepatitis B vaccine to each other and to hepatitis A vaccine and hepatitis B vaccine given separately and concurrently was done to evaluate safety, tolerability, and immunogenicity. Healthy volunteers >/=11 years of age were divided into 4 groups. Each of 3 groups received a separate consistency lot of the combination vaccine, and 1 group received separate but concurrent injections of hepatitis A and hepatitis B vaccines. Injections were given at weeks 0 and 24. The combination vaccine was generally well tolerated. The hepatitis A portion of the combination vaccine produced clinically acceptable high seropositivity rates 4 and 52 weeks after the first injection. The hepatitis B portion of the vaccine did not produce clinically acceptable seropositivity rates 4 weeks after the second injection. Lack of antibody production may be attributed, at least in part, to immunologic interference.


Assuntos
Anticorpos Anti-Hepatite B/biossíntese , Antígenos de Superfície da Hepatite B/imunologia , Vacinas contra Hepatite B/imunologia , Vacinas Combinadas/imunologia , Vacinas contra Hepatite Viral/imunologia , Adolescente , Adulto , Criança , Feminino , Vacinas contra Hepatite A , Vacinas contra Hepatite B/administração & dosagem , Vírus da Hepatite B/imunologia , Hepatovirus/imunologia , Humanos , Masculino , Vacinação , Vacinas Combinadas/administração & dosagem , Vacinas contra Hepatite Viral/administração & dosagem
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