Antibody Persistence and Immune Memory in Healthy Adults Following Vaccination With a Two-Dose Inactivated Hepatitis A Vaccine: Long-Term Follow-Up at 15 Years

被引:31
作者
Van Herck, Koen [2 ]
Jacquet, Jeanne-Marie [3 ]
Van Damme, Pierre [1 ]
机构
[1] Univ Antwerp, Ctr Evaluat Vaccinat, Vaccine & Infect Dis Inst, WHO Collaborating Ctr,Fac Med, B-2610 Antwerp, Belgium
[2] Univ Ghent, Dept Publ Hlth, B-9000 Ghent, Belgium
[3] GlaxoSmithKline Biol, Wavre, Belgium
关键词
persistence; immune response; hepatitis A vaccine; IMMUNOGENICITY; IMMUNIZATION; PROGRAM;
D O I
10.1002/jmv.22200
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Long-term persistence of vaccine-induced immune response in adults was assessed annually for 15 years following primary immunization with a two-dose inactivated hepatitis A vaccine. In 1992, 119 and 194 subjects aged 17 40 years and naive for hepatitis A virus (HAV) were enrolled in two studies to receive 1,440 ELISA units (EI.U) of inactivated hepatitis A vaccine (Havrix (TM), GlaxoSmithKline Biologicals, Belgium) according to a standard 0, 6 or an extended 0, 12 months schedule, respectively. Serum samples were taken 1 month after the second vaccine dose and every consecutive year up to 15 years after primary vaccination for measurement of anti-HAV antibody concentrations (NCT00291876 and NCT00289757). At year 15, 100% (48/48) and 97.3% (108/111) of subjects vaccinated at 0, 6 or 0, 12 months remained seropositive for anti-HAV antibodies, with geometric mean concentrations (GMCs) of 289.2 and 367.4 mIU/ml, respectively. An additional dose of HAV vaccine (1,440 EI.U) was administered to the six subjects who had become seronegative for anti-HAV antibodies since year 11. All subjects mounted a humoral immune response to the additional HAV challenge dose, although post-challenge anti-HAV antibody levels remained low in one subject. These studies represent the longest annual follow-up of hepatitis A vaccine in healthy adults. The immune response induced by two doses of this inactivated HAV vaccine was shown to persist for at least 15 years. No difference in long-term antibody persistence was observed between the two primary vaccination schedules, reinforcing the potential for flexibility in the timing of the second primary vaccine dose. J. Med. Virol. 83:1885-1891, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1885 / 1891
页数:7
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