Hammitt Laura L, Bulkow Lisa, Hennessy Thomas W, Zanis Carolyn, Snowball Mary, Williams James L, Bell Beth P, McMahon Brian J
Arctic Investigations Program, National Center for Preparedness, Detection and Control of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
J Infect Dis. 2008 Dec 15;198(12):1776-82. doi: 10.1086/593335.
Hepatitis A vaccination is effective in preventing disease. However, the duration of protection after vaccination is unknown.
We enrolled persons who responded to a 3-dose primary series of hepatitis A vaccine. For adults, the first dose was 720 ELISA units (EU) of hepatitis A vaccine, readministered at 1 and 12 months after the first vaccination (hereafter, "0-1-12 months"); for children aged 3-6 years, the first dose was 360 EU, readministered according to 1 of 3 vaccination schedules: 1 and 2 months after the first vaccination ("0-1-2 months"), 1 and 6 months after the first vaccination ("0-1-6 months"), or 1 and 12 months after vaccination ("0-1-12 months"). Specimens collected 1 month and 1-10 years after vaccination were tested for antibody to hepatitis A virus (anti-HAV) by ELISA. Long-term antibody persistence was estimated by using the observed rate of decline in geometric mean concentration (GMC).
A total of 144 children and 128 adults were enrolled. Children vaccinated at 0-1-2 months had a significantly lower GMC of antibody than children vaccinated at 0-1-12 months, but this difference was statistically significant only through 4 years of follow-up. All 67 children tested at 10 years and 25 (96%) of 26 adults tested at 8-9 years had detectable anti-HAV. The estimated duration of antibody persistence was 21-27 years, depending on the vaccination schedule.
Anti-HAV persists in adults and children for more than 10 years after the primary vaccination series. Additional studies are needed to evaluate the duration of antibody persistence beyond 10 years and to assess the long-term immunogenicity of the currently recommended 2-dose schedule.
甲型肝炎疫苗在预防疾病方面有效。然而,接种疫苗后的保护持续时间尚不清楚。
我们招募了对3剂甲型肝炎疫苗基础免疫系列有反应的人。对于成年人,第一剂为720酶联免疫吸附测定单位(EU)的甲型肝炎疫苗,在首次接种后1个月和12个月再次接种(以下简称“0-1-12个月”);对于3至6岁的儿童,第一剂为360 EU,根据3种接种程序中的1种再次接种:首次接种后1个月和2个月(“0-1-2个月”)、首次接种后1个月和6个月(“0-1-6个月”)或接种后1个月和12个月(“0-1-12个月”)。在接种疫苗后1个月和1至10年采集的样本通过酶联免疫吸附测定法检测甲型肝炎病毒抗体(抗-HAV)。通过观察几何平均浓度(GMC)的下降率来估计长期抗体持久性。
共招募了144名儿童和128名成年人。在0-1-2个月接种疫苗的儿童的抗体GMC显著低于在0-1-12个月接种疫苗的儿童,但这种差异仅在4年的随访中具有统计学意义。在10岁时检测的所有67名儿童以及在8至9岁时检测的26名成年人中的25名(96%)都有可检测到的抗-HAV。根据接种程序,抗体持久性的估计持续时间为21至27年。
在完成基础免疫接种系列后,抗-HAV在成年人和儿童中持续存在超过10年。需要进一步研究来评估抗体持久性超过10年的持续时间,并评估当前推荐的2剂接种程序的长期免疫原性。