Division of Preparedness and Emerging InfectionsNational Center for Emerging and Zoonotic Infectious DiseasesArctic Investigations ProgramCenters for Disease Control and PreventionAnchorageAlaskaUSA.
Epidemiology and Surveillance BranchDivision of Viral HepatitisNational Center for HIV/AIDSViral HepatitisSexually Transmitted Disease, and Tuberculosis PreventionCenters for Disease Control and PreventionAtlantaGeorgiaUSA.
Hepatology. 2022 Oct;76(4):1180-1189. doi: 10.1002/hep.32474. Epub 2022 May 19.
The duration of protection from hepatitis B vaccination in children and adults is not known. In 1981, we used three doses of plasma-derived hepatitis B vaccine to immunize a cohort of 1578 Alaska Native adults and children from 15 Alaska communities who were ≥6 months old.
We tested persons for antibody to hepatitis B surface antigen (anti-HBs) levels 35 years after receiving the primary series. Those with levels <10 mIU/ml received one booster dose of recombinant hepatitis B vaccine 2-4 weeks later and were then evaluated on the basis of anti-HBs measurements 30 days postbooster. Among the 320 recruited, 112 persons had not participated in the 22- or 30-year follow-up study (group 1), and 208 persons had participated but were not given an HBV booster dose (group 2). Among the 112 persons in group 1 who responded to the original primary series, 53 (47.3%) had an anti-HBs level ≥10 mIU/ml. Among group 1, 73.7% (28 of 38) of persons available for a booster dose responded to it with an anti-HBs level ≥10 mIU/ml at 30 days. Initial anti-HBs level after the primary series was correlated with higher anti-HBs levels at 35 years. Among 8 persons who tested positive for antibody to hepatitis B core antigen, none tested positive for HBsAg or HBV DNA.
Based on anti-HBs level ≥10 mIU/ml at 35 years and a 73.7% booster dose response, we estimate that 86% of participants had evidence of protection 35 years later. Booster doses are not needed in the general population at this time.
目前尚不清楚乙型肝炎疫苗对儿童和成人的保护作用能持续多久。1981 年,我们使用三剂血浆衍生乙型肝炎疫苗对来自阿拉斯加 15 个社区的 1578 名≥6 月龄的阿拉斯加原住民成人和儿童进行了免疫接种。
在接受基础系列免疫接种 35 年后,我们对这些人进行了乙型肝炎表面抗原抗体(抗-HBs)检测。抗-HBs 水平<10 mIU/ml 的人在 2-4 周后接受了 1 剂重组乙型肝炎疫苗加强针,之后根据加强针后 30 天的抗-HBs 检测结果进行评估。在招募的 320 人中,有 112 人未参加 22 年或 30 年随访研究(第 1 组),208 人参加了但未接种乙型肝炎病毒加强针(第 2 组)。在第 1 组中,112 名对原始基础系列有反应的人中,53 人(47.3%)的抗-HBs 水平≥10 mIU/ml。在第 1 组中,73.7%(28/38)有加强针接种条件的人在加强针接种后 30 天的抗-HBs 水平≥10 mIU/ml。基础系列免疫接种后初始抗-HBs 水平与 35 年后的高抗-HBs 水平相关。在 8 名乙型肝炎核心抗原抗体检测阳性的人中,均未检测到乙型肝炎表面抗原或乙型肝炎病毒 DNA 阳性。
根据 35 年时抗-HBs 水平≥10 mIU/ml 和 73.7%的加强针接种反应率,我们估计 86%的参与者在 35 年后仍有保护作用。目前不需要在普通人群中接种加强针。