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11-15 岁青少年接种两到三剂乙肝疫苗后的五年随访:一项随机对照研究。

Five years follow-up following two or three doses of a hepatitis B vaccine in adolescents aged 11-15 years: a randomised controlled study.

机构信息

Faculty of Medicine, Vaccine & Infectious Disease Institute (WHO Collaborating Centre), Centre for Evaluation of Vaccination, Antwerpen, Belgium.

出版信息

BMC Infect Dis. 2010 Dec 20;10:357. doi: 10.1186/1471-2334-10-357.

DOI:10.1186/1471-2334-10-357
PMID:21171982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3016379/
Abstract

BACKGROUND

The standard three-dose schedule of hepatitis B vaccines is frequently not completed, especially in adolescents. A primary study has confirmed the equivalence of a two-dose schedule of an Adult formulation of hepatitis B vaccine [Group HBV_2D] to a three-dose schedule of a Paediatric formulation in adolescents (11-15 years) [Group HBV_3D]. This follow-up study evaluated the five year persistence of antibody response and immune memory against the hepatitis B surface (anti-HBs) antigens five years after completion of primary vaccination.

METHODS

A total of 234 subjects returned at the Year 5 time point, of which 144 subjects received a challenge dose of hepatitis B vaccine. Blood samples were collected yearly and pre- and post-challenge dose to assess anti-HBs antibody concentrations.

RESULTS

At the end of five years, 79.5% (95% confidence interval [CI]: 71.7 - 86.1) and 91.4% (95% CI: 82.3 - 96.8) of subjects who received the two-dose and three-dose schedules, respectively had anti-HBs antibody concentrations ≥ 10 mIU/mL. Post-challenge dose, all subjects had anti-HBs antibody concentration ≥ 10 mIU/mL and >94% subjects had anti-HBs antibody concentration ≥ 100 mIU/mL. All subjects mounted a rapid anamnestic response to the challenge dose. Overall, the challenge dose was well-tolerated.

CONCLUSION

The two-dose schedule of hepatitis B vaccine confers long-term immunogenicity and shows evidence of immune memory for at least five years following vaccination.

TRIAL REGISTRATION

Clinical Trials NCT00343915, NCT00524576.

摘要

背景

乙肝疫苗的标准三剂接种方案经常无法完成,尤其是在青少年中。一项初步研究已经证实,成人型乙肝疫苗[HBV_2D 组]两剂方案与青少年(11-15 岁)[HBV_3D 组]三剂方案的等效性。本随访研究评估了原发性免疫接种完成五年后,乙型肝炎表面(抗-HBs)抗原的抗体反应和免疫记忆的五年持续情况。

方法

共有 234 名受试者在第 5 年时间点返回,其中 144 名受试者接受了乙肝疫苗挑战剂量。每年采集血样,在接种前和接种后评估抗-HBs 抗体浓度。

结果

五年结束时,分别接受两剂和三剂方案的受试者中,有 79.5%(95%置信区间[CI]:71.7-86.1)和 91.4%(95% CI:82.3-96.8)的受试者抗-HBs 抗体浓度≥10 mIU/mL。接种挑战剂量后,所有受试者的抗-HBs 抗体浓度均≥10 mIU/mL,超过 94%的受试者的抗-HBs 抗体浓度≥100 mIU/mL。所有受试者对挑战剂量均产生了快速的记忆反应。总体而言,该挑战剂量具有良好的耐受性。

结论

乙肝疫苗两剂方案可提供长期的免疫原性,并在接种后至少五年内显示出免疫记忆的证据。

试验注册

临床试验 NCT00343915、NCT00524576。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/e88c3cc652fe/1471-2334-10-357-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/9d4105359a4a/1471-2334-10-357-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/481d1eafde10/1471-2334-10-357-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/e88c3cc652fe/1471-2334-10-357-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/9d4105359a4a/1471-2334-10-357-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/481d1eafde10/1471-2334-10-357-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/3016379/e88c3cc652fe/1471-2334-10-357-3.jpg

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