Long-Term Efficacy of a Hepatitis E Vaccine

被引:254
作者
Zhang, Jun [1 ]
Zhang, Xue-Feng [3 ]
Huang, Shou-Jie [1 ]
Wu, Ting [1 ]
Hu, Yue-Mei [3 ]
Wang, Zhong-Ze [4 ]
Wang, Hua [3 ]
Jiang, Han-Min [4 ]
Wang, Yi-Jun [4 ]
Yan, Qiang [2 ]
Guo, Meng [2 ]
Liu, Xiao-Hui [2 ]
Li, Jing-Xin [3 ]
Yang, Chang-Lin [4 ]
Tang, Quan [5 ]
Jiang, Ren-Jie [5 ]
Pan, Hui-Rong [2 ]
Li, Yi-Min [2 ]
Shih, J. Wai-Kuo [1 ]
Ng, Mun-Hon [1 ]
Zhu, Feng-Cai [3 ]
Xia, Ning-Shao [1 ]
机构
[1] Xiamen Univ, Natl Inst Diagnost & Vaccine Dev Infect Dis, State Key Lab Mol Vaccinol & Mol Diagnost, Collaborat Innovat Ctr Biol Prod,Sch Publ Hlth, Xiamen 361102, Peoples R China
[2] Xiamen Innovax Biotech Co, Xiamen, Peoples R China
[3] Jiangsu Prov Ctr Dis Control & Prevent, Nanjing 210009, Jiangsu, Peoples R China
[4] Dongtai Ctr Dis Control & Prevent, Dongtai, Peoples R China
[5] Yancheng Ctr Dis Control & Prevent, Yancheng, Peoples R China
关键词
E VIRUS-INFECTION; DEVELOPED-COUNTRIES; VIRAL-HEPATITIS; PREGNANCY;
D O I
10.1056/NEJMoa1406011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Hepatitis E virus (HEV) is a leading cause of acute hepatitis. The long-term efficacy of a hepatitis E vaccine needs to be determined. METHODS In an initial efficacy study, we randomly assigned healthy adults 16 to 65 years of age to receive three doses of either a hepatitis E vaccine (vaccine group; 56,302 participants) or a hepatitis B vaccine (control group; 56,302 participants). The vaccines were administered at 0, 1, and 6 months, and the participants were followed for 19 months. In this extended follow-up study, the treatment assignments of all participants remained double-blinded, and follow-up assessments of efficacy, immunogenicity, and safety were continued for up to 4.5 years. RESULTS During the 4.5-year study period, 60 cases of hepatitis E were identified; 7 cases were confirmed in the vaccine group (0.3 cases per 10,000 person-years), and 53 cases in the control group (2.1 cases per 10,000 person-years), representing a vaccine efficacy of 86.8% (95% confidence interval, 71 to 94) in the modified intention-to-treat analysis. Of the participants who were assessed for immunogenicity and were seronegative at baseline, 87% of those who received three doses of the hepatitis E vaccine maintained antibodies against HEV for at least 4.5 years; HEV antibody titers developed in 9% in the control group. The rate of adverse events was similar in the two groups. CONCLUSIONS Immunization with this hepatitis E vaccine induced antibodies against HEV and provided protection against hepatitis E for up to 4.5 years. (Funded by the Chinese Ministry of Science and Technology and others; ClinicalTrials.gov number, NCT01014845.)
引用
收藏
页码:914 / 922
页数:9
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