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一项在中国婴幼儿、儿童和青少年中比较两种甲型肝炎灭活疫苗免疫原性和安全性的开放性、前瞻性、随机研究。

An open, prospective, randomized study comparing the immunogenicity and safety of two inactivated hepatitis A pediatric vaccines in toddlers, children and adolescents in China.

机构信息

Guangxi Zhuang Autonomous Region Center for Disease Prevention and Control, Center for Vaccine Clinical Trials, Nanning Guangxi, China.

出版信息

Pediatr Infect Dis J. 2013 Feb;32(2):e77-81. doi: 10.1097/INF.0b013e318271c4c3.

DOI:10.1097/INF.0b013e318271c4c3
PMID:23334341
Abstract

BACKGROUND

Vaccines against hepatitis A provide long-lasting protection in both adults and children. The aim of this study was to demonstrate that the inactivated hepatitis A vaccine AVAXIM 80U Pediatric is safe and not inferior in terms of seroprotection rate to HAVRIX 720 vaccine 1 month after booster vaccination.

METHODS

An open, randomized, single-center trial was conducted in China in healthy antihepatitis A virus seronegative individuals from 12 months to 15 years of age. Participants were randomized in a 2:1 ratio to receive either AVAXIM 80U Pediatric or HAVRIX 720, followed by a booster vaccination, using the same vaccine 6 months afterward.

RESULTS

A total of 720 individuals were included in the study, 480 in the AVAXIM 80U Pediatric group and 240 in the HAVRIX 720 group, and 686 individuals completed the full vaccination schedule. AVAXIM 80U Pediatric was statistically noninferior to HAVRIX 720 in terms of seroprotection rate for all individuals and in each of 3 age groups: toddlers (12-23 months), children (2-11 years) and adolescents (12-15 years). Antihepatitis A virus geometric mean titers were significantly higher with AVAXIM 80U Pediatric than with HAVRIX 720. Both inactivated hepatitis A vaccines were well-tolerated and had a similar incidence and type of adverse events.

CONCLUSION

AVAXIM 80U Pediatric is safe and immunogenic, with a seroprotection rate that is not inferior to HAVRIX 720 in a pediatric population of healthy individuals.

摘要

背景

甲型肝炎疫苗可为成人和儿童提供持久的保护。本研究旨在证明,在加强免疫接种后 1 个月,灭活甲型肝炎疫苗 AVAXIM 80U 儿科的安全性不劣于 HAVRIX 720 疫苗,且血清保护率不低于 HAVRIX 720 疫苗。

方法

在中国进行了一项开放性、随机、单中心试验,纳入了 12 个月至 15 岁的健康抗甲型肝炎病毒血清阴性个体。参与者以 2:1 的比例随机分配接受 AVAXIM 80U 儿科或 HAVRIX 720 疫苗,随后在 6 个月后使用相同的疫苗进行加强免疫接种。

结果

共有 720 名个体纳入研究,480 名接受 AVAXIM 80U 儿科疫苗,240 名接受 HAVRIX 720 疫苗,686 名个体完成了完整的接种方案。对于所有个体和 3 个年龄组(12-23 个月的幼儿、2-11 岁的儿童和 12-15 岁的青少年),AVAXIM 80U 儿科在血清保护率方面均与 HAVRIX 720 疫苗具有统计学上的非劣效性。AVAXIM 80U 儿科的甲型肝炎病毒抗体几何平均滴度明显高于 HAVRIX 720 疫苗。两种灭活甲型肝炎疫苗均具有良好的耐受性,且不良反应的发生率和类型相似。

结论

AVAXIM 80U 儿科在健康个体的儿科人群中是安全且具有免疫原性的,其血清保护率不劣于 HAVRIX 720 疫苗。

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