首页> 美国卫生研究院文献>Human Vaccines Immunotherapeutics >A randomized controlled blinded study of the safety immunogenicity and batch consistency of Aleph inactivated split influenza vaccine made in China in Chinese people
【2h】

A randomized controlled blinded study of the safety immunogenicity and batch consistency of Aleph inactivated split influenza vaccine made in China in Chinese people

机译:中国制造的中国人Aleph灭活分裂流感疫苗的安全性免疫原性和批次一致性的随机对照盲法研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

To evaluate the safety, immunogenicity and batch consistency of Aleph inactivated split influenza vaccine, 3308 healthy Chinese people more than 3 years old were enrolled in a randomized, controlled, blinded study and divided into four age groups: 3–10 years, 11–17 years, 18–54 years, and more than 55 years. Each age group was then randomized (2:1) to receive either influenza vaccine or control vaccine (recombinant hepatitis B) for one dose. Also each influenza vaccine group was randomized (1:1:1) to receive three different batches of influenza vaccine. Systematic and local adverse reactions for 28 days after vaccination were recorded, and influenza antibody titer was determined by hemagglutination inhibition (HI) assay at 28 days after vaccination. There were significant differences in seroconversion and seroprotection rates achieved post-immunization of three strains of influenza antibody (H1N1, H3N2, B) between experimental group and control group in all age groups (P < 0.05). In addition, there were no statistically significant differences in local and systematic reaction rates after vaccination between the experimental and control group in all age groups (P > 0.05), except for the systematic reaction rates in the 18–54 years and ≥ 55 years age groups (P < 0.05). Thus, Aleph inactivated split influenza vaccine has good safety and immunogenicity.
机译:为了评估Aleph灭活的分裂流感疫苗的安全性,免疫原性和批次一致性,我们对3308名3岁以上的健康中国人进行了一项随机,对照,盲法研究,分为4个年龄段:3-10岁,11-17年,18-54年以及超过55年。然后将每个年龄组随机(2:1)接受一剂流感疫苗或对照疫苗(重组乙型肝炎)。每个流感疫苗组也被随机分配(1:1:1:1)以接受三批不同的流感疫苗。记录接种后28天的全身和局部不良反应,并在接种后28天通过血凝抑制(HI)分析测定流感病毒抗体滴度。在所有年龄段的实验组和对照组之间,三种流感病毒株(H1N1,H3N2,B)的免疫后血清转化率和血清保护率均存在显着差异(P <0.05)。此外,除18-54岁和≥55岁年龄段的系统反应率外,所有年龄段的实验组和对照组之间,疫苗接种后局部和系统反应率的差异均无统计学意义(P> 0.05)。组(P <0.05)。因此,Aleph灭活的分裂流感疫苗具有良好的安全性和免疫原性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号