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Immune response to an indigenously developed r-Hepatitis B vaccine in mixed population: Study of an accelerated vaccination schedule

机译:混合人群对本地开发的乙型肝炎乙型肝炎疫苗的免疫反应:加速接种时间表的研究

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摘要

AIM: To establish the safety and efficacy of an indigenously developed r-hepatitis B vaccine using an accelerated schedule and to highlight the social awareness and commitment in preventing the spreading of hepatitis B virus infection.METHODS: The study was a multicentric, double blind, randomized (3:1) study using three doses of vaccine immunization schedule (20 μg for those above 10 years old and 10 μg for those below 10 years old) on d 0, 30 and 60. One hundred and sixty-six subjects were enrolled (87 males and 76 females aged 5-35 years). The main outcome measure was assessment of immunogenicity and safety.RESULTS: A 100% seroconversion response was observed on the 30th d after the 1st injection in both the experimental groups. The sero-protection data reported a 41.2-65.6% response on the 30th d after the 1st injection and reached 100% on the 60th d. Descriptive statistical analysis showed a geometric mean titer value of 13.77 mIU/mL in the test (BEVAC) group and 10.95 mIU/mL in the commercial control (ENGERIX-B) group on the 30th d after the 1st injection. The response on the 60th d showed a geometric mean titre value (GMT) of 519.84 mIU/mL in the BEVAC group and 475.46 mIU/mL in the ENGERIX-B group. On the 90th d, the antibody titer response was observed to be 2627.58 mIU/mL in the BEVAC group and 2272.72 mIU/mL in the ENGERIX-B group. Two subjects in each group experienced pains at injection site after the first vaccination. A total of six subjects in both groups experienced a solicited adverse reaction, which included pains, swelling and redness at the injection site, three subjects in the group-B had a pain at the injection site after the third dose. No other serious adverse events occurred and no dose-related local or general symptoms were observed during the study.CONCLUSION: The vaccine is safe, efficacious and immunogenic in comparison with the well documented ENGERIX-B.
机译:目的:以加速的时间表确定本土研发的乙型肝炎疫苗的安全性和有效性,并强调社会对预防乙型肝炎病毒感染扩散的认识和承诺。方法:这项研究是多中心,双盲,在第0、30和60天使用三剂疫苗免疫方案(10岁以上者为20μg,10岁以下者为10μg)进行随机(3:1)研究。共纳入166名受试者。 (男性年龄为5-35岁,男性为87位,女性为76位)。结果:两个实验组在第一次注射后的第30天观察到100%的血清转化反应。血清保护数据报告,在注射1次后的第30天,应答率为41.2-65.6%,在第60次后达到100%。 > d。描述性统计分析显示,测试后(BEVAC)组在第30天后的几何平均滴度为13.77 mIU / mL,商业对照组(ENGERIX-B)组为10.95 mIU / mL。 1 st 注入。在第60天的反应显示,BEVAC组的几何平均滴度(GMT)为519.84 mIU / mL,而ENGERIX-B组的为475.46 mIU / mL。在第90天,在BEVAC组中观察到抗体滴度响应为2627.58 mIU / mL,而在ENGERIX-B组中观察到抗体滴度响应为2272.72 mIU / mL。初次接种疫苗后,每组两名受试者在注射部位感到疼痛。两组中总共有六名受试者经历了引起的不良反应,包括注射部位的疼痛,肿胀和发红,B组中的三名受试者在第三剂注射后出现了注射部位的疼痛。在研究过程中,未发生其他严重的不良事件,也未观察到剂量相关的局部或一般症状。结论:与充分证明的ENGERIX-B相比,该疫苗安全,有效和具有免疫原性。

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