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Persistence and immune memory to hepatitis B vaccine 20 y after primary vaccination of Thai infants, born to HBsAg and HBeAg positive mothers

机译:对泰国婴儿进行初次疫苗接种后20个月对HBsAg和HBeAg阳性母亲出生的乙型肝炎疫苗的持久性和免疫记忆

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This study assessed antibody persistence and immune memory to hepatitis B vaccine 20 y after priming with a recombinant hepatitis B virus (HBV) vaccine during infancy. Infants were vaccinated according to a 0, 1, 6 mo schedule with or without simultaneous administration of hepatitis B immunoglobulin (HBIg). Half of the subjects enrolled received an interim booster dose at year 5 (boosted) group, whereas the other half of the subjects enrolled did not (unboosted group). Antibody persistence was assessed until year 20. Immune memory was assessed by administration of a final HBV vaccine challenge dose at year 20 in a second study. At year 20, anti-HBs antibody concentration ≥ 10 mIU/ml rates and GMCs were higher among subjects in the boosted group (84.2% [16/19]; 95%CI: 60.4-96.6) when compared with those in the unboosted group [44.0% (11/25)]; 95% CI: 24.4-65.1). After the HBV vaccine challenge dose at year 20, anti-HBs anamnestic response for subjects in the unboosted and boosted groups was observed in 93.1% (95% CI: 77.2-99.2) and 100% (95% CI: 76.8-100) of subjects, respectively. The mean anti-HBs antibody concentration (GMC) was 562.0 mIU/ml (292.5-1079.7 mIU/ml) post administration of the challenge dose; this is a 28.5 fold increase from the pre- to post-challenge dose administration at year 20. This study demonstrates persistence of anti-HBs antibodies and presence of immune memory following hepatitis B vaccination for up to at least 20 y in Thailand. Immune memory was demonstrated for virtually all subjects, regardless whether they received they had received the additional HBV dose or not. The challenge dose at year 20 was well tolerated and a robust response was demonstrated. ClinicalTrials.gov Identifier: NCT00240526, NCT00774995.
机译:这项研究评估了婴儿期用重组乙型肝炎病毒(HBV)疫苗启动后20 y对乙型肝炎疫苗的抗体持久性和免疫记忆。按照0、1、6个月的时间表给婴儿接种疫苗,有或没有同时给予乙型肝炎免疫球蛋白(HBIg)。入选的受试者中有一半在第5年(增强)组接受了临时加强剂量,而另一半的受试者没有接受(增强组)。在第二年的研究中,评估抗体的持久性直至20年。通过在20年时施用最终的HBV疫苗激发剂量来评估免疫记忆。到第20年,加强型受试者的抗HBs抗体浓度≥10 mIU / ml和GMC高于未加强型受试者(84.2%[16/19]; 95%CI:60.4-96.6)。 [44.0%(11/25)]; 95%CI:24.4-65.1)。在第20年接受HBV疫苗激发剂量后,未增强和增强组中受试者的抗HBs记忆消除反应的发生率分别为93.1%(95%CI:77.2-99.2)和100%(95%CI:76.8-100)。分别。给予攻击剂量后,平均抗HBs抗体浓度(GMC)为562.0 mIU / ml(292.5-1079.7 mIU / ml);与从攻击前到给药后第20年的剂量相比,这一数字增加了28.5倍。这项研究表明,在泰国接种乙肝疫苗至少20年后,抗HBs抗体的持久性和免疫记忆的存在。几乎所有受试者都表现出了免疫记忆,无论他们是否接受了额外的HBV剂量。第20年的挑战剂量耐受性良好,并显示出有力的反应。 ClinicalTrials.gov标识符:NCT00240526,NCT00774995。

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