首页> 外文OA文献 >Five-year antibody persistence and safety after a single dose of combined Haemophilus influenzae Type B Neisseria meningitidis Serogroup C-tetanus toxoid conjugate vaccine in Haemophilus influenzae Type B-primed toddlers
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Five-year antibody persistence and safety after a single dose of combined Haemophilus influenzae Type B Neisseria meningitidis Serogroup C-tetanus toxoid conjugate vaccine in Haemophilus influenzae Type B-primed toddlers

机译:单剂量联合流感嗜血杆菌B型脑膜炎奈瑟菌血清C型破伤风类毒素结合疫苗在B型流感嗜血杆菌中的5年抗体持久性和安全性

摘要

Background: Antibody persistence is evaluated in healthy Australian children 4 and 5 years postvaccination with a single dose of combined Haemophilus influenzae type b-Neisseria meningitidis serogroup C tetanus toxoid conjugate vaccine (Hib-MenC-TT) compared with separately administered Hib-TT and MenC-CRM197 vaccines (Hib + MCC). Methods: This is another follow-up of a phase III, open, randomized, controlled study (NCT00326118), in which 433 Hib-primed but MenC naïve toddlers aged 12-18 months were randomized 3:1 to receive Hib-MenC-TT or Hib + MCC vaccines. Protection against (1) MenC was measured by serum bactericidal antibody assay using rabbit complement (rSBA) and (2) Hib was measured by enzyme-linked immunosorbent assay of antibodies to polyribosylribitol phosphate (anti-PRP). Study children were assessed for any potentially vaccine-related serious adverse events at each persistence study visit. Results: The according-to-protocol cohorts for persistence at years 4 and 5 included 282 and 263 children, respectively. The percentages of children with rSBA-MenC titers ≥1:8 at years 4 and 5 were 12.5% and 19.0%, respectively, in the Hib-MenC group; and 12.3% and 25.0% in the Hib + MCC group. All children in each group had anti-PRP concentrations ≥0.15 μg/mL at year 5. Exploratory analyses suggested no potential differences between groups in rSBA-MenC or anti-PRP antibody persistence. No vaccine-related serious adverse events were reported. Conclusions: Antibody persistence was similar for years 4 and 5 after Hib-MenC-TT or Hib + MCC vaccination, with the majority of children retaining anti-PRP antibody concentrations ≥0.15 μg/mL at both timepoints. The percentage of children retaining rSBA-MenC titers ≥1:8 was low (≤25%), suggesting that a MenC booster dose may be warranted before adolescence.
机译:背景:与单独接种Hib-TT和MenC相比,在接种疫苗后4和5岁的健康澳大利亚儿童中,单剂量联合使用的流感嗜血杆菌b型脑膜炎奈瑟氏球菌血清C型破伤风类毒素结合疫苗(Hib-MenC-TT)评估了抗体的持久性-CRM197疫苗(Hib + MCC)。方法:这是第三阶段,开放,随机,对照研究(NCT00326118)的另一项随访研究,其中将433名Hib初诊但年龄在12-18个月的MenC天真的幼童随机3:1接受Hib-MenC-TT或Hib + MCC疫苗。对(1)MenC的保护作用是通过兔补体(rSBA)进行的血清杀菌抗体测定和(2)通过对多核糖基核糖醇磷酸酯的抗体(抗PRP)的酶联免疫吸附测定来测定Hib。在每次持续性研究访问中,对研究儿童进行任何可能的疫苗相关严重不良事件评估。结果:根据协议在4岁和5岁持续存在的队列分别包括282和263名儿童。在Hib-MenC组中,rSBA-MenC滴度≥1:8的儿童在4岁和5岁时的百分比分别为12.5%和19.0%。在Hib + MCC组中分别为12.3%和25.0%。每组的所有儿童在第5年的抗PRP浓度均≥0.15μg/ mL。探索性分析表明,rSBA-MenC或抗PRP抗体的持久性在各组之间无潜在差异。没有报告与疫苗相关的严重不良事件。结论:Hib-MenC-TT或Hib + MCC疫苗接种后第4年和第5年的抗体持久性相似,大多数儿童在两个时间点的抗PRP抗体浓度均保持≥0.15μg/ mL。保留rSBA-MenC滴度≥1:8的儿童的比例很低(≤25%),这表明在青春期之前有必要增加MenC的剂量。

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