首页> 外文期刊>The Pediatric infectious disease journal >Immunogenicity and safety of a booster dose of the 10-valent pneumococcal haemophilus influenzae protein D conjugate vaccine coadministered with the tetravalent meningococcal serogroups A, C, W-135 and y tetanus toxoid conjugate vaccine in toddlers: A randomized trial
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Immunogenicity and safety of a booster dose of the 10-valent pneumococcal haemophilus influenzae protein D conjugate vaccine coadministered with the tetravalent meningococcal serogroups A, C, W-135 and y tetanus toxoid conjugate vaccine in toddlers: A randomized trial

机译:加强剂量的10价肺炎球菌流感嗜血杆菌流感病毒D蛋白结合疫苗与四价脑膜炎球菌血清群A,C,W-135和破伤风类毒素结合疫苗的幼儿:一项随机试验

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Background: This open, randomized clinical trial (NCT00758264) evaluated the coadministration of a booster dose of the 10-valent pneumococcal conjugate vaccine (PHiD-CV) and a single dose of the tetravalent meningococcal conjugate vaccine (MenACWY-TT) in Taiwanese and Mexican toddlers. Methods: Healthy toddlers aged 12-23 months (N = 363) were randomized (2:1:1) to receive either both vaccines at first visit, MenACWY-TT at first visit and 1 month later PHiD-CV, or PHiD-CV at first visit and 1 month later MenACWY-TT. Immune responses were measured 1 month after MenACWY-TT vaccination by meningococcal serum bactericidal activity (rSBA) assay and 1 month after PHiD-CV vaccination by pneumococcal 22F-inhibition enzyme-linked immunosorbent assay and functional opsonophagocytic activity assay. Solicited and unsolicited symptoms were recorded for days 4 and 31 postvaccination, respectively. Serious adverse events were recorded throughout the study. Results: The prespecified criteria for noninferiority of coadministration versus individual administrations were met for all meningococcal serogroups (in terms of percentages of toddlers with rSBA titer 8) and all vaccine pneumococcal serotypes (in terms of antibody geometric mean concentration ratios), except pneumococcal serotype 18C. For each meningococcal serogroup, 97.5% of toddlers across the 3 groups had rSBA titers 128 at 1 month after MenACWY-TT vaccination. For each pneumococcal serotype, at 1 month after PHiD-CV vaccination, 96.0% and 92.9% of toddlers across the 3 groups had antibody concentrations 0.2 μg/mL and opsonophagocytic activity titers 8, respectively. The safety profiles of both vaccines when coadministered were clinically acceptable. Conclusions: This study supports the coadministration of PHiD-CV and MenACWY-TT in toddlers.
机译:背景:这项开放的随机临床试验(NCT00758264)在台湾和墨西哥评估了加强剂量的10价肺炎球菌结合疫苗(PHiD-CV)和单价的四价脑膜炎球菌结合疫苗(MenACWY-TT)的共同给药幼儿。方法:将12-23个月(N = 363)的健康幼儿随机分配(2:1:1)以在初次就诊时,初次就诊时MenACWY-TT和在1个月后接受PHiD-CV或PHiD-CV两种疫苗首次访问时和1个月后访问MenACWY-TT。在MenACWY-TT疫苗接种后1个月,通过脑膜炎球菌血清杀菌活性(rSBA)测定,在PHiD-CV疫苗接种后1个月,通过肺炎球菌22F抑制酶联免疫吸附测定和功能性吞噬吞噬活性测定来测量免疫应答。接种后第4天和第31天分别记录了自发症状和自发症状。在整个研究中记录了严重的不良事件。结果:除18mg肺炎球菌血清型外,所有脑膜炎球菌血清群(以rSBA滴度为8的幼儿的百分比表示)和所有疫苗肺炎球菌血清型(以抗体几何平均浓度比表示)均符合预先确定的共同给药与个体给药不劣标准。 。对于每个脑膜炎球菌血清群,三组中97.5%的幼儿在MenACWY-TT疫苗接种后1个月的rSBA效价为128。对于每种肺炎球菌血清型,在PHiD-CV疫苗接种后1个月,三组中96.0%和92.9%的幼儿的抗体浓度分别为0.2μg/ mL和调理吞噬活性滴度8。两种疫苗并用时的安全性在临床上是可以接受的。结论:这项研究支持PHiD-CV和MenACWY-TT在幼儿中的共同给药。

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