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首页> 外文期刊>BMC Infectious Diseases >Safety and immunogenicity of a freeze-dried, Vero cell culture-derived, inactivated Japanese encephalitis vaccine (KD-287, ENCEVAC?) versus a mouse brain-derived inactivated Japanese encephalitis vaccine in children: a phase III, multicenter, double-blinded, randomized trial
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Safety and immunogenicity of a freeze-dried, Vero cell culture-derived, inactivated Japanese encephalitis vaccine (KD-287, ENCEVAC?) versus a mouse brain-derived inactivated Japanese encephalitis vaccine in children: a phase III, multicenter, double-blinded, randomized trial

机译:冷冻干燥,Vero细胞培养衍生的灭活日本脑炎疫苗(KD-287,ENCEVAC?)与小鼠脑源灭活的日本脑炎疫苗在儿童中的安全性和免疫原性:III期,多中心,双盲,随机试验

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Background Although mouse brain-derived, inactivated Japanese encephalitis vaccines (JE-MBs) have been successfully used for a long time, potential rare neurological complications have prompted the development of a Vero cell culture-derived inactivated vaccine (JE-VC). In a phase III clinical study, we aimed to compare the safety and immunogenicity of a JE-VC, KD-287 with a JE-MB, JEV-GCC, in children. Methods In this multicenter, double-blinded, randomized controlled trial, the study population consisted of 205 healthy Korean children aged 12–23 months. Each subject was subcutaneously vaccinated with either KD-287 or JEV-GCC twice at an interval of 2?weeks and then vaccinated once 12?months after the second vaccination. Neutralizing antibodies were measured by the plaque reduction neutralization test using the homologous and heterologous, as a post hoc analysis, challenge virus strains. Results The three-dose regimen of KD-287 showed a comparable safety profile with JEV-GCC except higher incidence of fever after the first dose (30.4% and 14.7%, respectively). Most of the fever was mild degree (61.3% and 66.7%, respectively). KD-287 fulfilled the non-inferiority criteria for seroconversion rate (SCR) and geometric mean titer (GMT) of the neutralizing antibody, which were the primary endpoints, at 4?weeks after the third vaccination (95% CI: ?1.00, 3.10 for the SCR difference and 10.8, 17.6 for the GMT ratio). The SCRs of KD-287 were all 100% and the GMTs were higher in the KD-287 group than in the JEV-GCC group after the second vaccination and before and after the third vaccination (GMT ratio: 5.59, 20.13, and 13.79, respectively, p?p? Conclusions This study suggests that the KD-287, a JE-VC is as safe as and may be more effective than the licensed MB-derived vaccine. KD-287 could thus be useful as a second-generation vaccine and substitute for the current JE-MB vaccine in Korean children. Trial registration ClinicalTrials.gov: NCT01150942 webcite
机译:背景技术尽管小鼠脑源灭活的日本脑炎疫苗(JE-MBs)已成功使用了很长时间,但潜在的罕见神经系统并发症却促使开发了Vero细胞培养源灭活疫苗(JE-VC)。在III期临床研究中,我们旨在比较JE-VC,KD-287与JE-MB,JEV-GCC在儿童中的安全性和免疫原性。方法在这项多中心,双盲,随机对照试验中,研究人群包括205名12-23个月大的健康韩国儿童。每位受试者在2周的间隔内两次接受KD-287或JEV-GCC皮下接种,然后在第二次接种后12个月进行一次疫苗接种。通过噬斑减少中和测试,使用同源和异源,作为事后分析,挑战病毒株,通过中和抗体来测量中和抗体。结果KD-287的三剂量方案显示出与JEV-GCC相当的安全性,只是在第一剂后发烧的发生率更高(分别为30.4%和14.7%)。大部分发烧是轻度的(分别为61.3%和66.7%)。 KD-287在第三次接种后4周达到了中和性抗体的血清转化率(SCR)和几何平均滴度(GMT)的非劣效性标准,这是主要终点(95%CI:≥1.00,3.10) SCR差异为10.8,GMT比为17.6)。在第二次接种后,第三次接种前后,KD-287组的KD-287的SCR均为100%,GMT高于JEV-GCC组(GMT比率:5.59、20.13和13.79,结论本研究表明,JE-VC KD-287与获得许可的MB衍生疫苗一样安全,并且可能更有效,因此,KD-287可用作第二代疫苗并替代目前在韩国儿童中使用的JE-MB疫苗试用注册ClinicalTrials.gov:NCT01150942网站

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