一项随机、双盲、主动对照的III期试验,在6个月至18岁的健康韩国儿童和青少年中使用细胞培养衍生的四价灭活流感疫苗。

B. Eun, T. Lee, Jina Lee, Ki Hwan Kim, Dong Ho Kim, D. Jo, S. Shin, Hun Kim, Kyung-Ho Kim, Y. Kim
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引用次数: 6

摘要

与基于鸡蛋的流感疫苗相比,细胞培养衍生的流感疫苗具有几个重要的优势。四价流感疫苗比三价流感疫苗多含有1个B型毒株,可提供更广泛的季节性流感保护。本研究的目的是评估一种新型细胞培养衍生的灭活四价流感疫苗(cIIV4) NBP607-QIV在儿童和青少年中的免疫原性和安全性。该III期、随机、双盲、多中心试验于2014-2015年在韩国进行,研究对象为儿童/青少年(6个月至18岁)。受试者按4:1随机接种NBP607-QIV或对照灭活三价流感疫苗。在接种前和接种后28天血清中评估血凝抑制抗体滴度。收集疫苗接种后6个月的安全性数据。结果共有454名参与者完成了研究。366名受试者接种了cIIV4, 88名受试者接种了三价灭活流感疫苗。总体而言,NBP607-QIV均符合人用药品委员会的免疫原性标准。在NBP607-QIV和对照组之间,免疫原性终点具有可比性。在NBP607-QIV和对照组中,年龄小于3岁的参与者对2种乙型流感毒株的免疫反应较低。没有死亡、疫苗相关严重不良事件(ae)或因ae而停药的报告。征求的ae报告一般为轻度强度。结论snbp607 - qiv是一种新型的cIIV4,对4种流感毒株均具有良好的免疫原性,在儿童和青少年中具有可耐受的安全性。此外,NBP607-QIV对乙型流感的免疫原性比对照(一种基于鸡蛋的亚单位疫苗)更强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Randomized, Double-blind, Active-controlled Phase III Trial of a Cell Culture-derived Quadrivalent Inactivated Influenza Vaccine in Healthy South Korean Children and Adolescents 6 Months to 18 Years of Age.
BACKGROUND Cell culture-derived influenza vaccines have several important advantages over egg-based influenza vaccines. The quadrivalent influenza vaccine may offer broader protection against seasonal influenza than trivalent influenza vaccine by containing 1 more B strain. The purpose of this study was to evaluate the immunogenicity and safety of NBP607-QIV, a novel cell culture-derived inactivated quadrivalent influenza vaccine (cIIV4), in children and adolescents. METHODS This phase III, randomized, double-blind, multicenter trial in children/adolescents (6 mo to 18 yr) was conducted in South Korea during 2014-2015 season. Subjects were randomized 4:1 to receive either NBP607-QIV or control inactivated trivalent influenza vaccine. Hemagglutination inhibition antibody titers were assessed in prevaccination and 28 days postvaccination sera. Safety data were collected for up to 6 months postvaccination. RESULTS A total of 454 participants completed the study. Three-hundred sixty-six subjects received cIIV4 and 88 subjects received inactivated trivalent influenza vaccine. Overall, NBP607-QIV met the immunogenicity criteria of Committee for Medicinal Products for Human Use for each of the 4 strains. Between the NBP607-QIV and control groups, immunogenicity endpoints were comparable. Participants younger than 3 years of age had lower immunologic responses to 2 influenza B strains in both NBP607-QIV and control group. No deaths, vaccine-related serious adverse events (AEs) or withdrawals because of AEs were reported. The solicited AEs reported were generally of mild intensity. CONCLUSIONS NBP607-QIV, a novel cIIV4, showed good immunogenicity to all 4 influenza strains and had tolerable safety profiles in children and adolescents. Moreover, NBP607-QIV was more immunogenic against influenza B compared to the control, an egg-based subunit vaccine.
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