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首页> 外文期刊>Trials >The effect of a single 4CMenB vaccine booster in young people more than ten years after infant immunisation: protocol of an exploratory immunogenicity study
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The effect of a single 4CMenB vaccine booster in young people more than ten years after infant immunisation: protocol of an exploratory immunogenicity study

机译:婴儿免疫后十多年的青少年单一4cmenb疫苗助力的影响:探索性免疫原性研究的议定书

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The four-component capsular group B meningococcal vaccine (4CMenB) was introduced into the national immunisation schedule in the UK in September 2015 for infants in a 2?+?1 schedule at two, four and 12?months of age. A two-dose immunisation schedule for adolescents was also considered but was not found to be cost-effective in view of the relatively low rates of disease in this age group. Uncertainty about the longevity of protection induced by the vaccine and lack of certainty about an anamnestic response in primed individuals contributed to this decision. This study is an open-label, descriptive immunogenicity analysis. Up to 113 participants will be recruited, including up to 83 children who are now aged 11?years and took part in previous trials involving the administration of 4CMenB to infants, plus a group of 30 na?ve age-matched controls. All previously immunised participants will receive one booster dose of 4CMenB. The 30 na?ve participants will be randomised to receive two doses of 4CMenB either at 0 and 28?days or 0 and 365?days. Blood samples will be collected from all participants at 0, 28, 180 and 365?days. The primary endpoint will explore immunogenicity at day 0 and 180 in previously immunised and na?ve participants. Secondary outcomes will include investigating the persistence of antibody protection in previously immunised participants at the beginning of the study, describing the characteristics of the memory B-cell responses in previously immunised participants, and measuring reactogenicity in all participants following 4CMenB doses. This study aims to describe whether or not a single booster dose of 4CMenB given to those who have received an infant course of 4CMenB induces a recall immune response, while concurrently describing immune responses in na?ve children of the same age. If an anamnestic response is proven, a single dose adolescent booster could be envisaged as an addition to the current UK vaccination schedule. EudraCT, 2017-004732-11. ISRCTN, ISRCTN16774163. Registered on 10 May 2018 (retrospectively registered).
机译:2015年9月,在英国的国家免疫表中,为2次婴儿,在英国的国家免疫表中引入了四分组分囊组疫苗(4cmeNb)。考虑到这一年龄组中疾病率相对较低的疾病率,还没有发现青少年的双剂量免疫时间表。关于疫苗诱导的寿命的不确定性,缺乏关于灌注个人在灌注个人中缺乏确定性的不确定性导致了这一决定。本研究是一种开放标签,描述性免疫原性分析。最多113名参与者将被招募,包括高达83名现在的儿童11岁?年龄较少,并参加以前的试验,涉及4CMENB给婴儿的审判,以及一组30个Na ve的年龄匹配的控制。所有以前免疫的参与者将获得一个助推剂量为4cmenb。 30 Na'Ve参与者将随机化,以在0和28℃下接受两剂4cmenb?天或0和365?天。将从所有参与者收集血样,在0,28,180和365?天的所有参与者中收集。主要终点将在先前免疫的和NA ve参与者中探讨第0天和第180天的免疫原性。二次结果将包括在研究开始,研究先前免疫的参与者在研究开始的抗体保护的持续性,描述了先前免疫的参与者中的记忆B细胞应答的特征,以及在4cmenb剂量后的所有参与者中测量反应性。本研究旨在描述4CMENB的单个增强剂量给予那些接受4CMENB的婴儿疗程的人诱导召回免疫反应,同时描述同龄人类的Na've儿童中的免疫反应。如果经过验证的,可以设想单剂量青少年助推器,作为当前英国疫​​苗接种时间表的添加。 eudract,2017-004732-11。 ISRCTN,ISRCTN16774163。 2018年5月10日注册(回顾性地注册)。

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