Thornton V, Lennon D, Rasanathan K, O'Hallahan J, Oster P, Stewart J, Tilman S, Aaberge I, Feiring B, Nokleby H, Rosenqvist E, White K, Reid S, Mulholland K, Wakefield M J, Martin D
The University of Auckland, Meningococcal B Project, P.O. Box 98847, South Auckland Mail Centre, Auckland, New Zealand.
Vaccine. 2006 Feb 27;24(9):1395-400. doi: 10.1016/j.vaccine.2005.09.043. Epub 2005 Oct 4.
As the first step towards control of a strain specific epidemic of meningococcal disease in New Zealand (NZ), this study, an observer-blind, randomised controlled trial in 75 healthy adults, evaluated safety and immunogenicity of two different dosages of a meningococcal group B vaccine administered in a three dose regime. The "tailor-made" outer membrane vesicle (OMV) vaccine (candidate vaccine) developed using a New Zealand meningococcal group B strain (B:4:P1.7b,4) was well tolerated with no vaccine related serious adverse events. Similar local and systemic reactions were observed in those receiving the New Zealand candidate vaccine and the control parent Norwegian vaccine (MenBvac). A four-fold rise in serum bactericidal antibodies (SBAb) against the vaccine strain 4-6 weeks after the third vaccination was achieved in 100% of New Zealand candidate vaccine 2,519 microg participants and in 87% of 50 microg participants. The safety and immunogenicity profile observed in this study of healthy adults enabled studies in children to be initiated using 25 microg dosage.
作为在新西兰(NZ)控制特定菌株的脑膜炎球菌病流行的第一步,本研究是一项针对75名健康成年人的观察者盲法随机对照试验,评估了以三剂方案接种的两种不同剂量的B群脑膜炎球菌疫苗的安全性和免疫原性。使用新西兰B群脑膜炎球菌菌株(B:4:P1.7b,4)研制的“定制”外膜囊泡(OMV)疫苗(候选疫苗)耐受性良好,未出现与疫苗相关的严重不良事件。接受新西兰候选疫苗和对照亲本挪威疫苗(MenBvac)的人群中观察到了相似的局部和全身反应。在第三次接种疫苗4 - 6周后,100%的2519微克新西兰候选疫苗接种者和87%的50微克接种者血清杀菌抗体(SBAb)针对疫苗菌株出现了四倍增长。本研究在健康成年人中观察到的安全性和免疫原性特征使得能够启动针对儿童的25微克剂量研究。