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首页> 外文期刊>Vaccine >Serum bactericidal activity correlates with the vaccine efficacy of outer membrane vesicle vaccines against Neisseria meningitidis serogroup B disease
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Serum bactericidal activity correlates with the vaccine efficacy of outer membrane vesicle vaccines against Neisseria meningitidis serogroup B disease

机译:血清杀菌活性与外膜囊泡疫苗针对B型脑膜炎奈瑟菌的疫苗效力有关

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For evaluation of serum bactericidal activity (SBA) as surrogate for the efficacy of outer membrane vesicle (OMV) vaccines against Neisseria meningitidis serogroup B disease, we have reanalyzed data from a randomized double blind placebo-controlled efficacy trial involving 172,000 secondary school students (aged 13-14 years) in Norway (1988-1991). A cohort of the efficacy trial consisting of 880 individuals was selected for immunogenicity studies. An efficacy of 87% was calculated for a 10-month observation period. However, after an observation period of 29 months, the estimated efficacy against group B disease induced by vaccination was 57%. The immunogenicity study showed that the SBA geometric mean titer (GMT) for the vaccinees was 2.4 before vaccination and 19.0 six weeks after the second vaccine dose. One year after vaccination the GMT was reduced to 2.8. A separate three-dose study with 304 adolescents showed that with a third dose at 10 months after the second dose (i.e. when cases of disease started to appear) a strong booster response was induced. Ten months after the second dose the SBA was reduced to near pre-immunization level. Following the third dose the SBA geometric mean titer of 2.7 increased to 62.3. One year after the third dose, the GMT was markedly higher than 6 weeks after the second dose (12.6 versus 8.8). Thus, protection after vaccination corresponds with the level of SBA. In order to reach lasting protective levels of SBA in a population, three vaccine doses are probably required. Measurements of SBA are likely to be useful for evaluating various upcoming formulations and improvements of immunization regimens for OMV vaccines.
机译:为了评估血清杀菌活性(SBA)作为替代外膜囊泡(OMV)疫苗对抗脑膜炎奈瑟球菌B血清型疾病的功效的替代方法,我们重新分析了一项涉及172,000名中学生(年龄较大)的随机双盲安慰剂对照功效试验的数据13-14岁)在挪威(1988-1991年)。选择了一个由880名个体组成的功效试验队列用于免疫原性研究。在10个月的观察期内,计算得出的功效为87%。然而,在29个月的观察期后,估计的针对疫苗接种引起的B组疾病的疗效为57%。免疫原性研究表明,疫苗接种者的SBA几何平均滴度(GMT)在接种前为2.4,在第二次接种后六周为19.0。接种疫苗一年后,格林尼治标准时间降至2.8。另一项针对304名青少年的三剂研究表明,在第二剂之后10个月(即当疾病病例开始出现时)服用第三剂,会产生强烈的加强免疫反应。第二次给药后十个月,SBA降低到接近免疫前水平。第三次注射后,SBA的几何平均滴度为2.7,增至62.3。第三次给药后一年,GMT明显高于第二次给药后6周(12.6对8.8)。因此,疫苗接种后的保护与SBA的水平相对应。为了达到人群中SBA的持久保护水平,可能需要三剂疫苗。 SBA的测量可能对评估各种即将到来的制剂以及OMV疫苗免疫方案的改进很有用。

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