Service des Maladies Infectieuses et Tropicales, Rouen, France.
Vaccine. 2012 Jul 20;30(34):5059-62. doi: 10.1016/j.vaccine.2012.05.051. Epub 2012 May 30.
A meningococcal B:14:P1.7,16 outbreak in Normandy (France) was recently controlled using MenBvac, an outer membrane vesicle vaccine previously designed against the B:15:P1.7,16 strain. The further emergence of a new B:14:P1.7,16 outbreak in another district in Normandy led us to explore immunity against B:14:P1.7,16 before and after the MenBvac campaign using a 2+1 (day 0, week 6, month 8) schedule. Children (1-5 years) were sampled before, during and up to one year after vaccination. Serum bactericidal activity against B:14:P1.7,16 was titrated using human complement (hSBA) and immune response was defined by hSBA titer ≥4 as a surrogate for protection. The percentage of hSBA titer ≥4 was 10.8% before vaccination, raised to 84.1% 6 weeks after the completion of the schedule, but declined to 39.7% one year later. This level is lower than the targeted 60% level and suggests only short-term persistence of response against B:14:P1.7,16 using this schedule.
近期,在法国诺曼底(Normandy),一种针对 B:14:P1.7,16 血清型的脑膜炎奈瑟球菌 B 型疫苗(MenBvac)有效控制了 B:14:P1.7,16 血清型的爆发。在诺曼底的另一个地区,新的 B:14:P1.7,16 爆发再次出现,促使我们使用 2+1(第 0 天、第 6 周和第 8 月)的免疫程序,探索接种 MenBvac 前后针对 B:14:P1.7,16 的免疫情况。我们在接种前、接种期间和接种后一年,对 1-5 岁儿童进行了采样。采用人源补体(hSBA)测定血清杀菌活性,hSBA 滴度≥4 定义为免疫应答,作为保护的替代指标。接种前 hSBA 滴度≥4 的百分比为 10.8%,免疫程序完成 6 周后上升至 84.1%,但一年后下降至 39.7%。这一水平低于目标 60%,表明使用该免疫程序针对 B:14:P1.7,16 的反应仅能持续短期。