Trotter Caroline, Findlow Jamie, Balmer Paul, Holland Ann, Barchha Rita, Hamer Nick, Andrews Nick, Miller Elizabeth, Borrow Ray
Department of Social Medicine, University of Bristol, Canynge Hall, Whiteladies Road, Bristol BS8 2PR, United Kingdom.
Clin Vaccine Immunol. 2007 Jul;14(7):863-8. doi: 10.1128/CVI.00102-07. Epub 2007 May 9.
Outer membrane vesicle (OMV) and recombinant protein-based vaccines targeted against multiple strains of group B meningococci are under development. The serum bactericidal antibody (SBA) assay has been designated the surrogate of protection, but the exact cutoff has not been determined. We measured the SBA titers in 2,415 serum samples and the anti-OMV IgG antibody concentrations in 2,672 serum samples representative of the English population to establish a baseline of natural immunity. SBA and anti-OMV IgG antibody titers are high in infants in the first 3 months of life, declining thereafter, presumably as maternal immunity wanes. About 6% of the subjects in the 1- to 11-year-old age group had SBA titers >or=4. During the teenage years, there was a marked increase in the percentage of subjects with SBA titers >or=4, rising to over 50% in 19-year-olds, with about 20% of older adults achieving this titer. The peak in SBA and anti-OMV IgG titers coincided with the peak in meningococcal carriage. Simple mathematical models confirm that the relationship between observed seroprevalence and carriage by age is consistent with carriage inducing SBA and that following an episode of carriage, SBA levels may remain elevated for many months. With the exception of children aged 3 to 11 months, there was no clear relationship between disease incidence and seroprevalence.
针对B群脑膜炎球菌多种菌株的外膜囊泡(OMV)疫苗和基于重组蛋白的疫苗正在研发中。血清杀菌抗体(SBA)检测已被指定为保护作用的替代指标,但确切的临界值尚未确定。我们检测了2415份血清样本中的SBA滴度以及2672份代表英国人群的血清样本中的抗OMV IgG抗体浓度,以建立自然免疫的基线。SBA和抗OMV IgG抗体滴度在出生后前3个月的婴儿中较高,此后下降,推测是由于母体免疫力减弱。1至11岁年龄组中约6%的受试者SBA滴度≥4。在青少年时期,SBA滴度≥4的受试者百分比显著增加,19岁时升至50%以上,约20%的老年人达到该滴度。SBA和抗OMV IgG滴度的峰值与脑膜炎球菌携带率的峰值一致。简单的数学模型证实,观察到的血清阳性率与年龄携带率之间的关系与携带诱导SBA一致,并且在一次携带事件后,SBA水平可能会持续升高数月。除3至11个月大的儿童外,疾病发病率与血清阳性率之间没有明显关系。