Basta Nicole E, Borrow Ray, Berthe Abdoulaye, Dembélé Awa Traoré Eps, Onwuchekwa Uma, Townsend Kelly, Boukary Rahamatou M, Mabey Lesley, Findlow Helen, Bai Xilian, Sow Samba O
Division of Epidemiology and Community Health, University of Minnesota, Minneapolis Fogarty International Center, National Institutes of Health, Bethesda, Maryland.
Vaccine Evaluation Unit, Public Health England, Manchester Royal Infirmary, United Kingdom.
Clin Infect Dis. 2015 Nov 15;61 Suppl 5(Suppl 5):S547-53. doi: 10.1093/cid/civ602.
In 2010, Africa's first preventive meningococcal mass vaccination campaign was launched using a newly developed Neisseria meningitidis group A (NmA) polysaccharide-tetanus toxoid conjugate vaccine, PsA-TT (MenAfriVac), designed specifically for the meningitis belt. Given PsA-TT's recent introduction, the duration of protection against meningococcal group A is unknown.
We conducted a household-based, age-stratified seroprevalence survey in Bamako, Mali, in 2012, 2 years after the vaccination campaign targeted all 1- to 29-year-olds. Randomly selected participants who had been eligible for PsA-TT provided a blood sample and responded to a questionnaire. Sera were analyzed to assess NmA-specific serum bactericidal antibody titers using rabbit complement (rSBA) and NmA-specific immunoglobulin G (IgG) by enzyme-linked immunosorbent assay. The proportion of participants putatively protected and the age group- and sex-specific rSBA geometric mean titers (GMTs) and IgG geometric mean concentrations (GMCs) were determined.
Two years postvaccination, nearly all of the 800 participants (99.0%; 95% confidence interval [CI], 98.3%-99.7%) maintained NmA-specific rSBA titers ≥8, the accepted threshold for protection; 98.6% (95% CI, 97.8%-99.4%) had titers ≥128, and 89.5% (95% CI, 87.4%-91.6%) had titers ≥1024. The rSBA GMTs were significantly higher in females than in males aged <18 years at vaccination (P < .0001). NmA-specific IgG levels ≥2 µg/mL were found in 88.5% (95% CI, 86.3%-90.7%) of participants.
Two years after PsA-TT introduction, a very high proportion of the population targeted for vaccination maintains high antibody titers against NmA. Assessing the duration of protection provided by PsA-TT is a priority for implementing evidence-based vaccination strategies. Representative, population-based seroprevalence studies complement clinical trials and provide this key evidence.
2010年,非洲发起了首次预防性脑膜炎球菌大规模疫苗接种运动,使用一种新开发的A群脑膜炎奈瑟菌(NmA)多糖-破伤风类毒素结合疫苗,即PsA-TT(MenAfriVac),该疫苗是专门为脑膜炎带设计的。鉴于PsA-TT是最近才引入的,其对A群脑膜炎球菌的保护持续时间尚不清楚。
在2012年,即针对所有1至29岁人群的疫苗接种运动开展两年后,我们在马里的巴马科进行了一项基于家庭的、按年龄分层的血清流行率调查。随机选择符合接种PsA-TT条件的参与者提供血样并回答问卷。使用兔补体(rSBA)分析血清以评估NmA特异性血清杀菌抗体滴度,并通过酶联免疫吸附测定法检测NmA特异性免疫球蛋白G(IgG)。确定推定受保护参与者的比例以及按年龄组和性别划分的rSBA几何平均滴度(GMT)和IgG几何平均浓度(GMC)。
疫苗接种后两年,800名参与者中几乎所有人(99.0%;95%置信区间[CI],98.3%-99.7%)维持NmA特异性rSBA滴度≥8,这是公认的保护阈值;98.6%(95%CI,97.8%-99.4%)的滴度≥128,89.5%(95%CI,87.4%-91.6%)的滴度≥1024。在接种疫苗时年龄<18岁的女性中,rSBA GMT显著高于男性(P<.0001)。88.5%(95%CI,86.3%-90.7%)的参与者中发现NmA特异性IgG水平≥2μg/mL。
引入PsA-TT两年后,很大比例的目标接种人群维持了针对NmA的高抗体滴度。评估PsA-TT提供的保护持续时间是实施循证疫苗接种策略的优先事项。具有代表性的、基于人群的血清流行率研究可补充临床试验并提供这一关键证据。