Characterization of Canadian Neisseria meningitidis serogroup B isolates and factor-H binding protein expression, data from the Canadian Immunization Monitoring Program Active (IMPACT), 2013–2020

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2025-03-30 DOI:10.1016/j.vaccine.2025.127030
Kevin Meesters , Manish Sadarangani , Stephen A. Clark , Ray Borrow , Raymond S.W. Tsang , Nicole Le Saux , Scott A. Halperin , Taj Jadavji , Shaun K. Morris , Julie A. Bettinger , For the members of the Canadian Immunization Monitoring Program Active (IMPACT)
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Abstract

Background

Invasive meningococcal disease, caused by Neisseria meningitidis, remains a significant health threat. This study examined the genetic diversity of serogroup B (NmB) organisms and assessed the potential coverage offered by the MenB-FHbp vaccine, licensed for individuals aged 10–25 years. NmB vaccines have not yet been incorporated into most routine immunization programs in Canada, with the exception of campaigns to deal with specific outbreaks and targeted vaccination efforts for at-risk groups.

Methods

From 2013 to 2020, NmB strains causing invasive meningococcal disease were collected through the Canadian Immunization Monitoring Program ACTive surveillance network. Each isolate underwent analysis to determine clonal complex (CC) and factor-H binding protein peptide (fHbp), and fHbp surface expression using the Meningococcal Antigen Surface Expression (MEASURE) assay.

Results

Of 119 isolates analyzed, 118 coded for full-length fHbp. CC-269 (48 isolates) and CC-41/44 (42 isolates) represented 75.6 % of all isolates. fHbp peptide 15 was the most prevalent peptide up until 2015 (47.4–53.9 %) but declined to 0–22.1 % afterwards. Median fHbp surface expression overall was 4270 MFI (IQR 2132–14,462). Peptides 15 and 210 (both CC-269) had the highest fHbp surface expression: peptide 15 (median: 18,446, IQR: 14,462–22,170) and peptide 210 (median: 28,306, IQR 24,935–31,678). Notably, 90.8 % of isolates had fHbp surface expression at a level associated with MenB-FHbp protection.

Conclusion

CC-269 and CC-41/44 predominated in 2013–2020. Notably, peptide 15, the most prevalent until 2015, declined significantly thereafter. The majority of isolates expressed fHbp at a level associated with vaccine-induced protection. A wider age authorization for the vaccine may result in increased prevention of NmB disease.
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2013-2020年加拿大脑膜炎奈瑟菌血清B组分离株特征和因子h结合蛋白表达,数据来自加拿大免疫监测计划活动(IMPACT)
背景:由脑膜炎奈瑟菌引起的侵袭性脑膜炎球菌病仍然是一个重大的健康威胁。本研究检查了血清B群(NmB)生物的遗传多样性,并评估了MenB-FHbp疫苗(许可用于10-25岁的个体)提供的潜在覆盖率。除了应对特定疫情的运动和针对高危人群的有针对性的疫苗接种工作外,加拿大大多数常规免疫规划尚未纳入NmB疫苗。方法2013 - 2020年,通过加拿大免疫监测计划ACTive监测网络收集引起侵袭性脑膜炎球菌病的NmB菌株。对每个分离株进行克隆复合体(CC)和因子- h结合蛋白肽(fHbp)的分析,并使用脑膜炎球菌抗原表面表达(MEASURE)法检测fHbp表面表达。结果119株分离株中,有118株编码全长fHbp。CC-269(48株)和CC-41/44(42株)占总分离株的75.6%。到2015年,fHbp肽15是最流行的肽(47.4% ~ 53.9%),但之后下降到0 ~ 22.1%。fHbp表面表达的中位数为4270 MFI (IQR为2132 - 14462)。肽15和210(均为CC-269)具有最高的fHbp表面表达量:肽15(中位数:18,446,IQR: 14,462 - 22170)和肽210(中位数:28,306,IQR 24,935-31,678)。值得注意的是,90.8%的分离株具有与MenB-FHbp保护相关的fHbp表面表达水平。结论2013-2020年以cc -269和CC-41/44为主。值得注意的是,肽15在2015年之前是最流行的,此后大幅下降。大多数分离株表达fHbp的水平与疫苗诱导的保护作用相关。更广泛的疫苗接种年龄可能会增加NmB疾病的预防。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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