Harrison Robyn, Stirling Robert, Baclic Oliver, Vaudry Wendy
NACI Meningococcal Disease Working Group Chair.
University of Alberta, Edmonton, AB.
Can Commun Dis Rep. 2020 Feb 6;46(2-3):36-39. doi: 10.14745/ccdr.v46i23a03.
TrumenbaTM, a bivalent, factor-H binding protein meningococcal serogroup B (MenB-fHBP) vaccine was authorized for use in Canada in October 2017 for the prevention of invasive meningococcal disease (IMD) caused by serogroup B in individuals 10-25 years of age. The National Advisory Committee on Immunization (NACI) provides recommendations regarding the use of meningococcal vaccines to the Public Health Agency of Canada.
To summarize NACI recommendations regarding the use of MenB-fHBP vaccine in Canada.
The NACI Meningococcal Disease Working Group developed a predefined search strategy to identify all eligible studies, assessed the quality of these studies, and summarized and analyzed the findings. According to the NACI evidence-based process, the working group then proposed recommendations and identified the grade of evidence that supported them. In light of the evidence, the recommendations were then considered and approved by NACI.
The two serogroup B meningococcal vaccines currently authorized for use in Canada are not interchangeable as they contain different antigens and there are no published studies on the immunogenicity resulting from a vaccination series combining the two products. Following the review of evidence, NACI recommends that MenB-fHBP vaccine may be considered as an option for use in individuals 10 years of age and older in situations when a serogroup B meningococcal vaccine should be offered: 1) during serogroup B meningococcal disease outbreaks or with the emergence of hyperendemic strains that are predicted to be susceptible to the vaccine; 2) for individuals who are close contacts with a case of invasive meningococcal disease caused by serogroup B ; 3) for individuals with underlying medical conditions that would put them at higher risk of meningococcal disease than the general population; or 4) for individuals at higher risk of exposure to serogroup B meningococcal isolates than the general population. NACI also recommends that MenB-fHBP vaccine may be considered as an option for individuals 10-25 years of age who are not at higher risk of meningococcal disease than the general population, but who wish to reduce their risk of invasive serogroup B meningococcal disease.
NACI recommends immunization against serogroup B IMD for all individuals who are at a higher risk of disease due to an underlying medical condition or an increased risk of exposure. In addition to providing guidance to public health decision-makers (i.e. provinces/territories making decisions for publicly-funded immunization programs), these NACI recommendations provide information to individuals, vaccine providers and organizations about vaccines that may not currently be included in publicly funded immunization programs. NACI continues to recommend against the use of the serogroup B vaccines in routine universal immunization programs in Canada at this time.
TrumenbaTM是一种二价、结合因子H的B群脑膜炎球菌(MenB-fHBP)疫苗,于2017年10月在加拿大获得批准,用于预防10至25岁人群中由B群引起的侵袭性脑膜炎球菌病(IMD)。国家免疫咨询委员会(NACI)就脑膜炎球菌疫苗的使用向加拿大公共卫生署提供建议。
总结NACI关于在加拿大使用MenB-fHBP疫苗的建议。
NACI脑膜炎球菌病工作组制定了预定义的检索策略,以识别所有符合条件的研究,评估这些研究的质量,并总结和分析研究结果。然后,根据NACI基于证据的流程,工作组提出建议并确定支持这些建议的证据等级。根据这些证据,NACI对这些建议进行审议并批准。
目前在加拿大获批使用的两种B群脑膜炎球菌疫苗不可互换,因为它们含有不同的抗原,且尚无关于将这两种产品联合接种系列疫苗产生的免疫原性的已发表研究。在对证据进行审查后,NACI建议,在应提供B群脑膜炎球菌疫苗的情况下,MenB-fHBP疫苗可被视为10岁及以上人群的一种选择:1)在B群脑膜炎球菌病暴发期间或出现预计对该疫苗敏感的高流行菌株时;2)对于与B群引起的侵袭性脑膜炎球菌病病例密切接触的个体;3)对于有基础疾病且使其患脑膜炎球菌病风险高于一般人群的个体;或4)对于接触B群脑膜炎球菌分离株风险高于一般人群的个体。NACI还建议,对于脑膜炎球菌病风险并不高于一般人群,但希望降低侵袭性B群脑膜炎球菌病风险的10至25岁个体,MenB-fHBP疫苗可被视为一种选择。
NACI建议,对于因基础疾病或接触风险增加而疾病风险较高的所有个体,接种B群IMD疫苗。除了为公共卫生决策者(即负责为公共资助的免疫计划做出决策的省份/地区)提供指导外,这些NACI建议还向个人、疫苗提供者和组织提供了关于可能目前未纳入公共资助免疫计划的疫苗的信息。NACI目前继续建议在加拿大的常规普遍免疫计划中不使用B群疫苗。