COVID-19 大流行前后脑膜炎球菌致病血清群的全球流行病学:叙述性回顾。

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES Infectious Diseases and Therapy Pub Date : 2024-12-01 Epub Date: 2024-11-07 DOI:10.1007/s40121-024-01063-5
Steven Shen, Jamie Findlow, Paula Peyrani
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引用次数: 0

摘要

侵袭性脑膜炎球菌病(IMD)与高发病率和高死亡率有关,主要由五种奈瑟氏脑膜炎球菌血清群(A/B/C/W/Y)引起。多糖结合疫苗可诱导 T 细胞依赖性免疫反应,在婴儿和成人中具有免疫原性,并可减少带菌率,对高带菌率年龄组接种疫苗可为未接种者提供间接保护(群体免疫)。成功的疫苗接种计划必须适合当地的流行病学,流行病学因地域、时间、年龄和血清群而异。血清 A 组 IMD 曾经在全球占主导地位,但在大规模疫苗接种计划后已基本消失。从 2010 年到 2018 年,B 血清群是全球许多地区 IMD 的主要病因,通常影响较年轻的年龄组。20 世纪 90 年代,血清 C 群克隆复合体-11 IMD 的传播促使许多国家实施了 MenC 疫苗接种计划,导致流行率下降。到 2010 年代中期,C 血清群仍占全球 IMD 的 20%以上。2000 年朝觐疫情暴发后,血清 W 群成为全球 IMD 的重要致病因素;随后,许多地区报告的地方病和疫情暴发在流行前有所增加。血清 Y 群于 20 世纪 90 年代出现,成为各地区 IMD 的重要病因,2010 年至 2018 年期间流行率有所上升或趋于稳定。血清 X 群在非洲脑膜炎带之外并不常见,其流行率在 COVID-19 大流行之前就已下降。在大流行期间,全球 IMD 下降,随后一般由大流行前流行且主要影响未接种疫苗的年龄组(尤其是青少年/年轻成人)的血清群引起重新流行。最近的 IMD 流行病学强调了为高危年龄组接种区域流行血清群疫苗的重要性;例如,最近通过资格预审的 MenACWXY 疫苗中的抗 X 血清群成分在非洲脑膜炎带以外地区可能只能提供有限的保护。在其他地区,接种针对 MenB 和 MenACWY 的综合疫苗似乎更为合适,最近批准的 MenABCWY 疫苗可以简化接种程序。
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Global Epidemiology of Meningococcal Disease-Causing Serogroups Before and After the COVID-19 Pandemic: A Narrative Review.

Invasive meningococcal disease (IMD) is associated with high morbidity and mortality and predominantly caused by five Neisseria meningitidis serogroups (A/B/C/W/Y). Polysaccharide conjugate vaccines induce T-cell-dependent immune responses, are immunogenic in infants and adults, and reduce carriage, and vaccination of age groups associated with high-carriage can provide indirect protection in the unvaccinated (herd immunity). Successful vaccination programs must be tailored to local epidemiology, which varies geographically, temporally, and by age and serogroup. Serogroup A IMD once predominated globally, but has largely disappeared following mass vaccination programs. Serogroup B was a predominant cause of IMD in many global regions from 2010 to 2018, typically affecting younger age groups. Spread of serogroup C clonal complex-11 IMD in the 1990s prompted implementation of MenC vaccine programs in many countries, resulting in declines in prevalence. Serogroup C still caused > 20% of global IMD through the mid-2010s. Serogroup W became a significant contributor to global IMD after Hajj pilgrimage outbreaks in 2000; subsequent increases of endemic disease and outbreaks were reported pre-pandemic in many regions. Serogroup Y emerged in the 1990s as a significant cause of IMD throughout various regions and prevalence had increased or stabilized from 2010 to 2018. Serogroup X is uncommon outside the African meningitis belt, and its prevalence has declined since before the COVID-19 pandemic. Global IMD declines during the pandemic were followed by resurgences generally caused by serogroups that were prevalent pre-pandemic and affecting mainly unvaccinated age groups (particularly adolescents/young adults). Recent IMD epidemiology underscores the importance of vaccinating at-risk age groups against regionally prevalent serogroups; for example, the anti-serogroup X component of the recently prequalified MenACWXY vaccine is likely to provide limited protection outside the African meningitis belt. In other regions, comprehensive vaccination against MenB and MenACWY, which could be streamlined by the recently approved MenABCWY vaccine, seems more appropriate.

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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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