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Role of factor H binding protein in Neisseria meningitidis virulence and its potential as a vaccine candidate to broadly protect against meningococcal disease.因子 H 结合蛋白在脑膜炎奈瑟菌毒力中的作用及其作为广泛预防脑膜炎球菌病疫苗候选物的潜力。
Microbiol Mol Biol Rev. 2013 Jun;77(2):234-52. doi: 10.1128/MMBR.00056-12.
2
Controlling serogroup B invasive meningococcal disease: the Canadian perspective.控制 B 群侵袭性脑膜炎球菌病:加拿大的观点。
Expert Rev Vaccines. 2013 May;12(5):505-17. doi: 10.1586/erv.13.30.
3
Diversity of Canadian meningococcal serogroup B isolates and estimated coverage by an investigational meningococcal serogroup B vaccine (4CMenB).加拿大脑膜炎奈瑟菌 B 群分离株的多样性和一种脑膜炎奈瑟菌 B 群候选疫苗(4CMenB)的估计保护率。
Vaccine. 2013 Dec 17;32(1):124-30. doi: 10.1016/j.vaccine.2013.03.063. Epub 2013 Apr 12.
4
Introducing vaccination against serogroup B meningococcal disease: an economic and mathematical modelling study of potential impact.引入 B 群脑膜炎奈瑟菌疾病疫苗接种:潜在影响的经济和数学建模研究。
Vaccine. 2013 May 28;31(23):2638-46. doi: 10.1016/j.vaccine.2013.03.034. Epub 2013 Apr 6.
5
[Characterization of Neisseria meningitidis strains isolated from carriers in Cuba during 20 years].[古巴20年间从携带者中分离出的脑膜炎奈瑟菌菌株的特征分析]
Rev Cubana Med Trop. 2006 May-Aug;58(2):124-33.
6
Predicted strain coverage of a meningococcal multicomponent vaccine (4CMenB) in Europe: a qualitative and quantitative assessment.预测脑膜炎球菌多组份疫苗(4CMenB)在欧洲的菌株覆盖率:定性和定量评估。
Lancet Infect Dis. 2013 May;13(5):416-25. doi: 10.1016/S1473-3099(13)70006-9. Epub 2013 Feb 13.
7
Cost-effectiveness of vaccination against meningococcal B among Dutch infants: Crucial impact of changes in incidence.接种 B 型脑膜炎球菌疫苗在荷兰婴儿中的成本效益:发病率变化的关键影响。
Hum Vaccin Immunother. 2013 May;9(5):1129-38. doi: 10.4161/hv.23888. Epub 2013 Feb 13.
8
Cysteine depletion causes oxidative stress and triggers outer membrane vesicle release by Neisseria meningitidis; implications for vaccine development.半胱氨酸耗竭导致氧化应激,并触发脑膜炎奈瑟菌的外膜囊泡释放;对疫苗开发的影响。
PLoS One. 2013;8(1):e54314. doi: 10.1371/journal.pone.0054314. Epub 2013 Jan 23.
9
Immunogenicity and safety of an investigational multicomponent, recombinant, meningococcal serogroup B vaccine (4CMenB) administered concomitantly with routine infant and child vaccinations: results of two randomised trials.同时接种研究性多种成分、重组、脑膜炎奈瑟菌 B 型疫苗(4CMenB)与常规婴儿和儿童疫苗的免疫原性和安全性:两项随机试验结果。
Lancet. 2013 Mar 9;381(9869):825-35. doi: 10.1016/S0140-6736(12)61961-8.
10
Preclinical safety and immunogenicity evaluation of a nonavalent PorA native outer membrane vesicle vaccine against serogroup B meningococcal disease.九价荚膜多糖原代外膜囊疫苗预防 B 群脑膜炎球菌病的临床前安全性和免疫原性评价。
Vaccine. 2013 Feb 4;31(7):1065-71. doi: 10.1016/j.vaccine.2012.12.031. Epub 2012 Dec 27.

新型与旧型B群脑膜炎球菌疫苗:新型疫苗如何使婴幼儿受益。

New versus old meningococcal group B vaccines: how the new ones may benefit infants & toddlers.

作者信息

Panatto D, Amicizia D, Lai P L, Cristina M L, Domnich A, Gasparini R

机构信息

Department of Health Sciences, University of Genoa, Genoa, Italy.

出版信息

Indian J Med Res. 2013 Dec;138(6):835-46.

PMID:24521624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3978970/
Abstract

Invasive disease caused by Neisseria meningitidis is associated with high mortality and high disability rates and mainly affects children under one year of age. Vaccination is the best way to prevent meningococcal disease, especially in infants and toddlers. The introduction of massive meningococcal serogroup C vaccination has drastically reduced the incidence of disease caused by this serogroup, and serogroup B has now become the main causative agent in several industrialized countries. The first serogroup B vaccines, which were used for more than two decades, were based on outer membrane vesicles and proved to be protective only against specific epidemic strains in Cuba, Norway, Brazil and New Zealand. Moreover, these often elicited a scant immune response in young children. Innovative genomics-based reverse vaccinology subsequently enabled researchers to identify genes encoding for surface proteins that are able to elicit a strong immune response against several B strains. This important discovery led to the development and recent approval in Europe of the four-component meningococcal serogroup B (4CMenB) vaccine. Large clinical trials have shown high immunogenicity and tolerability and acceptable safety levels of 4CMenB in infants and toddlers. This vaccine is expected to cover a large number of circulating invasive strains and may also be efficacious against other serogroups. Young children are particularly vulnerable to the devastating consequences of meningococcal disease. Given the high performance of 4CMenB and its non-interference with routine vaccinations, this age-group will be the first to benefit from the introduction of this vaccine.

摘要

脑膜炎奈瑟菌引起的侵袭性疾病与高死亡率和高致残率相关,主要影响一岁以下儿童。接种疫苗是预防脑膜炎球菌病的最佳方法,尤其是对婴幼儿。大规模接种C群脑膜炎球菌疫苗已大幅降低了该血清群所致疾病的发病率,而B群脑膜炎球菌目前已成为多个工业化国家的主要病原体。最初使用了二十多年的B群脑膜炎球菌疫苗是基于外膜囊泡,结果证明仅对古巴、挪威、巴西和新西兰的特定流行菌株具有保护作用。此外,这些疫苗在幼儿中往往引发微弱的免疫反应。基于创新基因组学的反向疫苗学随后使研究人员能够识别编码表面蛋白的基因,这些表面蛋白能够引发针对多种B群菌株的强烈免疫反应。这一重要发现促成了四价B群脑膜炎球菌结合疫苗(4CMenB)的研发及其近期在欧洲获批。大型临床试验表明,4CMenB在婴幼儿中具有高免疫原性和耐受性,且安全性水平可接受。这种疫苗有望覆盖大量流行的侵袭性菌株,也可能对其他血清群有效。幼儿特别容易受到脑膜炎球菌病毁灭性后果的影响。鉴于4CMenB的卓越性能及其对常规疫苗接种无干扰,这一年龄组将首先受益于该疫苗的引入。