Meningococcal Reference Unit, Public Health England, Floor 2 Clinical Sciences Building 2, Manchester Royal Infirmary, Manchester, M13 9WL, United Kingdom.
Meningococcal Reference Unit, Public Health England, Floor 2 Clinical Sciences Building 2, Manchester Royal Infirmary, Manchester, M13 9WL, United Kingdom.
J Infect. 2022 Feb;84(2):136-144. doi: 10.1016/j.jinf.2021.11.015. Epub 2021 Nov 25.
In 2015 the UK became the first country to implement the meningococcal B (MenB) vaccine, 4CMenB, into the national infant program. 4CMenB is expected to cover meningococci expressing sufficient levels of cross-reactive proteins. This study presents clonal complex, 4CMenB antigen genotyping, and 4CMenB coverage data for all English invasive MenB isolates from 2014/15 (1 year pre-vaccine) through 2017/18 and compares data from vaccinated and unvaccinated ≤3 year olds.
Vaccine coverage of all invasive MenB isolates from 2014/15 to 2017/18 (n = 784) was analysed using the Meningococcal Antigen Typing System. Genotyping utilised the Meningococcus Genome Library.
Among ≤3 year olds, proportionally fewer cases in vaccinees (1, 2 or 3 doses) were associated with well-covered strains e.g. cc41/44 (20.5% versus 36.4%; P<0.01) and antigens e.g. PorA P1.4 (7.2% versus 17.3%; P = 0.02) or fHbp variant 1 peptides (44.6% vs 69.1%; P<0.01). Conversely, proportionally more cases in vaccinees were associated with poorly-covered strains e.g. cc213 (22.9% versus 9.6%; P<0.01) and antigens e.g. variant 2 or 3 fHbp peptides (54.2% versus 30.9%; P<0.01).
4CMenB reduces disease due to strains with cross-reactive antigen variants. No increase in absolute numbers of cases due to poorly covered strains was observed in the study period.
2015 年,英国成为首个将脑膜炎 B 型(MenB)疫苗 4CMenB 纳入国家婴儿计划的国家。4CMenB 有望覆盖表达足够交叉反应蛋白的脑膜炎奈瑟菌。本研究介绍了 2014/15 年(疫苗接种前一年)至 2017/18 年期间所有英国侵袭性 MenB 分离株的克隆复合体、4CMenB 抗原基因分型和 4CMenB 覆盖率数据,并比较了接种疫苗和未接种疫苗的≤3 岁儿童的数据。
使用脑膜炎球菌抗原分型系统分析了 2014/15 年至 2017/18 年期间所有侵袭性 MenB 分离株的疫苗覆盖率(n=784)。基因分型利用脑膜炎球菌基因组文库进行。
在≤3 岁的儿童中,接种疫苗的病例中比例较低的是具有良好覆盖的菌株,例如 cc41/44(20.5%对 36.4%;P<0.01)和抗原,例如 PorA P1.4(7.2%对 17.3%;P=0.02)或 fHbp 变体 1 肽(44.6%对 69.1%;P<0.01)。相反,接种疫苗的病例中比例较高的是覆盖较差的菌株,例如 cc213(22.9%对 9.6%;P<0.01)和抗原,例如变体 2 或 3 fHbp 肽(54.2%对 30.9%;P<0.01)。
4CMenB 减少了具有交叉反应抗原变体的菌株引起的疾病。在研究期间,未观察到具有较差覆盖能力的菌株的病例数量绝对增加。