Mensah Anna A, Campbell Helen, Clark Stephen A, Ribeiro Sonia, Lucidarme Jay, Bai Xilian, Borrow Ray, Ladhani Shamez N
Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency, London, UK.
Meningococcal Reference Unit, UK Health Security Agency, Manchester, UK.
Lancet Child Adolesc Health. 2023 Mar;7(3):190-198. doi: 10.1016/S2352-4642(22)00379-0. Epub 2023 Jan 31.
In 2015, the UK included 4CMenB, a multi-component, recombinant protein-based vaccine against meningococcal serogroup B (MenB) disease, in the national infant immunisation programme. We aimed to assess the effect of 4CMenB vaccination on the severity of MenB disease presentation and outcomes.
In this active, prospective, national surveillance study, we used data from the UK Health Security Agency national surveillance of meningococcal disease. We included data from follow-up of children younger than 5 years with laboratory-confirmed MenB disease who were eligible for 4CMenB vaccination with general practice 3-6 months after disease onset. All invasive MenB isolates were tested using the Meningococcal Antigen Typing System to determine whether the isolate was potentially preventable by 4CMenB. Admission to intensive care, death, and, when possible, reported sequelae in survivors were reviewed alongside vaccine status. For the epidemiological analysis, we compared laboratory-confirmed MenB disease cases before 4CMenB implementation (Sept 1, 2010, to March 31, 2015) with those after implementation (Sept 1, 2015, to March 31, 2020). For clinical follow-up and outcomes, we included all children younger than 5 years with laboratory-confirmed MenB disease between Sept 1, 2015, and March 31, 2021.
Between Sept 1, 2015, and March 31, 2021, there were 371 cases of MenB disease in children younger than 5 years, including 256 (69%) in those younger than 1 year and 128 (35%) in those younger than 3 months. After the introduction of 4CMenB, the peak age of patients with MenB disease shifted from 5-6 months to 1-3 months. Overall, 108 (29%) of 371 children were too young for vaccination, unvaccinated, or developed MenB disease within 14 days of the first dose. Of 110 meningococcal strains characterised, 11 (92%) of 12 were potentially preventable by 4CMenB in unvaccinated children compared with 53 (66%) of 80 in partly vaccinated and 11 (69%) of 16 in fully vaccinated children. 78 (21%) of 371 children required intensive care, and the case fatality ratio was 5% (17 of 371), with 11 of 17 deaths occurring before 1 year of age, including seven in infants who were too young (<8 weeks) for vaccination. Of 354 survivors, 57 (16%) had 74 sequelae reported; 45 (61%) of 74 were neurological, 17 (23%) were physical, two (3%) were behavioural or psychological, and ten (14%) were other complications. Prevalence of sequelae was similar in unvaccinated (15 [15%] of 98) and vaccinated (42 [16%] 256) children, as were composite outcomes of death or sequelae, and intensive care or death or sequelae.
Cases of MenB disease in vaccine-eligible children declined after 4CMenB implementation, but morbidity in vaccinated and unvaccinated children remained unchanged, highlighting the importance of vaccination to prevent MenB disease. The lower peak age of infants with MenB disease after 4CMenB implementation, with a higher case fatality ratio in young infants, highlights the importance of timely vaccination.
UK Health Security Agency.
2015年,英国将4CMenB(一种针对B群脑膜炎球菌病的多组分重组蛋白疫苗)纳入国家婴儿免疫规划。我们旨在评估4CMenB疫苗接种对B群脑膜炎球菌病发病严重程度及转归的影响。
在这项前瞻性全国主动监测研究中,我们使用了英国卫生安全局对脑膜炎球菌病进行全国监测的数据。我们纳入了年龄小于5岁、实验室确诊为B群脑膜炎球菌病且在发病后3 - 6个月符合4CMenB疫苗接种条件的儿童随访数据。所有侵袭性B群脑膜炎球菌分离株均使用脑膜炎球菌抗原分型系统进行检测,以确定该分离株是否可被4CMenB预防。同时回顾了重症监护病房收治情况、死亡情况以及幸存者中可能报告的后遗症,并结合疫苗接种状态进行分析。在流行病学分析中,我们比较了4CMenB实施前(2010年9月1日至2015年3月31日)和实施后(2015年9月1日至2020年3月31日)实验室确诊的B群脑膜炎球菌病病例。对于临床随访及转归情况,我们纳入了2015年9月1日至2021年3月31日期间年龄小于5岁、实验室确诊为B群脑膜炎球菌病的所有儿童。
在2015年9月1日至2021年3月31日期间,年龄小于5岁的儿童中有371例B群脑膜炎球菌病病例,其中1岁以下儿童256例(69%),3个月以下儿童128例(35%)。引入4CMenB后,B群脑膜炎球菌病患者的发病高峰年龄从5 - 6个月转移至1 - 3个月。总体而言,371名儿童中有108名(29%)年龄太小无法接种疫苗、未接种疫苗或在首剂接种后14天内患上B群脑膜炎球菌病。在110株已鉴定的脑膜炎球菌菌株中,未接种疫苗儿童中的12株中有11株(92%)可能被4CMenB预防,部分接种疫苗儿童中的80株中有53株(66%),完全接种疫苗儿童中的16株中有11株(69%)。371名儿童中有78名(21%)需要重症监护,病死率为5%(371例中有17例),17例死亡中有11例发生在1岁之前,其中7例是年龄太小(<8周)无法接种疫苗的婴儿。在354名幸存者中,有57名(16%)报告有74种后遗症;74种后遗症中有45种(61%)是神经系统方面的,17种(23%)是身体方面的,2种(3%)是行为或心理方面的,10种(14%)是其他并发症。未接种疫苗儿童(98名中的15名[15%])和接种疫苗儿童(256名中的42名[16%])的后遗症患病率相似,死亡或后遗症的综合转归以及重症监护或死亡或后遗症的情况也相似。
4CMenB实施后,符合疫苗接种条件儿童中的B群脑膜炎球菌病病例有所减少,但接种疫苗和未接种疫苗儿童的发病率保持不变,这凸显了疫苗接种对预防B群脑膜炎球菌病的重要性。4CMenB实施后,B群脑膜炎球菌病婴儿的发病高峰年龄降低,且小婴儿的病死率较高,这凸显了及时接种疫苗的重要性。
英国卫生安全局。