Immunisation and Countermeasures Division, Public Health England, Colindale, London NW9 5EQ, UK; Paediatric Infectious Diseases Research Group (PIDRG), St. George's University of London, Cranmer Terrace, London SW17 0RE, UK.
Immunisation and Countermeasures Division, Public Health England, Colindale, London NW9 5EQ, UK.
Vaccine. 2022 Mar 1;40(10):1493-1498. doi: 10.1016/j.vaccine.2021.12.010. Epub 2022 Feb 8.
Timely vaccination is critical for providing early protection against meningococcal B (MenB) disease because of the high incidence in early childhood. We assessed the timeliness of vaccination in children with confirmed MenB disease after 4CMenB (a recombinant protein-based vaccine) implementation into the national infant immunisation programme in England.
Public Health England (PHE) conducts surveillance of invasive meningococcal disease (IMD) in England. Children born since 01 July 2015 who developed MenB disease between 01 September 2015 and 31 August 2019 (four surveillance years) were included in the analysis.
There were 276 children with laboratory-confirmed MenB disease, including 36 infants who were too young for vaccination, 59 who were eligible for one 4CMenB dose, 104 for two doses and 77 for 3 doses before they developed MenB disease. Prior to developing MenB disease, there were 59 opportunities for vaccination with two 4CMenB doses in 48/104 (46.5%) eligible infants and 41 opportunities in 28/77 (36.6%) children aged ≥ 1 year who were under-immunised. A schedule with a shorter interval at 8 and 12 weeks of age, compared to the current schedule at 8 and 16 weeks, had the potential to offer an additional 4CMenB dose to 35/58 infants (58.6%) who developed MenB disease between 10 and 18 weeks of age.
A high proportion of infants and toddlers with laboratory-confirmed MenB disease had not received their scheduled 4CMenB vaccine prior to developing MenB disease. An infant priming schedule with a shorter interval of 4 weeks has the potential to provide earlier protection against MenB disease.
由于婴幼儿期脑膜炎奈瑟菌 B 型(MenB)病的发病率较高,及时接种疫苗对于提供早期保护至关重要。我们评估了英格兰国家婴儿免疫计划实施 4CMenB(一种基于重组蛋白的疫苗)后确诊为 MenB 病的儿童的疫苗接种及时性。
英国公共卫生署(PHE)对英格兰侵袭性脑膜炎球菌病(IMD)进行监测。2015 年 7 月 1 日以后出生、2015 年 9 月 1 日至 2019 年 8 月 31 日(4 个监测年)期间确诊为 MenB 病的儿童纳入分析。
共有 276 例实验室确诊的 MenB 病患儿,其中 36 例患儿年龄太小无法接种疫苗,59 例患儿有资格接种 1 剂 4CMenB,104 例患儿有资格接种 2 剂,77 例患儿有资格接种 3 剂,但在发病前已错过接种 2 剂 4CMenB 的机会。在发病前,48/104(46.5%)符合条件的婴儿有 59 次接种 2 剂 4CMenB 的机会,28/77(36.6%)未免疫的 1 岁以上儿童有 41 次机会。与目前 8 周和 16 周的间隔相比,8 周和 12 周的间隔较短的方案有可能为 10 至 18 周发病的 35/58(58.6%)婴儿提供额外的 4CMenB 剂量。
实验室确诊的 MenB 病婴幼儿中有很大一部分在发病前未接种规定的 4CMenB 疫苗。间隔 4 周的婴儿初免方案有可能更早地提供针对 MenB 病的保护。