Division of Infectious Disease, Key Laboratory of Surveillance and Early-Warning on Infectious Disease, Chinese Center for Disease Control and Prevention, Beijing, China; WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
School of Public Health, Fudan University, Key Laboratory of Public Health Safety, Ministry of Education, Shanghai, China.
Lancet Child Adolesc Health. 2019 Oct;3(10):697-704. doi: 10.1016/S2352-4642(19)30185-3. Epub 2019 Jul 30.
Inactivated monovalent enterovirus A71 (EV-A71) vaccines are now available in China to reduce the substantial public health burden of hand, foot, and mouth disease. However, post-licensure monitoring of vaccine effectiveness is important. We did an observational test-negative study of EV-A71 vaccine effectiveness.
Children with hand, foot, and mouth disease who were admitted to Henan Children's Hospital (Zhengzhou, China) within 7 days of illness onset were invited to participate in this test-negative case-control study. Participant vaccination history with EV-A71, including the number of doses received and the date of each dose of vaccination, was elicited from parents or legal guardians of participants with a standardised questionnaire. Children must have received two doses before hospitalisation to be counted as fully vaccinated. Patients who had received a single dose before hospitalisation were classified as partly vaccinated. Children who had received no EV-A71 vaccine before hospitalisation were classified as unvaccinated. Throat swabs and stool samples collected from patients were tested by RT-PCR to identify EV-A71 and other enteroviruses. The primary outcome of the study was paediatric hand, foot, and mouth disease associated with EV-A71 requiring hospitalisation. We estimated vaccine effectiveness with conditional logistic regression models adjusted for potential confounders.
Between Feb 15, 2017, and Feb 15, 2018, we enrolled 1803 children aged 6-71 months with hand, foot, and mouth disease. 234 (13%) children tested positive for EV-A71, 1529 (85%) tested positive for other enteroviruses-528 (29%) were positive for Coxsackievirus (CV)-A6 and 342 (19%) were positive for CV-A16-and 29 (2%) tested negative for all enteroviruses. 11 (1%) children with neither throat swab nor stool testing results were excluded from further analyses. Overall vaccine effectiveness was estimated to be 85·4% (95% CI 53·2 to 95·4) for fully vaccinated children and 63·1% (13·1 to 84·3) for partly vaccinated children. The vaccine effectiveness for full vaccination was estimated to be 91·1% (35·1 to 98·8) among non-severe cases compared with 73·3% (-32·6 to 94·6) in severe cases. The vaccine effectiveness for partial vaccination was 77·9% (4·3 to 94·9) in children aged 24-71 months and 40·8% (-71·1 to 79·5) in children aged 6-23 months. We found no significant association between full or partial vaccination and CV-A6 or CV-A16-related hand, foot, and mouth disease.
EV-A71 vaccination was effective in preventing non-severe hand, foot, and mouth disease associated with EV-A71 virus infection in children aged 6-71 months, and we found evidence that one dose of vaccination provided partial protection for children aged 24-71 months. Introduction of multivalent vaccines could further reduce the burden of hand, foot, and mouth disease.
The National Science Fund for Distinguished Young Scholars.
中国现已提供灭活单价肠道病毒 A71(EV-A71)疫苗,以减轻手足口病造成的巨大公共卫生负担。然而,疫苗上市后效果的监测非常重要。我们开展了一项 EV-A71 疫苗效果的观察性病例对照研究。
发病后 7 天内入住河南儿童医院(郑州,中国)的手足口病患儿受邀参加这项无病例对照研究。通过标准化问卷从患儿的父母或法定监护人处获取 EV-A71 疫苗接种史,包括接种的剂次和每剂接种的日期。患儿必须在住院前接种 2 剂才被视为完全接种。在住院前接种 1 剂的患儿被归类为部分接种。在住院前未接种过 EV-A71 疫苗的患儿被归类为未接种。从患者采集的咽拭子和粪便样本通过 RT-PCR 检测 EV-A71 和其他肠道病毒。研究的主要结局是需要住院治疗的由 EV-A71 引起的儿科手足口病。我们使用条件逻辑回归模型估计了疫苗的有效性,并对潜在的混杂因素进行了调整。
在 2017 年 2 月 15 日至 2018 年 2 月 15 日期间,我们纳入了 1803 名年龄在 6-71 个月的手足口病患儿。234 名(13%)患儿的肠道病毒检测呈阳性,1529 名(85%)患儿的其他肠道病毒检测呈阳性-528 名(29%)为柯萨奇病毒(CV)-A6 阳性,342 名(19%)为 CV-A16 阳性,29 名(2%)患儿所有肠道病毒检测均呈阴性。29 名(2%)未进行咽拭子或粪便检测的患儿被排除在进一步分析之外。总体而言,完全接种疫苗的患儿疫苗有效性估计为 85.4%(95%CI,53.2-95.4),部分接种疫苗的患儿为 63.1%(13.1-84.3)。非重症病例中,全接种疫苗的疫苗有效性估计为 91.1%(35.1-98.8),重症病例中为 73.3%(-32.6-94.6)。部分接种疫苗在 24-71 月龄儿童中的疫苗有效性为 77.9%(4.3-94.9),在 6-23 月龄儿童中的疫苗有效性为 40.8%(-71.1-79.5)。我们未发现全或部分接种与 CV-A6 或 CV-A16 相关的手足口病之间存在显著关联。
EV-A71 疫苗在预防 6-71 月龄儿童中由 EV-A71 病毒感染引起的非重症手足口病方面是有效的,我们有证据表明,1 剂疫苗接种可为 24-71 月龄儿童提供部分保护。引入多价疫苗可以进一步减轻手足口病的负担。
国家杰出青年科学基金。