Institute of Child Health and Human Development, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.
Department of Virology, Research Institute for Tropical Medicine, Muntinlupa, Philippines.
Lancet Infect Dis. 2024 Jul;24(7):737-745. doi: 10.1016/S1473-3099(24)00099-9. Epub 2024 Mar 22.
A three-dose dengue vaccine (CYD-TDV) was licensed for use in children aged 9 years and older starting in 2015 in several dengue-endemic countries. In 2016, the Philippine Department of Health implemented a dengue vaccination programme, which was discontinued because of safety concerns. We assessed the relative risk of developing virologically confirmed dengue among children who did or did not receive a single dose of CYD-TDV by previous dengue virus (DENV) infections at baseline classified as none, one, and two or more infections.
In this longitudinal, prospective, population-based cohort study, we enrolled healthy children (aged 9-14 years) residing in Bogo or Balamban, Cebu, Philippines, between May 2, and June 2, 2017, before a mass dengue vaccination campaign, via the Rural Health Unit in Bogo and three Rural Health Units in Balamban. We collected demographic information and sera for baseline DENV serostatus and conducted active surveillance for acute febrile illness. Children who developed acute febrile illness were identified, clinical data were collected, and blood was drawn for confirmation of dengue by RT-PCR. The primary outcome was the relative risk of developing virologically confirmed dengue among children who received or did not receive a single dose of CYD-TDV by DENV serostatus at baseline.
A single dose of CYD-TDV did not confer protection against virologically confirmed dengue in children who had none or one previous DENV infection at baseline. One dose conferred significant protection against hospital admission for virologically confirmed dengue among participants who had two or more previous DENV infections at baseline during the first 3 years (70%, 95% CI 20-88; p=0·017) and the entire follow-up period (67%, 19-87; p=0·016).
The risk of developing virologically confirmed dengue after a single dose of CYD-TDV varied by baseline DENV serostatus. Since the study assessed the effect of only a single dose, the findings cannot inform decisions on vaccination by public health officers. However, the findings have implications for children who receive an incomplete vaccination regimen and these results should prompt more detailed analyses in future trials on dengue vaccines.
The Philippine Department of Health, Hanako Foundation, WHO, Swedish International Development Cooperation Agency, International Vaccine Institute, University of North Carolina, and US National Institute of Allergy and Infectious Diseases.
自 2015 年以来,几种登革热流行国家已批准将三剂登革热疫苗(CYD-TDV)用于 9 岁及以上儿童。2016 年,菲律宾卫生部实施了登革热疫苗接种计划,但因安全性问题而停止。我们评估了基线时既往登革热病毒(DENV)感染无、1 次和 2 次或更多次感染的儿童中,单次接受或未接受 CYD-TDV 疫苗接种的儿童中,经病毒学证实的登革热的相对风险。
在这项纵向、前瞻性、基于人群的队列研究中,我们于 2017 年 5 月 2 日至 6 月 2 日在菲律宾宿务的 Bogo 或 Balamban 通过 Bogo 的农村卫生单位和 Balamban 的三个农村卫生单位招募了健康儿童(9-14 岁),进行大规模登革热疫苗接种运动之前。我们收集了人口统计学信息和血清,用于检测基线 DENV 血清状态,并进行急性发热性疾病的主动监测。确定发生急性发热性疾病的儿童,收集临床数据,并通过 RT-PCR 抽取血液以确认登革热。主要结局是基线时 DENV 血清状态下接受或未接受单次 CYD-TDV 疫苗接种的儿童中,经病毒学证实的登革热的相对风险。
在基线时无或仅有 1 次既往 DENV 感染的儿童中,单次 CYD-TDV 疫苗接种不能预防经病毒学证实的登革热。在基线时有 2 次或更多既往 DENV 感染的参与者中,在第 1 个 3 年期间(70%,95%CI 20-88;p=0.017)和整个随访期间(67%,19-87;p=0.016),单次剂量可显著预防经病毒学证实的登革热住院。
接受单次 CYD-TDV 疫苗接种后,经病毒学证实的登革热的风险随基线 DENV 血清状态而异。由于该研究仅评估了单次剂量的效果,因此研究结果不能为公共卫生官员的疫苗接种决策提供信息。然而,研究结果对接受不完全疫苗接种方案的儿童具有影响,这些结果应促使在未来的登革热疫苗试验中进行更详细的分析。
菲律宾卫生部、Hanako 基金会、世卫组织、瑞典国际开发合作署、国际疫苗研究所、北卡罗来纳大学和美国国立过敏和传染病研究所。