Willemsen Joukje E, Borghans José A M, Bont Louis J, Drylewicz Julia
Centre for Translational Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Division of Infectious Diseases, Department of Pediatrics, University Medical Centre Utrecht, Utrecht, The Netherlands.
Vaccine X. 2023 Sep 1;15:100379. doi: 10.1016/j.jvacx.2023.100379. eCollection 2023 Dec.
Respiratory syncytial virus (RSV) is a leading cause of childhood mortality in infants below 6 months of age. In low-income and middle-income countries (LMICs), the public health burden is substantial and resources are limited. It is critical to inform decision makers about effectiveness of new interventions.
We developed a mathematical model where individual RSV subtype A (RSV-A) and B (RSV-B) maternally derived neutralizing titers were predicted at time of birth after maternal vaccination with the RSV prefusion F protein-based vaccine. We estimated the subsequent duration of vaccine-induced immunity and compared this to the age at time of death distribution in the RSV GOLD Mortality Database to predict the potential impact of maternal vaccination on RSV-related childhood mortality. We used country-specific timing of antenatal care visits distributions and mortality estimates to make country-specific predictions for number of cases averted.
The model predicts that on average a neonate born at 40 weeks gestational age will be protected between 6 and 7 months from RSV-A and approximately 5 months from RSV-B related mortality. We estimated the potential impact of RSV-related mortality for in-hospital and out-of-hospital cases in LMICs and predicted that in 51 GAVI-eligible countries maternal vaccination could avert between 55% and 63% of the RSV-related in-hospital mortality cases below 6 months of age.
We show that maternal vaccination could substantially decrease RSV-A and RSV-B related in-hospital and out-of-hospital mortality in LMICs in the first 6 months of life.
呼吸道合胞病毒(RSV)是6个月以下婴儿儿童死亡的主要原因。在低收入和中等收入国家(LMICs),公共卫生负担沉重且资源有限。让决策者了解新干预措施的有效性至关重要。
我们开发了一个数学模型,用于预测母亲接种基于RSV预融合F蛋白疫苗后出生时个体RSV A亚型(RSV-A)和B亚型(RSV-B)的母源中和滴度。我们估计了疫苗诱导免疫的后续持续时间,并将其与RSV全球死亡率数据库中的死亡年龄分布进行比较,以预测母亲接种疫苗对RSV相关儿童死亡率的潜在影响。我们使用特定国家的产前检查就诊时间分布和死亡率估计来对避免的病例数进行特定国家的预测。
该模型预测,平均而言,孕40周出生的新生儿将在6至7个月内受到RSV-A的保护,在约5个月内受到RSV-B相关死亡的保护。我们估计了LMICs中住院和院外病例中RSV相关死亡率的潜在影响,并预测在51个符合全球疫苗免疫联盟(GAVI)条件的国家,母亲接种疫苗可避免55%至63%的6个月以下婴儿RSV相关住院死亡病例。
我们表明,母亲接种疫苗可大幅降低LMICs中6个月以下婴儿RSV-A和RSV-B相关的住院和院外死亡率。