Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Department of Biology, Emory University, Atlanta, Georgia, USA.
Clin Infect Dis. 2023 Feb 8;76(3):479-486. doi: 10.1093/cid/ciac725.
Developing accurate and reliable methods to estimate vaccine protection is a key goal in immunology and public health. While several statistical methods have been proposed, their potential inaccuracy in capturing fast intraseasonal waning of vaccine-induced protection needs to be rigorously investigated.
To compare statistical methods for estimating vaccine effectiveness (VE), we generated simulated data using a multiscale, agent-based model of an epidemic with an acute viral infection and differing extents of VE waning. We apply a previously proposed framework for VE measures based on the observational data richness to assess changes of vaccine-induced protection over time.
While VE measures based on hard-to-collect information (eg, the exact timing of exposures) were accurate, usually VE studies rely on time-to-infection data and the Cox proportional hazards model. We found that its extension using scaled Schoenfeld residuals, previously proposed for capturing VE waning, was unreliable in capturing both the degree of waning and its functional form and identified the mathematical factors contributing to this unreliability. We showed that partitioning time and including a time-vaccine interaction term in the Cox model significantly improved estimation of VE waning, even in the case of dramatic, rapid waning. We also proposed how to optimize the partitioning scheme.
While appropriate for rejecting the null hypothesis of no waning, scaled Schoenfeld residuals are unreliable for estimating the degree of waning. We propose a Cox-model-based method with a time-vaccine interaction term and further optimization of partitioning time. These findings may guide future analysis of VE waning data.
开发准确可靠的方法来估计疫苗保护效果是免疫学和公共卫生的一个关键目标。虽然已经提出了几种统计方法,但它们在捕捉疫苗诱导保护的快速季节性衰减方面可能存在不准确,需要进行严格的研究。
为了比较估计疫苗效力(VE)的统计方法,我们使用具有急性病毒感染和不同 VE 衰减程度的多尺度、基于代理的传染病模型生成模拟数据。我们应用了一种以前提出的基于观测数据丰富度的 VE 度量框架,以评估随时间变化的疫苗诱导保护的变化。
虽然基于难以收集的信息(例如,暴露的确切时间)的 VE 度量是准确的,但通常 VE 研究依赖于感染时间数据和 Cox 比例风险模型。我们发现,使用扩展后的比例 Schoenfeld 残差来捕捉 VE 衰减的方法不可靠,无法准确捕捉衰减的程度和其功能形式,并确定了导致这种不可靠性的数学因素。我们表明,在 Cox 模型中划分时间并包含时间-疫苗相互作用项,可以显著提高 VE 衰减的估计,即使在急剧快速衰减的情况下也是如此。我们还提出了如何优化分区方案。
虽然适用于拒绝无衰减的零假设,但比例 Schoenfeld 残差不可靠,无法估计衰减的程度。我们提出了一种基于 Cox 模型的方法,其中包含时间-疫苗相互作用项,并进一步优化了时间分区。这些发现可能为未来的 VE 衰减数据分析提供指导。