An immunity-driven modelling framework for epidemics of non-sterilizing infections.

IF 3.4 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Daniel Stocks, Amy Thomas, Ellen Brooks-Pollock, Leon Danon
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Abstract

Protecting populations against pathogens that induce non-sterilizing immunity remains a major public health challenge. However, conventional mathematical models are often incompatible with within-host data, offering limited insight into how immune responses drive epidemics. To address this gap, we develop a modular, data-driven mathematical framework that links immunological and virological dynamics to population-level transmission. Our approach derives infectiousness from viral load and protection against reinfection from time-varying immune responses, allowing epidemic trajectories to emerge from the summation of individual-level processes. As an example, we use viral load quantified in a SARS-CoV-2 human challenge study and binding antibody levels post-vaccination against SARS-CoV-2. The framework captures individual-level infection dynamics and shows that immune responses fundamentally shape epidemic trajectories. We show that weak correlations between antibody levels and protection lead to frequent reinfections and endemic circulation, whereas strong correlations generate recurrent explosive outbreaks. We fit the model to simulated case data to demonstrate its ability to recover underlying protection and reinfection dynamics. Applied to real-world data, this framework could provide new insights into the drivers of epidemic patterns and inform vaccination strategies for pathogens with non-sterilizing immunity.

非消毒感染流行的免疫驱动模型框架。
保护人群免受引起非灭菌性免疫的病原体的侵害仍然是一项重大的公共卫生挑战。然而,传统的数学模型往往与宿主内的数据不兼容,对免疫反应如何驱动流行病提供了有限的见解。为了解决这一差距,我们开发了一个模块化的、数据驱动的数学框架,将免疫学和病毒学动力学与人群水平的传播联系起来。我们的方法从病毒载量中获得传染性,从时变免疫反应中获得对再感染的保护,允许从个体水平过程的总和中产生流行轨迹。例如,我们使用了SARS-CoV-2人类挑战研究中量化的病毒载量和接种SARS-CoV-2疫苗后的结合抗体水平。该框架捕获了个体层面的感染动态,并表明免疫反应从根本上塑造了流行病的轨迹。我们表明,抗体水平和保护之间的弱相关性导致频繁的再感染和地方性流行,而强相关性导致反复爆发。我们将模型拟合到模拟病例数据中,以证明其恢复潜在保护和再感染动态的能力。将该框架应用于现实世界的数据,可以为流行模式的驱动因素提供新的见解,并为具有非灭菌免疫的病原体的疫苗接种策略提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of The Royal Society Interface
Journal of The Royal Society Interface 综合性期刊-综合性期刊
CiteScore
7.10
自引率
2.60%
发文量
234
审稿时长
2.5 months
期刊介绍: J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.
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