Predicting immune protection against outcomes of infectious disease from population-level effectiveness data with application to COVID-19

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2025-03-20 DOI:10.1016/j.vaccine.2025.126987
Tianxiao Hao , Gerard E. Ryan , Michael J. Lydeamore , Deborah Cromer , James G. Wood , Jodie McVernon , James M. McCaw , Freya M. Shearer , Nick Golding
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Abstract

Quantifying the extent to which previous infections and vaccinations confer protection against future infection or disease outcomes is critical to managing the transmission and consequences of infectious diseases.
We present a general statistical model for predicting the strength of protection conferred by different immunising exposures (numbers, types, and strains of both vaccines and infections), against multiple outcomes of interest, whilst accounting for immune waning. We predict immune protection against key clinical outcomes: developing symptoms, hospitalisation, and death. We also predict transmission-related outcomes: acquisition of infection and onward transmission in breakthrough infections. These enable quantification of the impact of immunity on population-level transmission dynamics. Our model calibrates the level of immune protection, drawing on both population-level data, such as vaccine effectiveness estimates, and neutralising antibody levels as a correlate of protection. This enables the model to learn realised immunity levels beyond those which can be predicted by antibody kinetics or other correlates alone.
We demonstrate an application of the model for SARS-CoV-2, and predict the individual-level protective effectiveness conferred by natural infections with the Delta and the Omicron B.1.1.529 variants, and by the BioNTech-Pfizer (BNT162b2), Oxford-AstraZeneca (ChAdOx1), and 3rd-dose mRNA booster vaccines, against outcomes for both Delta and Omicron. We also demonstrate a use case of the model in late 2021 during the emergence of Omicron, showing how the model can be rapidly updated with emerging epidemiological data on multiple variants in the same population, to infer key immunogenicity and intrinsic transmissibility characteristics of the new variant, before the former can be more directly observed via vaccine effectiveness data.
This model provided timely inference on rapidly evolving epidemic situations of significant concern during the early stages of the COVID-19 pandemic. The general nature of the model enables it to be used to support management of a range of infectious diseases.
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从人群水平的有效性数据中预测对传染病结果的免疫保护作用,并将其应用于 COVID-19。
量化以前的感染和接种疫苗对未来感染或疾病后果的保护程度,对于管理传染病的传播和后果至关重要。我们提出了一个通用的统计模型,用于预测不同免疫暴露(疫苗和感染的数量、类型和菌株)所赋予的保护强度,针对多种感兴趣的结果,同时考虑到免疫减弱。我们预测针对关键临床结果的免疫保护:出现症状、住院和死亡。我们还预测了与传播相关的结果:获得感染和突破性感染的进一步传播。这些方法可以量化免疫对人群层面传播动态的影响。我们的模型利用人口水平的数据(如疫苗有效性估计)和中和抗体水平(作为保护的相关因素)来校准免疫保护水平。这使得模型能够学习超越抗体动力学或其他相关因素单独预测的已实现免疫水平。我们展示了该模型在SARS-CoV-2中的应用,并预测了Delta和Omicron B.1.1.529变体自然感染、BioNTech-Pfizer (BNT162b2)、Oxford-AstraZeneca (ChAdOx1)和第三剂量mRNA加强疫苗对Delta和Omicron结果的个体水平保护效果。我们还在2021年末展示了该模型在Omicron出现期间的一个用例,展示了如何使用同一人群中多个变体的新流行病学数据快速更新该模型,以推断新变体的关键免疫原性和内在传播性特征,然后通过疫苗有效性数据更直接地观察到前者。该模型对COVID-19大流行早期阶段快速演变的重大疫情提供了及时的推断。该模型的一般性质使其能够用于支持对一系列传染病的管理。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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