Department of Zoology, University of Oxford, Oxford, UK.
Independent Consultant, London, England.
BMC Med. 2021 Jan 12;19(1):19. doi: 10.1186/s12916-020-01887-1.
Cross-reactivity to SARS-CoV-2 from exposure to endemic human coronaviruses (eHCoV) is gaining increasing attention as a possible driver of both protection against infection and COVID-19 severity. Here we explore the potential role of cross-reactivity induced by eHCoVs on age-specific COVID-19 severity in a mathematical model of eHCoV and SARS-CoV-2 transmission.
We use an individual-based model, calibrated to prior knowledge of eHCoV dynamics, to fully track individual histories of exposure to eHCoVs. We also model the emergent dynamics of SARS-CoV-2 and the risk of hospitalisation upon infection.
We hypothesise that primary exposure with any eHCoV confers temporary cross-protection against severe SARS-CoV-2 infection, while life-long re-exposure to the same eHCoV diminishes cross-protection, and increases the potential for disease severity. We show numerically that our proposed mechanism can explain age patterns of COVID-19 hospitalisation in EU/EEA countries and the UK. We further show that some of the observed variation in health care capacity and testing efforts is compatible with country-specific differences in hospitalisation rates under this model.
This study provides a "proof of possibility" for certain biological and epidemiological mechanisms that could potentially drive COVID-19-related variation across age groups. Our findings call for further research on the role of cross-reactivity to eHCoVs and highlight data interpretation challenges arising from health care capacity and SARS-CoV-2 testing.
由于接触地方性人类冠状病毒 (eHCoV) 而对 SARS-CoV-2 产生交叉反应,作为预防感染和 COVID-19 严重程度的可能驱动因素,正引起越来越多的关注。在这里,我们在 eHCoV 和 SARS-CoV-2 传播的数学模型中探索了 eHCoV 引起的交叉反应对特定年龄 COVID-19 严重程度的潜在作用。
我们使用基于个体的模型,根据对 eHCoV 动力学的先验知识进行校准,以全面跟踪个体接触 eHCoV 的历史。我们还对 SARS-CoV-2 的突发动态和感染后的住院风险进行建模。
我们假设,初次接触任何 eHCoV 都会暂时对严重的 SARS-CoV-2 感染提供交叉保护,而终生反复接触相同的 eHCoV 则会降低交叉保护,并增加疾病严重程度的可能性。我们通过数值表明,我们提出的机制可以解释欧盟/欧洲经济区国家和英国 COVID-19 住院的年龄模式。我们进一步表明,在这种模型下,观察到的一些医疗保健能力和检测工作的差异与特定国家的住院率差异是一致的。
本研究为可能驱动 COVID-19 相关年龄组差异的某些生物学和流行病学机制提供了“可能性证明”。我们的研究结果呼吁进一步研究 eHCoV 交叉反应的作用,并强调了医疗保健能力和 SARS-CoV-2 检测带来的数据分析挑战。