Department of Mathematical and Statistical Sciences, University of Alberta, Edmonton, AB T6G 2R3, Canada.
Collaborative Mathematical Biology Group, University of Alberta, Edmonton, AB T6G 2R3, Canada.
Viruses. 2021 Sep 13;13(9):1815. doi: 10.3390/v13091815.
We introduce an explicit function that describes virus-load curves on a patient-specific level. This function is based on simple and intuitive model parameters. It allows virus load analysis of acute viral infections without solving a full virus load dynamic model. We validate our model on data from mice influenza A, human rhinovirus data, human influenza A data, and monkey and human SARS-CoV-2 data. We find wide distributions for the model parameters, reflecting large variability in the disease outcomes between individuals. Further, we compare the virus load function to an established of virus dynamics, and we provide a new way to estimate the exponential growth rates of the corresponding infection phases. The virus load function, the target model, and the exponential approximations show excellent fits for the data considered. Our virus-load function offers a new way to analyze patient-specific virus load data, and it can be used as input for higher level models for the physiological effects of a virus infection, for models of tissue damage, and to estimate patient risks.
我们介绍了一个可以描述患者个体水平上病毒载量曲线的显式函数。这个函数基于简单直观的模型参数。它可以在不求解完整病毒载量动态模型的情况下,对急性病毒感染进行病毒载量分析。我们在来自小鼠流感 A、人类鼻病毒、人类流感 A 和猴和人 SARS-CoV-2 的数据上验证了我们的模型。我们发现模型参数的分布很广,反映了个体之间疾病结局的很大差异。此外,我们还将病毒载量函数与已建立的病毒动力学模型进行了比较,并提供了一种新的方法来估计相应感染阶段的指数增长率。所考虑的数据与病毒载量函数、目标模型和指数近似值的拟合非常好。我们的病毒载量函数为分析患者特定的病毒载量数据提供了一种新的方法,它可以用作更高层次的病毒感染生理效应模型、组织损伤模型和估计患者风险的模型的输入。