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首页> 外文期刊>Theoretical Biology and Medical Modelling >Improving the estimation of the death rate of infected cells from time course data during the acute phase of virus infections: application to acute HIV-1 infection in a humanized mouse model
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Improving the estimation of the death rate of infected cells from time course data during the acute phase of virus infections: application to acute HIV-1 infection in a humanized mouse model

机译:从病毒感染急性期的时程数据改进对感染细胞死亡率的估计:在人源化小鼠模型中应用于急性HIV-1感染

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Background Mathematical modeling of virus dynamics has provided quantitative insights into viral infections such as influenza, the simian immunodeficiency virus/human immunodeficiency virus, hepatitis B, and hepatitis C. Through modeling, we can estimate the half-life of infected cells, the exponential growth rate, and the basic reproduction number (R0). To calculate R0 from virus load data, the death rate of productively infected cells is required. This can be readily estimated from treatment data collected during the chronic phase, but is difficult to determine from acute infection data. Here, we propose two new models that can reliably estimate the average life span of infected cells from acute-phase data, and apply both methods to experimental data from humanized mice infected with HIV-1. Methods Both new models, called as the reduced quasi-steady state (RQS) model and the piece-wise regression (PWR) model, are derived by simplification of a standard model for the acute-phase dynamics of target cells, viruses and infected cells. By having only a limited number of parameters, both models allow us to reliably estimate the death rate of productively infected cells. Simulated datasets with plausible parameter values are generated with the standard model to compare the performance of the new models with that of the major previous model (i.e., the simple exponential model). Finally, we fit models to time course data from HIV-1 infected humanized mice to estimate the several important parameters characterizing their acute infection. Results and conclusions The new models provided much better estimates than the previous model because they more precisely capture the de novo infection process. Both models describe the acute phase of HIV-1 infected humanized mice reasonably well, and we estimated an average death rate of infected cells of 0.61 and 0.61, an average exponential growth rate of 0.69 and 0.76, and an average basic reproduction number of 2.30 and 2.38 in the RQS model and the PWR model, respectively. These estimates are fairly close to those obtained in humans.
机译:背景技术病毒动力学的数学建模提供了对病毒感染(如流感病毒,猿猴免疫缺陷病毒/人类免疫缺陷病毒,乙型肝炎和丙型肝炎)的定量见解。通过建模,我们可以估算受感染细胞的半衰期,指数增长速率和基本再现数(R 0 )。要从病毒载量数据计算R 0 ,需要有效感染细胞的死亡率。从慢性期收集的治疗数据可以很容易地估计出这一点,但是很难从急性感染数据中确定。在这里,我们提出了两个新模型,它们可以根据急性期数据可靠地估计感染细胞的平均寿命,并将这两种方法都应用于感染HIV-1的人源化小鼠的实验数据。方法通过简化目标细胞,病毒和感染细胞急性期动力学的标准模型,可以得出两种新模型,分别称为简化拟稳态(RQS)模型和分段回归(PWR)模型。 。通过仅使用有限数量的参数,这两个模型都使我们能够可靠地估计生产性感染细胞的死亡率。使用标准模型生成具有合理参数值的模拟数据集,以将新模型的性能与以前的主要模型(即简单指数模型)的性能进行比较。最后,我们将模型拟合到HIV-1感染的人源化小鼠的时程数据中,以估计表征其急性感染的几个重要参数。结果与结论新模型提供了比以前模型更好的估计,因为它们可以更精确地捕获从头感染过程。两种模型都很好地描述了被HIV-1感染的人源化小鼠的急性期,我们估计感染细胞的平均死亡率为0.61和0.61,平均指数增长率为0.69和0.76,平均基本繁殖数为2.30和RQS模型和PWR模型分别为2.38。这些估计非常接近于人类获得的估计。

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