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本文引用的文献

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Mathematical modeling of viral kinetics under immune control during primary HIV-1 infection.原发性 HIV-1 感染期间免疫控制下病毒动力学的数学建模。
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Dynamics of immune escape during HIV/SIV infection.HIV/SIV感染期间免疫逃逸的动态变化
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The probability of HIV infection in a new host and its reduction with microbicides.新宿主感染HIV的概率及其通过杀微生物剂的降低情况。
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Modeling HIV quasispecies evolutionary dynamics.模拟HIV准种进化动力学。
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The type-reproduction number T in models for infectious disease control.传染病控制模型中的类型繁殖数T
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A stochastic model of cytotoxic T cell responses.细胞毒性T细胞反应的随机模型。
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A new method for estimating the effort required to control an infectious disease.一种估算控制传染病所需努力的新方法。
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Mechanisms of enveloped RNA virus budding.包膜RNA病毒出芽的机制。
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病毒和免疫系统动力学的随机模型。

Stochastic models for virus and immune system dynamics.

机构信息

Department of Mathematics, Texas Tech University, Lubbock, TX 79409, USA.

出版信息

Math Biosci. 2011 Dec;234(2):84-94. doi: 10.1016/j.mbs.2011.08.007. Epub 2011 Sep 16.

DOI:10.1016/j.mbs.2011.08.007
PMID:21945381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3249397/
Abstract

New stochastic models are developed for the dynamics of a viral infection and an immune response during the early stages of infection. The stochastic models are derived based on the dynamics of deterministic models. The simplest deterministic model is a well-known system of ordinary differential equations which consists of three populations: uninfected cells, actively infected cells, and virus particles. This basic model is extended to include some factors of the immune response related to Human Immunodeficiency Virus-1 (HIV-1) infection. For the deterministic models, the basic reproduction number, R0, is calculated and it is shown that if R0<1, the disease-free equilibrium is locally asymptotically stable and is globally asymptotically stable in some special cases. The new stochastic models are systems of stochastic differential equations (SDEs) and continuous-time Markov chain (CTMC) models that account for the variability in cellular reproduction and death, the infection process, the immune system activation, and viral reproduction. Two viral release strategies are considered: budding and bursting. The CTMC model is used to estimate the probability of virus extinction during the early stages of infection. Numerical simulations are carried out using parameter values applicable to HIV-1 dynamics. The stochastic models provide new insights, distinct from the basic deterministic models. For the case R0>1, the deterministic models predict the viral infection persists in the host. But for the stochastic models, there is a positive probability of viral extinction. It is shown that the probability of a successful invasion depends on the initial viral dose, whether the immune system is activated, and whether the release strategy is bursting or budding.

摘要

新的随机模型是为感染早期的病毒感染和免疫反应动力学开发的。随机模型是基于确定性模型的动力学推导出来的。最简单的确定性模型是一个著名的常微分方程系统,由三个群体组成:未感染的细胞、活跃感染的细胞和病毒颗粒。这个基本模型扩展到包括与人类免疫缺陷病毒-1(HIV-1)感染相关的一些免疫反应因素。对于确定性模型,计算了基本再生数 R0,并表明如果 R0<1,则无病平衡点在局部渐近稳定,在某些特殊情况下在全局渐近稳定。新的随机模型是随机微分方程(SDE)和连续时间马尔可夫链(CTMC)模型的系统,这些模型考虑了细胞繁殖和死亡、感染过程、免疫系统激活和病毒繁殖的可变性。考虑了两种病毒释放策略:出芽和爆发。CTMC 模型用于估计感染早期病毒灭绝的概率。使用适用于 HIV-1 动力学的参数值进行数值模拟。随机模型提供了不同于基本确定性模型的新见解。对于 R0>1 的情况,确定性模型预测病毒感染会在宿主中持续存在。但对于随机模型,病毒灭绝的可能性很大。结果表明,成功入侵的概率取决于初始病毒剂量、免疫系统是否激活以及释放策略是出芽还是爆发。