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多波疫情的随机模型:将增长分解为固有易感性和外部传染性分布。

Stochastic formulation of multiwave pandemic: decomposition of growth into inherent susceptibility and external infectivity distributions.

作者信息

Mukherjee Saumyak, Mondal Sayantan, Bagchi Biman

机构信息

Solid State and Structural Chemistry Unit, Indian Institute of Science, Bengaluru, India.

Present Address: Department of Chemistry and Biochemistry, Ruhr-Universität Bochum, Universitätsstraße 150, 44801 Bochum, Germany.

出版信息

J Chem Sci (Bangalore). 2021;133(4):118. doi: 10.1007/s12039-021-01981-8. Epub 2021 Nov 18.

Abstract

Many known and unknown factors play significant roles in the persistence of an infectious disease, but two that are often ignored in theoretical modelling are the distributions of (i) ( ) and (ii) ( ), in a population. While the former is determined by the immunity of an individual towards a disease, the latter depends on the exposure of a susceptible person to the infection. using a modified SAIR (Susceptible-Asymptomatic-Infected-Removed) model to include these two distributions. The resulting integro-differential equations are solved using Kinetic Monte Carlo Cellular Automata (KMC-CA) simulations. Ω infection occurs only if the value of Ω is greater than a Pandemic Infection Parameter (PIP), . Not only does this parameter provide a microscopic viewpoint of the reproduction number R advocated by the conventional SIR model, but it also takes into consideration the viral load experienced by a susceptible person. We find that the neglect of this coupling could compromise quantitative predictions and lead to incorrect estimates of the infections required to achieve the herd immunity threshold. The figure represents the network model for spread of infectious diseases considered in this work. It also shows the resultant multiwave infection graph by inclusion of inherent susceptibility and external infectivity distributions and migration of infected individuals.

摘要

许多已知和未知因素在传染病的持续传播中起着重要作用,但在理论建模中经常被忽视的两个因素是:(i)( )和(ii)( )在人群中的分布。前者由个体对疾病的免疫力决定,而后者则取决于易感人群接触感染源的情况。我们使用改进的SAIR(易感-无症状-感染-康复)模型来纳入这两种分布。由此产生的积分-微分方程通过动力学蒙特卡洛细胞自动机(KMC-CA)模拟求解。仅当Ω的值大于大流行感染参数(PIP) 时才会发生感染。该参数不仅提供了传统SIR模型所倡导的繁殖数R的微观视角,还考虑了易感人群所经历的病毒载量。我们发现,忽略这种耦合可能会影响定量预测,并导致对实现群体免疫阈值所需感染人数的估计错误。该图表示了本研究中所考虑的传染病传播网络模型。它还展示了通过纳入固有易感性和外部传染性分布以及感染个体的迁移而产生的多波感染图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a85/8600499/30d7625e7f2c/12039_2021_1981_Figa_HTML.jpg

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