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先天免疫在SEIS流行病模型中的作用的动态分析

Dynamic analysis of the role of innate immunity in SEIS epidemic model.

作者信息

Jain Shikha, Kumar Sachin

机构信息

Department of Mathematics, University of Delhi, Delhi, New Delhi 110007 India.

出版信息

Eur Phys J Plus. 2021;136(4):439. doi: 10.1140/epjp/s13360-021-01390-3. Epub 2021 Apr 23.

DOI:10.1140/epjp/s13360-021-01390-3
PMID:33936924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8064703/
Abstract

Consideration of every important aspect while modeling a disease makes the model more precise and the disease eradication strategy more powerful. In the present paper, we analyze the importance of innate immunity on SEIS modeling. We propose an SEIS model with Holling type II and type III functions representing innate immunity. We find the existence and stability conditions for the equilibria. When innate immunity is in the form of Holling type II function, the disease-free equilibrium exists for reproduction number less than unity and is locally asymptotically stable, and supercritical transcritical (forward) as well as subcritical transcritical (backward) bifurcation may occur where the contact rate acts as the bifurcation parameter. Hence, disease-free equilibrium need not be globally stable. For reproduction number greater than unity unique endemic equilibrium exists which is locally asymptotically stable. The global stability conditions for the same are deduced with the help of Lozinski measure. When innate immunity is considered a Holling type III function, the disease-free equilibrium point exists for reproduction number less than unity and is locally as well as globally stable. The existence of either unique or multiple endemic equilibria is found when reproduction number is greater than unity, and there exists at least one locally asymptotically stable equilibrium point and bistability can also be encountered. The conditions for the existence of Andronov-Hopf bifurcation are deduced for both cases. Moreover, we observe that ignoring innate immunity annihilates the possibility of Andronov-Hopf bifurcation. Numerical simulation is performed to validate the mathematical findings. Comparing the obtained results to the case when innate immunity is ignored, it is deduced that ignoring it ends the possibility of backward bifurcation, Andronov-Hopf bifurcation as well as the existence of multiple equilibria, and it also leads to the prediction of higher infection than the actual which may deflect the accuracy of the model to a high extent. This would further lead to false predictions and inefficient disease control strategies which in turn would make disease eradication a difficult and more expensive task.

摘要

在对疾病进行建模时考虑到每一个重要方面会使模型更加精确,疾病根除策略更加强有力。在本文中,我们分析了固有免疫在SEIS模型中的重要性。我们提出了一个具有表示固有免疫的Holling II型和III型函数的SEIS模型。我们找到了平衡点的存在性和稳定性条件。当固有免疫呈Holling II型函数形式时,对于小于1的繁殖数,无病平衡点存在且局部渐近稳定,并且当接触率作为分岔参数时,可能会出现超临界跨临界(向前)以及亚临界跨临界(向后)分岔。因此,无病平衡点不一定是全局稳定的。对于大于1的繁殖数,存在唯一的地方病平衡点,它是局部渐近稳定的。借助Lozinski测度推导出了其全局稳定性条件。当固有免疫被视为Holling III型函数时,对于小于1的繁殖数,无病平衡点存在且局部和全局稳定。当繁殖数大于1时,发现存在唯一或多个地方病平衡点,并且至少存在一个局部渐近稳定的平衡点,还可能出现双稳性。推导了两种情况下安德罗诺夫 - 霍普夫分岔存在的条件。此外,我们观察到忽略固有免疫消除了安德罗诺夫 - 霍普夫分岔的可能性。进行了数值模拟以验证数学结果。将所得结果与忽略固有免疫的情况进行比较,推断出忽略它会消除向后分岔、安德罗诺夫 - 霍普夫分岔以及多个平衡点存在的可能性,并且还会导致预测的感染率高于实际情况,这可能在很大程度上使模型的准确性产生偏差。这将进一步导致错误的预测和低效的疾病控制策略,并进而使疾病根除成为一项困难且成本更高的任务。

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本文引用的文献

1
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Commun Nonlinear Sci Numer Simul. 2020 Sep;88:105312. doi: 10.1016/j.cnsns.2020.105312. Epub 2020 Apr 30.
2
SEIR model for COVID-19 dynamics incorporating the environment and social distancing.纳入环境因素和社交距离的COVID-19动态SEIR模型。
BMC Res Notes. 2020 Jul 23;13(1):352. doi: 10.1186/s13104-020-05192-1.
3
An SEI infection model incorporating media impact.一个纳入媒体影响的性传播感染(SEI)模型。
流感感染与疫苗接种中的系统复杂性:对冬季超额死亡率的影响。
Infect Dis Rep. 2022 Apr 21;14(3):287-309. doi: 10.3390/idr14030035.
4
Endemic state equivalence between non-Markovian SEIS and Markovian SIS model in complex networks.复杂网络中非马尔可夫SEIS模型与马尔可夫SIS模型之间的地方病状态等价性
Physica A. 2022 Aug 1;599:127480. doi: 10.1016/j.physa.2022.127480. Epub 2022 Apr 30.
5
Dynamical analysis of SEIS model with nonlinear innate immunity and saturated treatment.具有非线性先天免疫和饱和治疗的SEIS模型的动力学分析
Eur Phys J Plus. 2021;136(9):952. doi: 10.1140/epjp/s13360-021-01944-5. Epub 2021 Sep 17.
Math Biosci Eng. 2017;14(5-6):1317-1335. doi: 10.3934/mbe.2017068.
4
Cellular Innate Immunity: An Old Game with New Players.细胞固有免疫:一场有新参与者的古老博弈。
J Innate Immun. 2017;9(2):111-125. doi: 10.1159/000453397. Epub 2016 Dec 23.
5
Mathematical Model of Innate and Adaptive Immunity of Sepsis: A Modeling and Simulation Study of Infectious Disease.脓毒症先天性和适应性免疫的数学模型:传染病的建模与仿真研究
Biomed Res Int. 2015;2015:504259. doi: 10.1155/2015/504259. Epub 2015 Sep 8.
6
On the computational modeling of the innate immune system.关于先天免疫系统的计算建模。
BMC Bioinformatics. 2013;14 Suppl 6(Suppl 6):S7. doi: 10.1186/1471-2105-14-S6-S7. Epub 2013 Apr 17.
7
Analysis of a tuberculosis model with a case study in Uganda.分析一个有乌干达案例研究的结核病模型。
J Biol Dyn. 2010 Nov;4(6):571-93. doi: 10.1080/17513750903518441.
8
Dynamical models of tuberculosis and their applications.结核动态模型及其应用。
Math Biosci Eng. 2004 Sep;1(2):361-404. doi: 10.3934/mbe.2004.1.361.
9
The construction of next-generation matrices for compartmental epidemic models.构建用于隔室流行病模型的下一代矩阵。
J R Soc Interface. 2010 Jun 6;7(47):873-85. doi: 10.1098/rsif.2009.0386. Epub 2009 Nov 5.
10
Implications of vaccination and waning immunity.疫苗接种及免疫力减弱的影响。
Proc Biol Sci. 2009 Jun 7;276(1664):2071-80. doi: 10.1098/rspb.2009.0057. Epub 2009 Mar 4.