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本文引用的文献

1
A Multi-Compartment Hybrid Computational Model Predicts Key Roles for Dendritic Cells in Tuberculosis Infection.一种多室混合计算模型预测树突状细胞在结核感染中的关键作用。
Computation (Basel). 2016;4(4). doi: 10.3390/computation4040039. Epub 2016 Oct 21.
2
Comparing efficacies of moxifloxacin, levofloxacin and gatifloxacin in tuberculosis granulomas using a multi-scale systems pharmacology approach.使用多尺度系统药理学方法比较莫西沙星、左氧氟沙星和加替沙星在结核肉芽肿中的疗效。
PLoS Comput Biol. 2017 Aug 17;13(8):e1005650. doi: 10.1371/journal.pcbi.1005650. eCollection 2017 Aug.
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An in silico model of the effects of vitamin D3 on mycobacterium infected macrophage.维生素D3对感染分枝杆菌的巨噬细胞影响的计算机模拟模型。
Annu Int Conf IEEE Eng Med Biol Soc. 2016 Aug;2016:1443-1446. doi: 10.1109/EMBC.2016.7590980.
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How to Use a Chemotherapeutic Agent When Resistance to It Threatens the Patient.当患者面临化疗药物耐药威胁时如何使用该化疗药物。
PLoS Biol. 2017 Feb 9;15(2):e2001110. doi: 10.1371/journal.pbio.2001110. eCollection 2017 Feb.
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New concepts in understanding latent tuberculosis.理解潜伏性结核病的新概念。
Curr Opin Infect Dis. 2017 Jun;30(3):316-321. doi: 10.1097/QCO.0000000000000367.
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Identifying patients at high risk of tuberculosis recurrence.识别结核病复发高危患者。
Int J Mycobacteriol. 2016 Dec;5 Suppl 1:S66. doi: 10.1016/j.ijmyco.2016.08.017. Epub 2016 Sep 21.
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Correlates of tuberculosis risk: predictive biomarkers for progression to active tuberculosis.结核病风险的相关因素:进展为活动性结核病的预测生物标志物
Eur Respir J. 2016 Dec;48(6):1751-1763. doi: 10.1183/13993003.01012-2016. Epub 2016 Nov 11.
8
The Global Burden of Latent Tuberculosis Infection: A Re-estimation Using Mathematical Modelling.潜伏性结核感染的全球负担:使用数学模型的重新估计
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9
Granuloma formation in leishmaniasis: A mathematical model.利什曼病中的肉芽肿形成:一个数学模型。
J Theor Biol. 2017 Jan 7;412:48-60. doi: 10.1016/j.jtbi.2016.10.004. Epub 2016 Oct 18.
10
TB vaccines in clinical development.处于临床开发阶段的结核病疫苗。
Tuberculosis (Edinb). 2016 Aug;99 Suppl 1:S16-20. doi: 10.1016/j.tube.2016.05.013. Epub 2016 Jun 16.

关于计算和数学建模对我们理解结核分枝杆菌宿主内感染及治疗所做贡献的综述。

A review of computational and mathematical modeling contributions to our understanding of Mycobacterium tuberculosis within-host infection and treatment.

作者信息

Kirschner Denise, Pienaar Elsje, Marino Simeone, Linderman Jennifer J

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI.

Department of Chemical Engineering, University of Michigan, Ann Arbor, MI.

出版信息

Curr Opin Syst Biol. 2017 Jun;3:170-185. doi: 10.1016/j.coisb.2017.05.014. Epub 2017 May 22.

DOI:10.1016/j.coisb.2017.05.014
PMID:30714019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6354243/
Abstract

Tuberculosis (TB) is an ancient and deadly disease characterized by complex host-pathogen dynamics playing out over multiple time and length scales and physiological compartments. Computational modeling can be used to integrate various types of experimental data and suggest new hypotheses, mechanisms, and therapeutic approaches to TB. Here, we offer a first-time comprehensive review of work on within-host TB models that describe the immune response of the host to infection, including the formation of lung granulomas. The models include systems of ordinary and partial differential equations and agent-based models as well as hybrid and multi-scale models that are combinations of these. Many aspects of infection, including host dynamics in the lung (typical site of infection for TB), granuloma formation, roles of cytokine and chemokine dynamics, and bacterial nutrient availability have been explored. Finally, we survey applications of these within-host models to TB therapy and prevention and suggest future directions to impact this global disease.

摘要

结核病(TB)是一种古老且致命的疾病,其特征在于复杂的宿主 - 病原体动态变化,这种变化在多个时间和长度尺度以及生理隔室中展开。计算建模可用于整合各种类型的实验数据,并提出有关结核病的新假设、机制和治疗方法。在此,我们首次全面综述了关于宿主内结核病模型的研究工作,这些模型描述了宿主对感染的免疫反应,包括肺肉芽肿的形成。这些模型包括常微分方程和偏微分方程系统、基于主体的模型,以及这些模型的组合——混合模型和多尺度模型。感染的许多方面,包括肺部(结核病的典型感染部位)的宿主动态、肉芽肿形成、细胞因子和趋化因子动态的作用以及细菌营养可用性等,都已得到探索。最后,我们考察了这些宿主内模型在结核病治疗和预防方面的应用,并提出了影响这种全球性疾病的未来方向。