利用分子通讯模拟多种促炎细胞因子的影响

Shivam Thakker, Dhaval K. Patel, Kathan S. Joshi, M. López-Benítez
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引用次数: 1

摘要

近年来,由于分子通信在医疗保健领域的广泛应用和许多其他新领域的发展,它已成为一个重要的研究领域。本文提出了一种基于分子通讯的SARS-CoV2病毒在人体内传播模型。这种病毒利用ACE2受体作为进入血管和器官的通道,然后进行自我复制。在对感染的反应中,免疫系统合成促炎细胞因子,如IL6、IL2和TNFa。这种积极的身体反应可能会被产生抗炎细胞因子如il - 4和il - 10进一步损害。我们还提出了一个基于流动的分子通信系统的数学模型,该模型使用马尔可夫状态转换,有助于检测这些促炎细胞因子水平,并通过考虑多种细胞因子对体内感染进行进一步推断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modelling the Impact of Multiple Pro-inflammatory Cytokines Using Molecular Communication
Motivated by various health care applications and many other novel fields of Molecular Communication (MC), it has become an important field of research since the last decade. This paper proposes a molecular communication-based model for the spread of the SARS-CoV2 virus in the human body. The virus uses the ACE2 receptor as a gateway to enter the blood vessels, organs and then replicate itself. In response to the infection, the immune system synthesizes pro-inflammatory cytokines such as IL6, IL2, and TNFa. This active bodily response may be further compromised by the generation of anti-inflammatory cytokines such as IL4 and IL10. We also propose a mathematical model using a Markov state transition for a flow-based molecular communication system which contributes to the detection of these pro-inflammatory cytokines level and gives a further inference about the infection in the body by taking multiple cytokines into account.
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