肺结核
结核分枝杆菌
氧气
肉芽肿
缺氧(环境)
氧气输送
扩散
免疫系统
免疫学
生物
化学
医学
病理
物理
热力学
有机化学
作者
Meenal Datta,Laura E. Via,Wei Chen,James W. Baish,Lei Xu,Clifton E. Barry,Rakesh K. Jain
标识
DOI:10.1007/s10439-015-1415-3
摘要
Pulmonary granulomas—the hallmark of Mycobacterium tuberculosis (MTB) infection—are dense cellular lesions that often feature regions of hypoxia and necrosis, partially due to limited transport of oxygen. Low oxygen in granulomas can impair the host immune response, while MTB are able to adapt and persist in hypoxic environments. Here, we used a physiologically based mathematical model of oxygen diffusion and consumption to calculate oxygen profiles within the granuloma, assuming Michaelis–Menten kinetics. An approximate analytical solution—using a priori and newly estimated parameters from experimental data in a rabbit model of tuberculosis—was able to predict the size of hypoxic and necrotic regions in agreement with experimental results from the animal model. Such quantitative understanding of transport limitations can inform future tuberculosis therapeutic strategies that may include adjunct host-directed therapies that facilitate oxygen and drug delivery for more effective treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI