Ruggiero Steve M, Pilvankar Minu R, Ford Versypt Ashlee N
School of Chemical Engineering, Oklahoma State University, Stillwater, OK 74078, USA.
Oklahoma Center for Respiratory and Infectious Diseases, Oklahoma State University, Stillwater, OK 74078, USA.
Processes (Basel). 2017 Dec;5(4). doi: 10.3390/pr5040079. Epub 2017 Dec 11.
Tuberculosis (TB) is one of the most common infectious diseases worldwide. It is estimated that one-third of the world's population is infected with TB. Most have the latent stage of the disease that can later transition to active TB disease. TB is spread by aerosol droplets containing Mycobacterium tuberculosis (Mtb). Mtb bacteria enter through the respiratory system and are attacked by the immune system in the lungs. The bacteria are clustered and contained by macrophages into cellular aggregates called granulomas. These granulomas can hold the bacteria dormant for long periods of time in latent TB. The bacteria can be perturbed from latency to active TB disease in a process called granuloma activation when the granulomas are compromised by other immune response events in a host, such as HIV, cancer, or aging. Dysregulation of matrix metalloproteinase 1 (MMP-1) has been recently implicated in granuloma activation through experimental studies, but the mechanism is not well understood. Animal and human studies currently cannot probe the dynamics of activation, so a computational model is developed to fill this gap. This dynamic mathematical model focuses specifically on the latent to active transition after the initial immune response has successfully formed a granuloma. Bacterial leakage from latent granulomas is successfully simulated in response to the MMP-1 dynamics under several scenarios for granuloma activation.
结核病是全球最常见的传染病之一。据估计,全球三分之一的人口感染了结核杆菌。大多数人处于疾病的潜伏期,之后可能会转变为活动性结核病。结核病通过含有结核分枝杆菌(Mtb)的气溶胶飞沫传播。Mtb细菌通过呼吸系统进入人体,并在肺部受到免疫系统的攻击。这些细菌被巨噬细胞聚集并包裹在称为肉芽肿的细胞聚集体中。在潜伏性结核病中,这些肉芽肿可以使细菌长时间处于休眠状态。当肉芽肿因宿主中的其他免疫反应事件(如艾滋病毒、癌症或衰老)而受损时,细菌可以在一个称为肉芽肿激活的过程中从潜伏期转变为活动性结核病。最近的实验研究表明,基质金属蛋白酶1(MMP-1)的失调与肉芽肿激活有关,但其机制尚不清楚。目前,动物和人体研究无法探究激活的动态过程,因此开发了一个计算模型来填补这一空白。这个动态数学模型特别关注在初始免疫反应成功形成肉芽肿后从潜伏到激活的转变。在几种肉芽肿激活的情况下,针对MMP-1动态模拟了潜伏肉芽肿中的细菌泄漏。