Leicester Tuberculosis Research Group (LTBRG), Department of Infection Immunity and Inflammation, University of Leicester, University Road, Leicester LE1 7RH, UK.
Cell Mol Immunol. 2018 Mar;15(3):226-232. doi: 10.1038/cmi.2017.145. Epub 2018 Jan 29.
Accurate prediction of which patient will progress from a sub-clinical Mycobacterium tuberculosis infection to active tuberculosis represents an elusive, yet critical, clinical research objective. From the individual perspective, progression can be considered to be the product of a series of unfortunate events or even a run of bad luck. Here, we identify the subtle physiological relationships that can influence the odds of progression to active TB and how this progression may reflect directed dysbiosis in a number of interrelated systems. Most infected individuals who progress to disease have apparently good immune responses, but these responses are, at times, compromised by either local or systemic environmental factors. Obvious disease promoting processes, such as tissue-damaging granulomata, usually manifest in the lung, but illness is systemic. This apparent dichotomy between local and systemic reflects a clear need to define the factors that promote progression to active disease within the context of the body as a physiological whole. We discuss aspects of the host environment that can impact expression of immunity, including the microbiome, glucocorticoid-mediated regulation, catecholamines and interaction between the gut, liver and lung. We suggest the importance of integrating precision medicine into our analyses of experimental outcomes such that apparently conflicting results are not contentious, but rather reflect the impact of these subtle relationships with our environment and microbiota.
准确预测哪些患者会从潜伏性结核分枝杆菌感染发展为活动性结核病,这是一个难以捉摸但至关重要的临床研究目标。从个体角度来看,进展可以被认为是一系列不幸事件的产物,甚至是一连串的厄运。在这里,我们确定了可以影响向活动性结核病进展几率的微妙生理关系,以及这种进展如何反映出许多相互关联的系统中的定向失调。大多数进展为疾病的感染者显然有良好的免疫反应,但这些反应有时会因局部或全身环境因素而受到损害。明显的促病过程,如组织损伤性肉芽肿,通常在肺部表现出来,但疾病是全身性的。这种局部和全身之间的明显二分法清楚地表明,需要在整个身体的生理整体背景下定义促进向活动性疾病进展的因素。我们讨论了宿主环境中可以影响免疫表达的因素,包括微生物组、糖皮质激素介导的调节、儿茶酚胺以及肠道、肝脏和肺部之间的相互作用。我们认为将精准医学纳入我们对实验结果的分析的重要性,使得看似矛盾的结果不再有争议,而是反映了这些与我们的环境和微生物组的微妙关系的影响。