Department of Systems Immunology and Braunschweig Integrated Centre of Systems Biology, Helmholtz Centre for Infection Research, Rebenring 56, 38106 Braunschweig, Germany.
Laboratory of Experimental Rheumatology and Neuroendocrine Immunology, Department of Internal Medicine, University Hospital Regensburg, 93042 Regensburg, Germany.
J R Soc Interface. 2022 Jun;19(191):20220206. doi: 10.1098/rsif.2022.0206. Epub 2022 Jun 22.
Different parts of an organism like the gut, endocrine, nervous and immune systems constantly exchange information. Understanding the pathogenesis of various systemic chronic diseases increasingly relies on understanding how these subsystems orchestrate their activities.
We started from the working hypothesis that energy is a fundamental quantity that governs activity levels of all subsystems and that interactions between subsystems control the distribution of energy according to acute needs. Based on physiological knowledge, we constructed a mathematical model for the energy flow between subsystems and analysed the resulting organismal responses to infections.
The model reproduces common behaviour in acute infections and suggests several host parameters that modulate infection duration and therapeutic responsiveness. Moreover, the model allows the formulation of conditions for the induction of chronic infections and predicts that alterations in energy released from fat can lead to the transition from clearance of acute infections to a chronic inflammatory state.
These results suggest a fundamental role for brain and fat in controlling immune response through systemic energy control. In particular, it suggests that lipolysis resistance, which is known to be involved in obesity and ageing, might be a survival programme for coping with chronic infections.
生物体的不同部位,如肠道、内分泌、神经和免疫系统,不断地交换信息。理解各种系统性慢性疾病的发病机制越来越依赖于理解这些子系统如何协调它们的活动。
我们从工作假说出发,即能量是控制所有子系统活动水平的基本数量,子系统之间的相互作用根据急性需求控制能量的分布。基于生理学知识,我们构建了一个子系统之间能量流动的数学模型,并分析了由此产生的机体对感染的反应。
该模型再现了急性感染中的常见行为,并提出了几个宿主参数,这些参数可以调节感染持续时间和治疗反应性。此外,该模型还可以为慢性感染的诱导条件提供依据,并预测从急性感染清除到慢性炎症状态的转变可能是由于脂肪释放的能量发生改变。
这些结果表明,大脑和脂肪通过全身能量控制在控制免疫反应方面起着基础性作用。特别是,它表明脂肪分解抵抗(已知与肥胖和衰老有关)可能是一种应对慢性感染的生存计划。