Pongratz Georg, Straub Rainer H
Abteilung für Rheumatologie und klinische Immunologie der Klinik für Gastroenterologie und interventionelle Endoskopie, Krankenhaus Barmherzige Brüder Regensburg, Prüfeninger Str. 86, 93049, Regensburg, Deutschland.
Medizinische Fakultät, der Universität Regensburg, Regensburg, Deutschland.
Z Rheumatol. 2023 Aug;82(6):451-461. doi: 10.1007/s00393-023-01387-6. Epub 2023 Jul 24.
In this review article the current model of the interaction between the sympathetic nervous system (SNS) and the immune system in the context of chronic inflammation is presented. Mechanisms in the interaction between the SNS and the immune system are shown, which are similar for all disease entities: 1) the biphasic effect of the sympathetic system on the inflammatory response with a proinflammatory, stimulating effect before and during the activation of the immune system (early) and a more inhibitory effect in late phases of immune activation (chronic). 2) The interruption of communication between immune cells and the brain by withdrawal of sympathetic nerve fibers from areas of inflammation, such as the spleen, lymph nodes or peripheral foci of inflammation. 3) The local replacement of catecholamines by neurotransmitter-producing cells to fine-tune the local immune response independently of the brain. 4) Increased activity of the SNS due to an imbalance of the autonomic nervous system at the systemic level, which provides an explanation for known disease sequelae and comorbidities due to the long duration of chronic inflammatory reactions, such as increased cardiovascular risk with hypertension, diabetes mellitus and catabolic metabolism. The understanding of neuroimmune interactions can lead to new therapeutic approaches, e.g., a stimulation of beta-adrenergic and even more an inhibition of alpha-adrenergic receptors or a restoration of the autonomic balance in the context of arthritis ) can make an anti-inflammatory contribution (more influence of the vagus nerve); however, in order to translate the theoretical findings into clinical action that is beneficial for the patient, controlled interventional studies are required.
在这篇综述文章中,介绍了慢性炎症背景下交感神经系统(SNS)与免疫系统相互作用的当前模型。展示了SNS与免疫系统相互作用的机制,这些机制在所有疾病实体中都是相似的:1)交感系统对炎症反应的双相作用,在免疫系统激活之前和期间(早期)具有促炎、刺激作用,而在免疫激活的后期(慢性期)具有更强的抑制作用。2)通过从炎症区域(如脾脏、淋巴结或外周炎症灶)撤回交感神经纤维,中断免疫细胞与大脑之间的通信。3)神经递质产生细胞对儿茶酚胺的局部替代,以独立于大脑微调局部免疫反应。4)由于全身水平自主神经系统失衡导致SNS活性增加,这为慢性炎症反应持续时间较长所导致的已知疾病后遗症和合并症提供了解释,如高血压、糖尿病和分解代谢增加带来的心血管风险增加。对神经免疫相互作用的理解可带来新的治疗方法,例如,刺激β-肾上腺素能受体,甚至更多地抑制α-肾上腺素能受体,或在关节炎背景下恢复自主平衡,可起到抗炎作用(迷走神经的影响更大);然而,为了将理论发现转化为对患者有益的临床行动,需要进行对照干预研究。