Wagner Nicola, Berking Carola
Hautklinik, Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054, Erlangen, Deutschland.
Hautklinik, Uniklinikum Erlangen, 91054, Erlangen, Germany.
Dermatologie (Heidelb). 2024 Apr;75(4):289-294. doi: 10.1007/s00105-024-05311-0. Epub 2024 Feb 27.
Various mechanisms contributing to the activity of chronic spontaneous urticaria (CU) have been postulated. Associated comorbidities are increasingly leading to the discovery of further signaling pathways which may support the activity of chronic urticaria or contribute to low-grade systemic inflammation. Moreover psychoimmunological factors may also be involved. The aim of this work is to improve the clinical care of patients with CU by increasing knowledge regarding optional influencing factors due to comorbidities and to possibly influence disease activity. Chronic urticaria due to autoimmune mechanisms may dispose to other autoimmune diseases, especially autoimmune thyroiditis, which can trigger chronic disease. Association of CU with metabolic syndrome has received little attention to date. Obesity may contribute to low-grade systemic inflammation by cytokine-secreting adipose tissue and hence to mediator-release of mast cells. Furthermore, neuroimmunological pathways, especially increased release of substance P, an activating ligand of Mas-related G protein-coupled receptor X2 (MRGPX2) on mast cells, should be addressed when optimizing therapy.
关于慢性自发性荨麻疹(CU)活动的各种机制已被提出。相关的合并症越来越多地促使人们发现更多的信号通路,这些通路可能支持慢性荨麻疹的活动或导致低度全身炎症。此外,心理免疫因素也可能参与其中。这项工作的目的是通过增加对合并症相关可选影响因素的了解来改善CU患者的临床护理,并可能影响疾病活动。自身免疫机制导致的慢性荨麻疹可能易患其他自身免疫性疾病,尤其是自身免疫性甲状腺炎,后者可引发慢性疾病。迄今为止,CU与代谢综合征的关联很少受到关注。肥胖可能通过分泌细胞因子的脂肪组织导致低度全身炎症,从而导致肥大细胞释放介质。此外,在优化治疗时,应考虑神经免疫途径,尤其是P物质(一种肥大细胞上Mas相关G蛋白偶联受体X2(MRGPX2)的激活配体)释放增加的情况。