Puxeddu Ilaria, Petrelli Fiorella, Angelotti Francesca, Croia Cristina, Migliorini Paola
Clinical Immunology Unit, Department of Clinical and Experimental Medicine, Pisa University, Pisa, Italy.
J Asthma Allergy. 2019 Sep 20;12:285-295. doi: 10.2147/JAA.S184986. eCollection 2019.
Chronic urticaria (CU) is a mast cell-driven disease characterized by the development of wheals, angioedema, or both for more than 6 weeks. The two major sub-types are chronic spontaneous urticaria (CSU) and inducible urticaria. In the last decade different pathophysiological mechanisms, potentially responsible for the development of the disease, have been described. It is likely that the activation of mast cells and basophils in CSU can be the results of immune system dysregulation, activation of the inflammatory cascade, and of the extrinsic coagulation pathway. Some of the mediators involved in the pathophysiological mechanisms of CSU have recently been identified as potential biomarkers useful for the diagnosis, follow-up, and management of the disease, even if they are not yet available in clinical practice. Thus, in this review we discuss new insights in the mediators involved in the pathogenesis of CSU, highlighting their potential role as biomarkers in the activity and progression of the disease and response to therapies.
慢性荨麻疹(CU)是一种由肥大细胞驱动的疾病,其特征为风团、血管性水肿或两者兼有的症状持续超过6周。两大主要亚型为慢性自发性荨麻疹(CSU)和诱导性荨麻疹。在过去十年中,已经描述了可能导致该疾病发生的不同病理生理机制。CSU中肥大细胞和嗜碱性粒细胞的激活可能是免疫系统失调、炎症级联反应激活以及外源性凝血途径激活的结果。最近,一些参与CSU病理生理机制的介质已被确定为对该疾病的诊断、随访和管理有用的潜在生物标志物,尽管它们尚未应用于临床实践。因此,在本综述中,我们讨论了CSU发病机制中涉及的介质的新见解,强调了它们作为生物标志物在疾病活动、进展及对治疗反应方面的潜在作用。