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川崎病相关免疫炎症反应及血管内皮功能障碍的研究进展

Advances in understanding Kawasaki disease-related immuno-inflammatory response and vascular endothelial dysfunction.

作者信息

Wang Yuchen, Li Tao

机构信息

Department of Pediatrics, Affiliated Taihe Hospital of Hubei University of Medicine Shiyan Hubei China.

出版信息

Pediatr Investig. 2022 Aug 1;6(4):271-279. doi: 10.1002/ped4.12341. eCollection 2022 Dec.

Abstract

Kawasaki disease (KD) is a systemic vasculitis of unknown etiology, which tends to involve coronary arteries and can lead to acquired heart disease in children. The immuno-inflammatory response and vascular endothelial dysfunction are important causes of coronary artery disease in patients with KD. Multisystem inflammatory syndrome in children (MIS-C) is a rare inflammatory disease in children identified in recent years, which is caused by severe acute respiratory syndrome coronavirus 2 infection; this disease overlaps with KD. This review examines research progress concerning the immuno-inflammatory response and vascular endothelial dysfunction associated with KD, as well as differences between KD and MIS-C.

摘要

川崎病(KD)是一种病因不明的全身性血管炎,易累及冠状动脉,可导致儿童获得性心脏病。免疫炎症反应和血管内皮功能障碍是KD患者冠状动脉疾病的重要病因。儿童多系统炎症综合征(MIS-C)是近年来发现的一种罕见的儿童炎症性疾病,由严重急性呼吸综合征冠状病毒2感染引起;这种疾病与KD有重叠。本文综述了与KD相关的免疫炎症反应和血管内皮功能障碍的研究进展,以及KD与MIS-C之间的差异。

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