了解川崎病相关免疫炎症反应和血管内皮功能障碍的进展。

IF 1.9 4区 医学 Q2 PEDIATRICS Pediatric Investigation Pub Date : 2022-08-01 eCollection Date: 2022-12-01 DOI:10.1002/ped4.12341
Yuchen Wang, Tao Li
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引用次数: 0

摘要

川崎病(KD)是一种病因不明的全身性血管炎,往往累及冠状动脉,可导致儿童后天性心脏病。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原因。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,由严重急性呼吸系统综合征冠状病毒2感染引起;这种疾病与KD重叠。本综述探讨了与儿童多系统炎症综合征相关的免疫炎症反应和血管内皮功能障碍的研究进展,以及儿童多系统炎症综合征和儿童多系统炎症综合征之间的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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.

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来源期刊
Pediatric Investigation
Pediatric Investigation Medicine-Pediatrics, Perinatology and Child Health
CiteScore
3.30
自引率
0.00%
发文量
176
审稿时长
12 weeks
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