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Rationale and study design for a phase I/IIa trial of anakinra in children with Kawasaki disease and early coronary artery abnormalities (The ANAKID Trial)

机译:川崎病和早期冠状动脉异常儿童的anakinra I / IIa期临床试验的理论基础和研究设计(ANAKID试验)

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摘要

BackgroundAlthough Kawasaki disease (KD) is the most common cause of acquired heart disease in children and may result in coronary artery aneurysms (CAA) with an attendant risk of myocardial infarction, there is no recommended therapy to halt progression of arterial wall damage and prevent aneurysm formation in the acute phase of the vasculitis. While intravenous immunoglobulin (IVIG) reduces the risk of CAA, up to 20% of KD patients are IVIG resistant and have a higher risk for developing CAA. The IL-1 pro-inflammatory pathway is upregulated in children with acute KD and plays a critical role in the experimental animal model of KD. Thus, IL-1 is a logical therapeutic target.
机译:背景尽管川崎病(KD)是儿童后天性心脏病的最常见病因,并可能导致冠状动脉瘤(CAA)并伴有心肌梗塞的风险,但没有建议的治疗方法可以阻止动脉壁损伤的进展并预防动脉瘤在血管炎的急性期形成。尽管静脉内免疫球蛋白(IVIG)降低了CAA的风险,但高达20%的KD患者对IVIG有抗药性,并且罹患CAA的风险更高。 IL-1促炎途径在急性KD儿童中上调,在KD实验动物模型中起关键作用。因此,IL-1是合乎逻辑的治疗靶标。

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