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Predisposing factors, pathogenesis and therapeutic intervention of Kawasaki disease

机译:川崎病的诱因,发病机制和治疗干预

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Kawasaki disease (KD) is an acute febrile childhood inflammatory disease, associated with coronary artery abnormalities. The disease is believed to result from an aberrant inflammatory response to an infectious trigger in a genetically predisposed individual. KD is associated with an endothelial cell injury as a consequence of T cell activation and cytotoxic effects of various proinflammatory cytokines. Intravenous immunoglobulin (IVIG) infusion and aspirin are the standard treatment of acute KD. However, 10-20% of patients show resistance to IVIG therapy and present higher risk of coronary vasculitis. The relative roles of second WIG infusion, corticosteroids, calcineurin inhibitors, interleukin-1 antagonists and anti-tumor necrosis factor agents remain uncertain. In this review, we highlight the predisposing factors, pathogenesis and therapeutic intervention of KD, particularly new therapeutics for IVIG-resistant patients.
机译:川崎病(KD)是一种急性发热性儿童炎性疾病,与冠状动脉异常有关。据信该疾病是由于遗传易感个体对感染触发的异常炎症反应所致。由于T细胞活化和各种促炎细胞因子的细胞毒性作用,KD与内皮细胞损伤有关。静脉注射免疫球蛋白(IVIG)和阿司匹林是急性KD的标准治疗方法。但是,有10-20%的患者表现出对IVIG治疗的抗药性,并表现出更高的冠状血管炎风险。二次WIG输注,皮质类固醇,钙调神经磷酸酶抑制剂,白介素-1拮抗剂和抗肿瘤坏死因子药物的相对作用仍不确定。在这篇综述中,我们重点介绍了KD的诱因,发病机理和治疗干预,尤其是针对IVIG耐药患者的新疗法。

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