Okada Seigo, Hashimoto Shintaro, Miyake Akiko, Okada Yusuke, Hirano Reiji, Fukunaga Shinnosuke, Ishikawa Yuichi
Department of Pediatrics, Saiseikai Shimonoseki General Hospital, Yamaguchi, Japan.
Department of Pediatrics, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
Front Pediatr. 2020 Jan 28;8:6. doi: 10.3389/fped.2020.00006. eCollection 2020.
Although an etiology of Kawasaki disease (KD) is unknown, an aberrant innate immune system in predisposed individuals has been proposed to play a key role in the development of KD vasculitis. Various etiological pathogens have been proposed as the trigger of KD and a scaled injury preceding symptom onset has been reported as one of them. Here, we report a 17-month-old Japanese female who was hospitalized due to high fever lasting for 4 days with infection ruled out as a cause. On admission, she displayed severe sunburn all over her body following a prolonged period of outdoor play 5 days ago. On the 5 day of illness, she developed complete KD. Serum levels of high mobility group box 1, a representative for damage-associated molecular patterns (DAMPs), were elevated during acute phase and continued to decrease during subacute phase. This unique course suggested the inflammatory process of KD involving innate immunity via DAMPs.
虽然川崎病(KD)的病因尚不清楚,但有观点认为,易感个体的先天性免疫系统异常在KD血管炎的发展中起关键作用。多种病原体被认为是KD的触发因素,其中有报道称症状出现前的规模性损伤是触发因素之一。在此,我们报告一名17个月大的日本女性,因持续4天的高烧入院,排除感染因素。入院时,她在5天前长时间户外玩耍后全身出现严重晒伤。在患病第5天,她发展为完全型KD。血清中高迁移率族蛋白B1(一种损伤相关分子模式(DAMPs)的代表物)水平在急性期升高,并在亚急性期持续下降。这一独特病程提示KD的炎症过程涉及通过DAMPs的先天性免疫。