Matsubara T, Ichiyama T, Furukawa S
Department of Paediatrics, Yamaguchi University School of Medicine, Yamaguchi, Japan.
Clin Exp Immunol. 2005 Sep;141(3):381-7. doi: 10.1111/j.1365-2249.2005.02821.x.
Kawasaki disease (KD) is an acute illness of early childhood characterized by prolonged fever, diffuse mucosal inflammation, indurative oedema of the hands and feet, a polymorphous skin rash and nonsuppurative lymphadenopathy. The histopathological findings in KD comprise panvasculitis with endothelial necrosis, and the infiltration of mononuclear cells into small and medium-sized blood vessels. The levels of many proinflammatory cytokines, chemokines and adhesion molecules can be elevated in sera from children with KD at the acute stage. Although many immunological studies on KD involving peripheral blood have been reported, the data obtained remain controversial. This review focuses on the immune response of peripheral blood lymphocytes and monocytes/macrophages during acute KD.
川崎病(KD)是一种幼儿期急性疾病,其特征为持续发热、弥漫性黏膜炎症、手足硬性水肿、多形性皮疹和非化脓性淋巴结病。KD的组织病理学表现包括伴有内皮细胞坏死的全血管炎,以及单核细胞浸润至中小血管。急性期KD患儿血清中多种促炎细胞因子、趋化因子和黏附分子水平可能升高。尽管已经报道了许多关于KD外周血的免疫学研究,但所获得的数据仍存在争议。本综述重点关注急性KD期间外周血淋巴细胞和单核细胞/巨噬细胞的免疫反应。