Rowley A H, Shulman S T, Mask C A, Finn L S, Terai M, Baker S C, Galliani C A, Takahashi K, Naoe S, Kalelkar M B, Crawford S E
Ward 12-140, Pediatrics W-140, Northwestern University Medical School, Chicago, IL 60611-3008, USA.
J Infect Dis. 2000 Oct;182(4):1183-91. doi: 10.1086/315832. Epub 2000 Sep 8.
The etiology and pathogenesis of Kawasaki disease (KD) remain unknown. As previously reported, in US patients with acute KD, IgA plasma cells (PCs) infiltrate the vascular wall. To determine whether IgA PCs are increased at mucosal sites in KD and to determine whether other nonvascular KD tissues are infiltrated by IgA PCs, the cells were immunolocalized and quantitated in tissue sections taken from 18 US and Japanese patients who died of acute KD and from 10 age-matched controls. IgA PCs were significantly increased in the trachea of patients who died of acute KD, compared with controls (P<.01), a finding that was similar to findings in children with fatal respiratory viral infection. IgA PCs also infiltrated coronary artery, pancreas, and kidney in all KD patients. These findings strongly support entry of the KD etiologic agent through the upper respiratory tract, resulting in an IgA immune response, with systemic spread to vascular tissue, pancreas, and kidney.
川崎病(KD)的病因和发病机制尚不清楚。如先前报道,在美国急性KD患者中,IgA浆细胞(PCs)浸润血管壁。为了确定KD患者黏膜部位的IgA PCs是否增加,以及其他非血管性KD组织是否被IgA PCs浸润,对18例死于急性KD的美国和日本患者以及10例年龄匹配的对照者的组织切片中的细胞进行了免疫定位和定量分析。与对照组相比,死于急性KD患者的气管中IgA PCs显著增加(P<0.01),这一发现与致命性呼吸道病毒感染儿童的发现相似。所有KD患者的冠状动脉、胰腺和肾脏中也有IgA PCs浸润。这些发现有力地支持了KD病原体通过上呼吸道进入,引发IgA免疫反应,并全身扩散至血管组织、胰腺和肾脏。