Furukawa S, Matsubara T, Motohashi T, Tsuda M, Sugimoto H, Yabuta K
Department of Pediatrics, Juntendo University School of Medicine, Tokyo, Japan.
Acta Paediatr Jpn. 1991 Dec;33(6):745-51. doi: 10.1111/j.1442-200x.1991.tb02603.x.
A review of our previous immunological studies on Kawasaki disease (KD) was undertaken. The results showed that peripheral blood macrophages/monocytes, T-cells and B-cells become activated during acute KD in terms of numerical changes in immunocompetent cells, expression of activated antigens on the cell surfaces and cytokine production. Also, during acute KD with coronary artery lesions (CALs) the numbers of macrophages/monocytes are increased. In addition, both the increased levels of tumor necrosis factor-alpha and shed intercellular adhesion molecule-1 in serum are more evident in KD patients with CALs than in those without. Our results further suggest that the main characteristics of the pathogenesis of KD are increased numbers of peripheral blood macrophages/monocytes with the secretion of monokines by these activated cells, and the expression of adhesion molecules on immunocompetent cells. These immune responses develop more vigorously in KD patients with CALs.
我们对之前关于川崎病(KD)的免疫学研究进行了回顾。结果显示,在急性KD期间,外周血巨噬细胞/单核细胞、T细胞和B细胞在免疫活性细胞数量变化、细胞表面活化抗原表达以及细胞因子产生方面均被激活。此外,在伴有冠状动脉病变(CALs)的急性KD期间,巨噬细胞/单核细胞数量增加。另外,血清中肿瘤坏死因子-α和可溶性细胞间黏附分子-1水平升高在伴有CALs的KD患者中比无CALs的患者更为明显。我们的结果进一步表明,KD发病机制的主要特征是外周血巨噬细胞/单核细胞数量增加,这些活化细胞分泌单核因子,以及免疫活性细胞上黏附分子的表达。这些免疫反应在伴有CALs的KD患者中更为强烈。