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急性川崎病期间外周血单核细胞/巨噬细胞和T细胞中的核因子κB激活

NF-kappaB activation in peripheral blood monocytes/macrophages and T cells during acute Kawasaki disease.

作者信息

Ichiyama T, Yoshitomi T, Nishikawa M, Fujiwara M, Matsubara T, Hayashi T, Furukawa S

机构信息

Department of Pediatrics, Yamaguchi University School of Medicine, 1-1-1 Minamikogushi, Ube, Yamaguchi, 755-8505, Japan.

出版信息

Clin Immunol. 2001 Jun;99(3):373-7. doi: 10.1006/clim.2001.5026.

Abstract

Kawasaki disease (KD) is a febrile disease of childhood characterized by systemic vasculitis, and the levels of many proinflammatory cytokines are elevated in the serum at the acute stage. We investigated the activation of transcription factor NF-kappaB for genes that encode the proinflammatory cytokines in CD14+ monocytes/macrophages and CD3+ T cells in peripheral blood by means of Western blot and flow cytometric analyses. Western blot analysis demonstrated that NF-kappaB activation was more increased in CD14+ monocytes/macrophages than in CD3+ T cells in all children during the acute stage. Flow cytometric analysis revealed that NF-kappaB activation in CD14+ monocytes/macrophages was significantly higher than in CD3+ T cells at the acute stage (30.0 +/- 16.0% vs 11.4 +/- 5.0%, P < 0.01, Wilcoxon test). NF-kappaB activation in CD14+ monocytes/macrophages was significantly decreased after high-dose intravenous immunoglobulin therapy (P < 0.05). The present findings suggest that CD14+ monocytes/macrophages play an important role in cytokine production during acute KD.

摘要

川崎病(KD)是一种以全身性血管炎为特征的儿童发热性疾病,急性期血清中多种促炎细胞因子水平升高。我们通过蛋白质印迹法和流式细胞术分析,研究了外周血中CD14 +单核细胞/巨噬细胞和CD3 + T细胞中编码促炎细胞因子的基因的转录因子NF-κB的激活情况。蛋白质印迹分析表明,急性期所有儿童中,CD14 +单核细胞/巨噬细胞中的NF-κB激活比CD3 + T细胞中增加得更多。流式细胞术分析显示,急性期CD14 +单核细胞/巨噬细胞中的NF-κB激活明显高于CD3 + T细胞(30.0±16.0%对11.4±5.0%,P<0.01,Wilcoxon检验)。大剂量静脉注射免疫球蛋白治疗后,CD14 +单核细胞/巨噬细胞中的NF-κB激活明显降低(P<0.05)。目前的研究结果表明,CD14 +单核细胞/巨噬细胞在急性KD期间的细胞因子产生中起重要作用。

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