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霉酚酸酯可减轻有症状颈动脉狭窄患者斑块炎症。

Mycophenolate mofetil attenuates plaque inflammation in patients with symptomatic carotid artery stenosis.

机构信息

Department of Vascular Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Atherosclerosis. 2010 Jul;211(1):231-6. doi: 10.1016/j.atherosclerosis.2010.01.043. Epub 2010 Feb 6.

Abstract

Atherosclerosis as well as the subsequent progression towards cardiovascular events are considered to, at least partially, be a consequence of chronic inflammatory activity. Therefore, we decided to evaluate the impact of short-term immunosuppressive treatment on plaque characteristics in patients with symptomatic carotid artery stenosis. Twenty-one patients were randomized to receive either 1000 mg. Mycophenolate mofetil (MMF) BD or placebo for at least 2 weeks prior to undergoing carotid endarterectomy (CEA). The serial sections of the CEA specimens were immunostained for activated T-cells (CD3+CD69+), regulatory T-cells (CD3+FOXP3+) and macrophages (CD68). In addition, gene expression profiling was performed by Illumina gene-array. Immunostaining revealed a reduction of activated T-cells in nine MMF-treated patients compared to 11 placebo-treated control patients (19.7% vs. 28.1%; p<0.05) as well as an increase of regulatory T-cells (3.8% vs. 1.8%; p=0.05). Microarray analyses confirmed beneficial changes to plaque phenotype, showing reduced expression of pro-inflammatory genes. Significantly reduced expression of metalloproteinases and osteopontin was observed in three out of nine MMF-treated patients compared to nil out of 11 in the placebo group. In the present study we show that immunosuppressive treatment for two-and-a-half weeks prior to CEA elicits changes in the plaque phenotype of symptomatic patients. These changes include reduced inflammatory cell presence with a concomitant decrease in pro-inflammatory gene expression.

摘要

动脉粥样硬化以及随后向心血管事件的进展被认为至少部分是慢性炎症活动的结果。因此,我们决定评估短期免疫抑制治疗对有症状颈动脉狭窄患者斑块特征的影响。21 名患者被随机分为两组,分别在接受颈动脉内膜切除术(CEA)前至少 2 周接受 1000mg 霉酚酸酯(MMF)BD 或安慰剂治疗。CEA 标本的连续切片用激活的 T 细胞(CD3+CD69+)、调节性 T 细胞(CD3+FOXP3+)和巨噬细胞(CD68)进行免疫染色。此外,还通过 Illumina 基因芯片进行基因表达谱分析。免疫染色显示,与 11 名安慰剂治疗的对照组患者相比,9 名 MMF 治疗患者的活化 T 细胞减少(19.7%对 28.1%;p<0.05),调节性 T 细胞增加(3.8%对 1.8%;p=0.05)。微阵列分析证实了斑块表型的有益变化,显示促炎基因表达减少。与安慰剂组 11 名患者中无一例相比,在 9 名 MMF 治疗患者中有 3 名患者观察到金属蛋白酶和骨桥蛋白的表达显著减少。在本研究中,我们表明 CEA 前两周半的免疫抑制治疗会引起有症状患者斑块表型的变化。这些变化包括炎症细胞存在减少,同时促炎基因表达减少。

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