期刊文献+

冠心病患者血清可溶性Fas和TNF-α水平变化 被引量:7

The change of serum concentration of soluble Fas and TNF-α in patients with coronary heart disease
下载PDF
导出
摘要 目的探讨血清可溶性Fas(sFas)和TNF-α水平与冠心病(CHD)之间的关系。方法采用酶联免疫吸附双抗体夹心ABC-ELISA方法测定57例CHD患者(CHD组)和23例对照组受试者血清sFas和TNF-α水平。结果CHD患者血清sFas水平高于对照组(P<0.01),TNF-α水平也高于对照组(P<0.05),且CHD患者血清sFas水平与TNF-α成正相关(r=0.289,P=0.029)。CHD患者中sFas水平不稳定型心绞痛(UA组)患者和急性心肌梗死(AMI组)患者高于稳定型心绞痛(SA组)患者(P<0.05)。结论高水平的血清sFas和TNF-α与CHD有关,可能通过细胞凋亡和炎症反应途径参与冠状动脉粥样硬化斑块的发生发展。 Objective To investigate the relationship between serum levels of soluble Fas (sFas) ,tumor necrosis factor-α (TNF-α)and coronary heart disease (CHD). Methods Enzyme-linked immunosorbent assay (ELISA) was used to measure the levels of sFas and TNF-α in the sera from 57 patients with CHD and 23 subjects without CHD as controls . Results Significant increases in the concentrations of sFas and TNF-α( P〈0.01 and P〈0.05 , respectively) were found in the serum from patients with CHD compared to the control group. Moreover, sFas and TNF-α were positively correlated in patients with CHD (r= 0.289,P=0.029 ). The serum level of sFas in patients with AMI or UA were higher than that in patients with SA (P〈0.05). Conclusion High levels of sFas and TNF-α have relationship with CHD. They may be contribute to the development of atherosclerotic plaque by cell apoptosis and inflammatory response.
出处 《中国心血管病研究》 CAS 2006年第2期133-135,共3页 Chinese Journal of Cardiovascular Research
关键词 抗原 CD95 肿瘤坏死因子Α 冠状动脉疾病 细胞凋亡 Antigen, CD95 Tumor necrosis factor α Coronary disease Apoptosis
  • 相关文献

参考文献10

  • 1[1]Hansson GK.Immune mechanisms in atherosclerosis.Artherioscler Thromb Vasc Biol,2001,21:1876-1890.
  • 2[2]Stoneman VEA,Bennett MR.Role of apoptosis in atherosclerosis and its therapeutic implications.Clin Sci,2004,107:343-354.
  • 3[3]Frostegard J,Ulfgren AK,Nyberg P,et al.Cytokine expression in advanced human atherosclerotic plaques:dominance of pro-inflammatory (Th1) and macrophage stimulating cytokines.Atherosclerosis,1999,145:33-45.
  • 4[4]Bennett MR.Apoptosis in the cardiovascular system.Heart,2002,87:480-487.
  • 5[5]Jeremias I,Kupatt C,Martin Villalba A,et al.Involvement of CD95/Apo-1/Fas in cell death after myocardial ischemia.Circulation,2000,102:915-920.
  • 6[6]Elahi AW,Vijayakumar AN,Lichstein E,et al.Interplay of antibody and T cell response in acute myocardial infarction.J Lab Clin Med,2001,138:112-118.
  • 7[7]Rubin LA,Nelson DL.The soluble interleukin-2 receptor:Biology,function,and clinical application.Ann Intern Med,1990,113:619-627.
  • 8葛长江,胡申江,郑霞,武垚森,陈治奎.不稳定型心绞痛病人血清sFas、sFasL及sIL-2R水平的临床价值[J].免疫学杂志,2003,19(1):50-52. 被引量:2
  • 9[9]Boyle JJ,Bowyer DE,Weissberg PL,et al.Human bloodderived macrophage induce apoptosis in human plaque-derived vascular smooth muscle cells by Fas-Ligand/Fas interactions.Arterioscler Thromb Vasc Biol,2001,21:1402-1407.
  • 10[10]Ankersmit HJ,Weber T,Auer J,et al.Increased serum concentrations of soluble CD95/Fas and caspase 1/ICE in patients with acute angina.Heart,2004,90:151-154.

二级参考文献2

共引文献1

同被引文献91

引证文献7

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部