期刊文献+

强化他汀治疗对不稳定心绞痛患者自身免疫的影响 被引量:12

Impact of high-load atorvastatin on autoimmunity in patients with unstable angina
下载PDF
导出
摘要 目的探讨强化他汀治疗对行经皮冠状动脉介入术(PCI)术后不稳定心绞痛(UA)患者外周血T细胞亚群的影响。方法选择2012年9月至2013年4月在唐山市工人医院住院并行PCI术的UA患者180例分为高负荷量他汀治疗组、常规负荷量他汀治疗组、常规治疗组,每组60例。采用流式细胞分析法检测各组患者术前1d和术后1周、1个月、6个月外周血CD4+,CD8+细胞占T淋巴细胞比例,CD4+CD25+Treg细胞占CD4+T细胞比例。结果不同剂量的阿托伐他汀钙在术后1周、1个月、6个月均可降低CD4+T细胞比例,升高CD8+T细胞比例,同时升高CD4+CD25+Treg细胞占CD4+T细胞比例且服用时间越长效果越明显(P<0.05);高负荷量他汀治疗组在术后1个月、6个月外周血CD4+,CD8+细胞占T淋巴细胞比例和CD4+CD25+Treg细胞占CD4+T细胞比例与同时间点常规负荷量他汀治疗组和常规治疗组相比差异亦有统计学意义(P<0.05)。结论阿托伐他汀钙通过调节UA患者外周血T细胞亚群的平衡状态而降低UA的发病且强化他汀治疗后临床疗效更显著。 Objective To explore the impact of high-load atorvastatin on T cell subsets in patients with unstable angina (UA) after percutaneous coronary intervention (PCI) .Methods One hundred and eighty patients with UA were randomly divided into high-load atorvastatin group ,ordinary-load atorvastatin group and routine group ,60 cases in each group .The ratios of CD4^+ T cell , CD8^+ T cell and the frequencies of CD4^+ CD25^+ Treg were detected in 3 groups 1 day before PCI and 1 week ,1 month and 6 months after PCI by flow cytometry analysis .Results Different doses of atorvastatin reduced the ratio of CD4^+ T cells and increased the ratio of CD8^+ T cells and also the frequencies of CD4^+ CD25^+ Treg after PCI for 1 week ,1 month and 6 months .The longer the time to take atorvastatin ,the more obvious the effect was(P〈0 .05) .The ratios of CD4^+ ,CD8+ T cells and the frequencies of CD4^+CD25^+ Treg after PCI for 1 month and 6 months in high-load atorvastatin showed significant difference compared with those in ordinary-load atorvastatin group and routine group(P〈0 .05) .Conclusion Atorvastatin could regulate the balance of T cell subsets in patients with UA ,and thus it may reduce the UA onset and the treatment effect of high-load atorvastatin is more sig-nificant .
出处 《重庆医学》 CAS 北大核心 2015年第1期42-44,共3页 Chongqing medicine
基金 唐山市科技支撑计划项目(12150222B-15)
关键词 心绞痛 不稳定 T淋巴细胞 他汀 angina,unstable T-Lymphocytes atorvastatin
  • 相关文献

参考文献12

  • 1Moore KJ, Tabas I. Macrophages in the pathogenesis of atherosclerosis[J]. Cell, 2011,145 (3): 341. 被引量:1
  • 2Cretney E, Xin A, Shi W, et al. The transcription factors Blimp-1 and IRF4 jointly control the differentiation and function of effector regulatory T cells[J]. Nat Immunol, 2011,12(4) :304-311. 被引量:1
  • 3刘俊,李建军.动脉粥样硬化中的免疫调节[J].中国动脉硬化杂志,2011,19(11):957-962. 被引量:11
  • 4Keaney JF. Immune modulation of atherosclerosis[J]. Circulation,2011,124(22) :e559-560. 被引量:1
  • 5NNakamura K, Sasaki T, Cheng XW, et al. Statin prevents plaque disruption in apoE-knockout mouse model through pleiotropic effect on acute inflammation[J]. Atherosclero- sis,2009,206(2) :355-361. 被引量:1
  • 6Buja LM, Willerson JT. Role of inflammation in coronary plaque disruption[J]. Circulation, 1994,89(1) :503-505. 被引量:1
  • 7Neri Serneri GG, Prisco D, Martini F, et al. Acute T-cell activation is detectable in unstable angina[J]. Circulation, 1997,95(7): 1806-1812. 被引量:1
  • 8冯静,费瑜,孟晓萍.CD4^+和CD8^+ T淋巴细胞与动脉粥样硬化相关性研究进展[J].中国动脉硬化杂志,2011,19(8):707-710. 被引量:13
  • 9Sakaguchi S, Sakaguchi N, Asano M, et al. Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains(CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases[J]. J Immunol, 1995,155(3): 1151-1164. 被引量:1
  • 10Ait-Oufella H, Salomon BL, Potteaux S, et al. Natural regulatory T ceils control the development of atheroscle- rosis in mice[J]. Nat Med,2006,12(2)-178-180. 被引量:1

二级参考文献61

  • 1司敏,来庆友.C-反应蛋白与急性冠状动脉综合征[J].山东医药,2005,45(20):70-71. 被引量:3
  • 2杨欣,任卫东,马娜.动脉粥样硬化兔血管内皮功能与黏附分子VCAM-1表达关系的研究[J].中国现代医学杂志,2007,17(3):309-311. 被引量:9
  • 3Arcari CM, Gaydos CA, Nieto FJ, et al. Association be- tween chlamydia pneumoniae and acute myocardial infarc- tion in young men in the United States mihtary: the impor- tance of timing of exposure measurement [ J ~. Clim Infec Dis, 2005, 40(8) : 1 123-130. 被引量:1
  • 4George J, Shoenfeld Y, Harats D. The involvement of beta -2-g lyco protein -I(beta-2-GPI) in human and murine ath- erosclerosis [ J ]. J Autoimmun, 1999, 13 ( 1 ) : 57-60. 被引量:1
  • 5Zhou X, Nicoletti A, Elhage R, et al. Transfer of CIM + Tcells aggravates atherosclerosis in immunodeficient apoli- poprotein E knockout mice [ J ]. Circulation, 2000, 102 (24) : 2 919-922. 被引量:1
  • 6Lesley Mac, Donald-Wicks, Manohar Garg. Oxidized LDL and antioxidants in atherosclerosis biomedical and life sci- ences [ M]. Biochem Atheroscler, 2006, Section V: 519- 541. 被引量:1
  • 7Steffens SF, Burger GP. Short-term treatment with anti- CD3 antibody reduces the development and progression of atherosclerosis in mice [J]. Circulation, 2006, 114(3) : 1 977-984. 被引量:1
  • 8Skihon MR. Intrauterine risk factors for precocious athero- sclerosis [ J ]. Pediatrics, 2008, 121 (3) : 570-574. 被引量:1
  • 9Binder CJ, Shaw PX, Chang MK, et al. The role of natu- ral antibodies in atherogenesis [J]. Lipid Res, 2005, 46 (7) : 1 353-363. 被引量:1
  • 10Lopez LR, Kobayashi K, Matsunami Y, et al. Immuno- genic oxidized low-density lipoprotein/beta2-glycoprotein Icomplexes in the diagnostic management of atherosclero- sis. [J]. Clin Rev Allergy Immunol, 2009, 37(1) : 12- 19. 被引量:1

共引文献21

同被引文献122

引证文献12

二级引证文献83

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