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摘要: 目的:探讨趋化因子CCL21及其受体CCR7与冠状动脉(冠脉)易损斑块之间的关系。方法:选择行冠脉造影(CAG)患者180例,其中急性冠脉综合征(ACS)患者60例(ACS组),稳定型心绞痛(SAP)患者60例(SAP组),CAG正常且没有其他粥样硬化证据患者60例(对照组)。ACS组和SAP组患者在CAG后行血管内超声(IVUS)检查。采用双抗体夹心酶联免疫吸附法(ELISA法)检测血清趋化因子CCL21及高敏C反应蛋白(hs-CRP)的浓度,用流式细胞术测定外周淋巴细胞表面CCR7的表达水平。结果:血清趋化因子CCL21浓度与外周淋巴细胞CCR7的表达在各组之间有显著差异(均P<0.05);应用CCL21判断ACS的ROC曲线下面积,大于应用hs-CRP判断ACS的ROC曲线下面积[(0.803±0.027)︰(0.716±0.021),P<0.01]。IVUS发现ACS组主要为脂质性斑块(65%),而SAP组主要为纤维性斑块(57%),脂质斑块仅占13%,两组差异有统计学意义(P<0.01);ACS组斑块负荷和血管重构指数明显大于SAP组(P<0.01);利用IVUS测定的斑块负荷与趋化因子CCL21浓度呈显著正相关(r=0.795,P<0.01),与外周淋巴细胞表面CCR7的表达呈显著负相关(r=-0.693,P<0.01)。结论:趋化因子CCL21及其受体CCR7与冠脉斑块易损性密切相关,较hs-CRP具有更高的早期诊断和判断预后的价值。Abstract: Objective: To investigate the relationship between the chemotactic factor CCL21 and its receptor CCR7 and coronary vulnerable plaque. Method: A total of 180 patients underwent coronary angiography (CAG) was included into three groups:acute coronary syndrome (ACS) group (n=60), stable angina pectoris (SAP) group (n=60) and control group (patients with normal coronary angiography and without other evidence of atherosclerosis, n=60). ACS group and SAP group underwent intravascular ultrasound (IVUS) examination after CAG.Double antibody sandwich enzyme linked immunosorbent assay (ELISA method) was used to detect the serum levels of chemokine CCL21 and hs-CRP, flow cytometry was used to determin the expression of peripheral CCR7. Result: Serum levels of chemokine CCL21 concentration and expression of peripheral lymphocyte CCR7 had significant difference in three groups (all P<0.05). The area under the ROC curve of CCL21 was greater than that of hs-CRP[(0.803±0.027)︰(0.716±0.021), P<0.01]. IVUS results showed that ACS group mainly had lipid plaque (65%), and SAP group mainly had fibrous plaque (57%)accompanied by only13%lipid plaque (P<0.01). The plaque load and vascular remodeling index in ACS group were significantly higher than those in SAP group (both P<0.01). The plaque load was significantly positively correlated with chemokine CCL21 concentration (r=0.795, P<0.01), and significantly negatively correlated with the expression of peripheral lymphocyte surface CCR7 (r=-0.693, P<0.01). Conclusion: Chemokine CCL21 and its receptor CCR7 are closely related to coronary plaque vulnerability, and have more early diagnosis and prognosis values than hs-CRP.
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Key words:
- coronary heart disease /
- chemokme /
- vulnerable plaque /
- mtravascular ultrasound
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[1] MATHERS C D,LONCAR D.Projections of global mortality and burden of disease from 2002to 2030[J].PLoS Med,2006,3:e442.
[2] WEBER C,NOELS H.Atherosclerosis:Current pathogenesis and therapeutic options[J].Nat Med,2011,17:1410-1422.
[3] DAMS J K,SMITH C,IE E,et al.Enhanced expression of the homeostatic chemokines CCL19 and CCL21 in clinical and experimental atherosclerosis:possible pathogenic role in plaque destabilization[J].Arterioscler Thromb Vasc Biol,2007,27:614-620.
[4] KOENEN R R,WEBER C.Chemokines:Established and novel targets in atherosclerosis[J].EMBO Mol Med,2011,3:713-725.
[5] ZUO H,LIU Q,ZHANG Z,et al.Outcomes of percutaneous coronary intervention for intermediate coronary artery disease guided by intravascular ultrasound or fractional flow reserve[J].J South Med Univ,2014,34:704-708.
[6] JIN T,XU X,HERELD D.Chemotaxis,chemokine receptors and human disease[J].Cytokine,2008,44:1-8.
[7] LUCHTEFELD M,GROTHUSEN C,GAGALICK A,et al.Chemokine receptor 7knock out attenuates atherosclerotic plaque development[J].Circulation,2010,122:1621-1628.
[8] FORSTER R,DAVALOS-MISSLITZ A C,ROT A.Ccr7 and its ligands:Balancing immunity and tolerance[J].Nat Rev Immunol,2008,8:362-371.
[9] FEVANG B,YNDESTAD A,DAMAS J K,et al.Chemokines andcommon variable immunodeficiency;possible contribution of CCL19,CCL21 and CCR7 to immune dysregulation[J].Clin Exp Immunol,2009,158:237-245.
[10] DAMS J K,SMITH C,IE E,et al.Enhanced expression of the homeostatic chemokines CCL19 and CCL21 in clinical and experimental atherosclerosis[J].Arterioscler Thromb Vasc Biol,2007,27:614-620.
[11] PONDA M P,BARASH I,FEIG J E,et al.Moderate kidney disease inhibits atherosclerosis regression[J].Atherosclerosis,2010,210:57-62.
[12] FEIG J E,RONG J X,SHAMIR R,et al.HDL promotes rapid atherosclerosis regression in mice and alters inflammatory properties of plaque monocyte-derived cells[J].Proc Natl Acad Sci U S A,2011,108:7166-7171.
[13] NICKEL T,PFEILER S,SUMMO C,et al.oxLDL downregulates the dendritic cell homing factors CCR7 and CCL21[J].Mediators Inflamm,2012,2012:320953.
[14] HONG M K,MINTZ G S,LEE C W,et al.A Three-vessel virtual histology intravascular ultrasound analysis of frequency and distribution of thin-cap fibroatheromas in patients with acute coronary syndrome or stable angina pectoris[J].Am J Cardiol,2008,101:568-572.
[15] IVANOVIC M,RANCIC M,RDZANEK A,et al.Virtual histology study of atherosclerotic plaque composition in patients with stable angina and acute phase of acute coronary syndromes without ST segment elevation[J].Srp Arh Celok Lek,2013,141:308-314.
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