Frequency of naturally-occurring regulatory T cells is reduced in patients with ST-segment elevation myocardial infarction

被引:44
作者
Sardella, Gennaro
De Luca, Leonardo
Francavilla, Vittorio
Accapezzato, Daniele
Mancone, Massimo
Sirinian, Maria Isabella
Fedele, Francesco
Paroli, Marino
机构
[1] Ist Super Sanita, Policlin Umberto I, Dept Cardiovasc & Resp Sci, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, European Hosp, Div Cardiol, Rome, Italy
[3] Univ Roma La Sapienza, Dept Internal Med, Rome, Italy
[4] Univ Roma La Sapienza, Dept Clin Med & Therapy, Rome, Italy
关键词
D O I
10.1016/j.thromres.2006.12.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Naturally-occurring regulatory T cells (Treg) constitute a mature T cell population characterized phenotypically by co-expression of CD4 and CD25(high) surface molecules. We investigated here the frequency of circulating Treg in patients presenting with STEMI in comparison with subjects without coronary artery disease (CAD). The effect of primary percutaneous coronary intervention (PCI) with implantation of a bare (BS) or paclitaxel-eluting stent (PES) on peripheral Treg distribution was also examined. Methods: Peripheral blood mononuclear cells were isolated from 30 consecutive patients presenting with STEMI and from 30 age-matched control subjects with angiographically normal coronary arteries. Treg were detected by flow cytometry according to their characteristic CD4(+)CD25(high) membrane phenotype, and their frequency was assessed before PCI and at 48 h and at 6 days after PCI. CD27 expression identifying a highly suppressive Treg subset was also analysed. Results: The percentages of both (CD27+)Treg and (CD27-)Treg were significantly lower in patients with STEMI in comparison with controls. In addition, the c (CD27+)Treg/(CD27-)Treg ratio was skewed toward the CD27(-) population. The frequency of both Treg subsets significantly increased 48h after either BS or PES implantation, remaining elevated for up to at least 6 days after PCI. Conclusions: Our data suggest that the percentage of circulating Treg is significantly reduced in patients with STEMI, suggesting that this immunosuppressive T-cell subset is compartmentalized within the acutely ischemic myocardium to limit the ongoing inflammation associated with this condition, and that coronary revascularization is associated with partial reconstitution of peripheral Treg pool. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:631 / 634
页数:4
相关论文
共 15 条
[1]   Natural regulatory T cells control the development of atherosclerosis in mice [J].
Ait-Oufella, H ;
Salomon, BL ;
Potteaux, S ;
Robertson, AKL ;
Gourdy, P ;
Zoll, J ;
Merval, R ;
Esposito, B ;
Cohen, JL ;
Fisson, S ;
Flavell, RA ;
Hansson, GK ;
Klatzmann, D ;
Tedgui, A ;
Mallat, Z .
NATURE MEDICINE, 2006, 12 (02) :178-180
[2]   CD4+ regulatory T cells:: Mechanisms of induction and effector function [J].
Bacchetta, R ;
Gregori, S ;
Roncarolo, MG .
AUTOIMMUNITY REVIEWS, 2005, 4 (08) :491-496
[3]   CD4+CD25high regulatory cells in human peripheral blood [J].
Baecher-Allan, C ;
Brown, JA ;
Freeman, GJ ;
Hafler, DA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1245-1253
[4]  
Bhan V, 2004, ONCOL REP, V11, P893
[5]   Increased Th1 activity in patients with coronary artery disease [J].
Fernandes, JL ;
Mamoni, RL ;
Orford, JL ;
Garcia, C ;
Selwyn, AP ;
Coelho, OR ;
Blotta, MHSL .
CYTOKINE, 2004, 26 (03) :131-137
[6]   The inflammatory response in myocardial infarction [J].
Frangogiannis, NG ;
Smith, CW ;
Entman, ML .
CARDIOVASCULAR RESEARCH, 2002, 53 (01) :31-47
[7]   Chemokine CXCL10 promotes atherogenesis by modulating the local balance of effector and regulatory T cells [J].
Heller, Eric A. ;
Liu, Emerson ;
Tager, Andrew M. ;
Yuan, Qian ;
Lin, Alexander Y. ;
Ahluwalia, Neil ;
Jones, Krister ;
Koehn, Stephanie L. ;
Lok, Vincent M. ;
Aikawa, Elena ;
Moore, Kathryn J. ;
Luster, Andrew D. ;
Gerszten, Robert E. .
CIRCULATION, 2006, 113 (19) :2301-2312
[8]  
HINTZEN RQ, 1993, J IMMUNOL, V151, P2426
[9]   CD27/CFSE-based ex vivo selection of highly suppressive alloantigen-specific human regulatory T cells [J].
Koenen, HJPM ;
Fasse, E ;
Joosten, I .
JOURNAL OF IMMUNOLOGY, 2005, 174 (12) :7573-7583
[10]   Enhanced T-helper-1 lymphocyte activation patterns in acute coronary syndromes [J].
Methe, H ;
Brunner, S ;
Wiegand, D ;
Nabauer, M ;
Koglin, J ;
Edelman, ER .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 45 (12) :1939-1945