Atorvastatin Modulates Th1/Th2 Response in Patients With Chronic Heart Failure

被引:70
作者
Cheng, Xiang [1 ]
Ding, Yingjun [1 ]
Xia, Chunyan [1 ]
Tang, Tingting [1 ]
Yu, Xian [1 ]
Xie, Jiangjiao [1 ]
Liao, Mengyang [1 ]
Yao, Rui [1 ]
Chen, Yong [1 ]
Wang, Min [1 ]
Liao, Yu-Hua [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Inst Cardiol, Lab Cardiovasc Immunol,Tongji Med Coll, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
Chronic heart failure; T lymphocyte; helper; HMG-CoA reductase inhibitor; T-CELLS; IMBALANCE; STATINS; ENCEPHALOMYELITIS; INFLAMMATION; ACTIVATION; PARALYSIS; PROMOTES; MARKERS;
D O I
10.1016/j.cardfail.2008.10.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
dBackground: The T-helper (Th)1/Th2 imbalance has been demonstrated to be involved in chronic heart failure (CHF). We sought to determine whether atorvastatin exhibited any effect on CHF through modulating the Th1/Th2 response. Methods and Results: We measured serum concentrations of interleukin(IL)-12, -18, interferon(IFN)-gamma, IL-4. and IL-10 from 20 controls and 72 patients with nonischemic CHF by enzyme-linked immunosorbent assay. To investigate the effect of atorvastatin in vivo, CHF patients were either classified into a Usual therapy group (n = 35) or usual therapy Plus atorvastatin ( 10 mg/day) group (it = 37). Patient serum levels of IFN-gamma and IL-4 were measured at time of admission and 2 weeks after treatment. Peripheral blood mononuclear cells from patients of CHF g-roup were Cultured in the presence or absence of atorvastatin (0, 0.4, 1, and 4 mu mol/L) in vitro, and IFN-gamma and IL-4 levels were detected. Serum levels of IL-12, IL-18, and IFN-gamma were significantly higher in the CHF group than in the control group. The levels of IFN-gamma and the ratios of IFN-gamma:IL-4 were significantly decreased with atorvastatin treatment both in vivo and in vitro, whereas levels of IL-4 did not differ significantly. Conclusions: Th1 polarization exists in patients with CHF. and atorvastatin can modulate the Th1/Th2 response through inhibiting Th I cytokine production. (J Cardiac Fail 2009;15:158-162)
引用
收藏
页码:158 / 162
页数:5
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