Regulatory T Cells and the Control of Modified Lipoprotein Autoimmunity-Driven Atherosclerosis

被引:47
作者
Nilsson, Jan [1 ]
Wigren, Maria [1 ]
Shah, Prediman K. [2 ,3 ,4 ]
机构
[1] Lund Univ, Malmo Univ Hosp, Dept Clin Sci, SE-20502 Malmo, Sweden
[2] Cedars Sinai Med Ctr, Atherosclerosis Res Ctr, Los Angeles, CA 90048 USA
[3] Cedars Sinai Med Ctr, Div Cardiol, Los Angeles, CA 90048 USA
[4] UCLA Sch Med, David Geffen Sch Med, Los Angeles, CA 90048 USA
关键词
LOW-DENSITY-LIPOPROTEIN; E-DEFICIENT MICE; E-KNOCKOUT MICE; APOLIPOPROTEIN-E; OXIDIZED LDL; PEPTIDE SEQUENCES; AGGRAVATES ATHEROSCLEROSIS; REDUCES ATHEROSCLEROSIS; NULL MICE; IMMUNIZATION;
D O I
10.1016/j.tcm.2010.02.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has long been recognized that arterial inflammation plays a key role in the development of atherosclerosis. More recent evidence has suggested that this inflammation is modulated by autoimmune responses against modified self-antigens, such as oxidized low-density lipoprotein, in the vascular wall. However, the role of the immune system in atherosclerosis appears to be more complex than in classic autoimmune diseases; and a number of protective immune responses have also been identified. One of the most important of these is carried out by the regulatory T cells. Regulatory T cells inhibit the development of autoimmunity by controlling the activity of autoreactive T cells. If the function of regulatory T cells is compromised in hypercholesterolemic mouse models of atherosclerosis, the development of disease becomes much more aggressive. In this review, we will discuss the possibility that the inflammatory activity in atherosclerotic lesions depends on the balance between plaque antigen-specific proinflammatory Th1-type T cells and anti-inflammatory regulatory T cells specific for the same antigen. We will also discuss the role of hypercholesterolemia in generation of these modified self-antigens as well as ongoing research aiming to develop novel immune-modulating therapy for prevention of cardiovascular disease by targeting these processes. (Trends Cardiovasc Med 2009;19:272-276) (C) 2009, Elsevier Inc.
引用
收藏
页码:272 / 276
页数:5
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