The problem of accelerated atherosclerosis in systemic lupus erythematosus: Insights into a complex co-morbidity

被引:24
作者
Wade, Nekeithia S. [1 ]
Major, Amy S. [1 ,2 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pathol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Div Cardiovasc Med, Dept Med, Nashville, TN 37232 USA
关键词
Systemic lupus erythematosus; atherosclerosis; autoimmunity; cardiovascular disease; HIGH-DENSITY-LIPOPROTEIN; REGULATORY T-CELLS; DEFICIENCY INCREASES ATHEROSCLEROSIS; I INTERFERON SYSTEM; MURINE LUPUS; B-CELLS; RISK-FACTORS; ANTICARDIOLIPIN ANTIBODIES; THERAPEUTIC TARGETS; AUTOIMMUNE-DISEASE;
D O I
10.1160/TH11-05-0330
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatic autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus (SLE), are associated with antibodies to "self" antigens. Persons with autoimmune diseases, most notably SLE, are at increased risk for developing accelerated cardiovascular disease. The link between immune and inflammatory responses in the pathogenesis of cardiovascular disease has been firmly established; yet, despite our increasing knowledge, accelerated atherosclerosis continues to be a significant co-morbidity and cause of mortality in SLE. Recent animal models have been generated in order to identify mechanism(s) behind SLE-accelerated atherosclerosis. In addition, clinical studies have been designed to examine potential treatments options. This review will highlight data from recent studies of immunity in SLE and atherosclerosis and discuss the potential implications of these investigations.
引用
收藏
页码:849 / 857
页数:9
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