Innate and Adaptive Immunity in Calcific Aortic Valve Disease

被引:93
|
作者
Mathieu, Patrick [1 ,2 ]
Bouchareb, Rihab [1 ,2 ]
Boulanger, Marie-Chloe [1 ,2 ]
机构
[1] Univ Laval, Res Ctr, Quebec Heart & Lung Inst, Dept Surg,LEMV,GRV, Quebec City, PQ G1K 7P4, Canada
[2] Inst Cardiol & Pneumol Quebec, Quebec City, PQ G1V 4G5, Canada
关键词
NF-KAPPA-B; TUMOR-NECROSIS-FACTOR; LOW-DENSITY-LIPOPROTEIN; VALVULAR INTERSTITIAL-CELLS; ELASTOLYTIC CATHEPSIN-S; TNF FAMILY-MEMBER; ANGIOTENSIN-II; FACTOR-ALPHA; T-LYMPHOCYTES; EARLY LESION;
D O I
10.1155/2015/851945
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Calcific aortic valve disease (CAVD) is the most common heart valve disorder. CAVD is a chronic process characterized by a pathologic mineralization of valve leaflets. Ectopic mineralization of the aortic valve involves complex relationships with immunity. Studies have highlighted that both innate and adaptive immunity play a role in the development of CAVD. In this regard, accumulating evidence indicates that fibrocalcific remodelling of the aortic valve is associated with activation of the NF-kappa B pathway. The expression of TNF-alpha and IL-6 is increased in human mineralized aortic valves and promotes an osteogenic program as well as the mineralization of valve interstitial cells (VICs), the main cellular component of the aortic valve. Different factors, including oxidized lipid species, activate the innate immune response through the Toll-like receptors. Moreover, VICs express 5-lipoxygenase and therefore produce leukotrienes, which may amplify the inflammatory response in the aortic valve. More recently, studies have emphasized that an adaptive immune response is triggered during CAVD. Herein, we are reviewing the link between the immune response and the development of CAVD and we have tried, whenever possible, to keep a translational approach.
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页数:11
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