Lymphocytic tumor necrosis factor receptor superfamily co-stimulatory molecules in the pathogenesis of atherosclerosis

被引:16
作者
Smeets, Esther [1 ]
Meiler, Svenja [1 ]
Lutgens, Esther [1 ,2 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Biochem, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Munich, Inst Cardiovasc Prevent IPEK, Munich, Germany
关键词
adaptive immune system; atherosclerosis; co-stimulatory molecules; lymphocytes; tumor necrosis factor receptor superfamily; REGULATORY T-CELLS; NF-KAPPA-B; CD40; LIGAND; OX40; ACTIVATION; ATHEROGENESIS; PATHWAY; MICE; INFLAMMATION; DEPLETION;
D O I
10.1097/MOL.0000000000000025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose of reviewThe role of lymphocytes in the chronic inflammatory disease atherosclerosis has emerged over the past decade. Co-stimulatory molecules of the heterogeneous tumor necrosis factor receptor superfamily play a pivotal role in lymphocyte activation, proliferation and differentiation. Here we describe the immune modulatory properties and mechanisms of four tumor necrosis factor receptor superfamily members in atherosclerosis.Recent findingsCD40/CD40L, OX40L/OX40, CD70/CD27 and CD137/CD137L are present in human atherosclerotic plaques and have shown strong immune modulatory functions in atherosclerosis, resulting in either atherogenic or atheroprotective effects in mouse models of atherosclerosis.SummaryInsight into the immune modulatory mechanisms of co-stimulatory interactions in atherosclerosis can contribute to clinical exploitation of these interactions in the treatment of cardiovascular disease.
引用
收藏
页码:518 / 524
页数:7
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