The Role of Immunomodulation in Vein Graft Remodeling and Failure

被引:15
作者
Baganha, Fabiana [1 ,2 ,3 ]
de Jong, Alwin [1 ,2 ]
Jukema, J. Wouter [4 ]
Quax, Paul H. A. [1 ,2 ]
de Vries, Margreet R. [1 ,2 ]
机构
[1] Leiden Univ, Med Ctr, Dept Vasc Surg, POB 9600, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Einthoven Lab Expt Vasc Med, POB 9600, NL-2300 RC Leiden, Netherlands
[3] Univ Aberdeen, Aberdeen Cardiovasc & Diabet Ctr, Inst Med Sci, Aberdeen, Scotland
[4] Leiden Univ, Med Ctr, Dept Cardiol, Leiden, Netherlands
关键词
Cardiovascular diseases; Bypass graft; Vein graft failure; Innate and adaptive immunity; Vascular remodeling; CABG; MONOCYTE CHEMOATTRACTANT PROTEIN-1; EARLY GROWTH RESPONSE-1; COMPLEMENT FACTOR C5A; SMOOTH-MUSCLE-CELLS; SAPHENOUS-VEIN; NEOINTIMAL HYPERPLASIA; BYPASS GRAFTS; INTIMAL HYPERPLASIA; GENE-THERAPY; AORTOCORONARY BYPASS;
D O I
10.1007/s12265-020-10001-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obstructive arterial disease is a major cause of morbidity and mortality in the developed world. Venous bypass graft surgery is one of the most frequently used revascularization strategies despite its considerable short and long time failure rate. Due to vessel wall remodeling, inflammation, intimal hyperplasia, and accelerated atherosclerosis, vein grafts may (ultimately) fail to revascularize tissues downstream to occlusive atherosclerotic lesions. In the past decades, little has changed in the prevention of vein graft failure (VGF) although new insights in the role of innate and adaptive immunity in VGF have emerged. In this review, we discuss the pathophysiological mechanisms underlying the development of VGF, emphasizing the role of immune response and associated factors related to VG remodeling and failure. Moreover, we discuss potential therapeutic options that can improve patency based on data from both preclinical studies and the latest clinical trials. This review contributes to the insights in the role of immunomodulation in vein graft failure in humans. We describe the effects of immune cells and related factors in early (thrombosis), intermediate (inward remodeling and intimal hyperplasia), and late (intimal hyperplasia and accelerated atherosclerosis) failure based on both preclinical (mouse) models and clinical data.
引用
收藏
页码:100 / 109
页数:10
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