Involvement of dendritic cells in long-term aortocoronary saphenous vein bypass graft failure

被引:13
作者
Cherian, SM
Bobryshev, YV
Inder, SJ
Lord, RSA
Reddi, KH
Farnsworth, E
Tran, D
Munro, VF
Ashwell, KWS
机构
[1] St Vincents Hosp, Professorial Surg Unit, Darlinghurst, NSW 2010, Australia
[2] Univ New S Wales, Sch Anat, Sydney, NSW 2052, Australia
[3] St Vincents Hosp, Dept Cardiothorac Surg, Darlinghurst, NSW 2010, Australia
[4] St Vincents Hosp, Div Anat Pathol, Darlinghurst, NSW 2010, Australia
来源
CARDIOVASCULAR SURGERY | 1999年 / 7卷 / 05期
关键词
aortocoronary artery saphenous vein bypass graft; atherogenesis; atherosclerosis; calcification; dendritic cells; S-100; protein;
D O I
10.1016/S0967-2109(99)00021-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Antigen-presenting dendritic cells are present in atherosclerotic lesions in human arterial intima, but have not been investigated in atherosclerotic and hyperplastic stenotic lesions that affect vein grafts used as arterial conduits. This study was undertaken to examine whether dendritic cells are present in aortocoronary artery saphenous vein bypass grafts affected by high-grade atheromatous stenosis. Stenotic saphenous vein coronary artery bypass grafts (angiographic luminal stenosis > 75%) were harvested from 10 patients (nine male, one female), aged 42-71 years (mean 56.5) at re-do operation. The mean time interval from bypass surgery to the excision of stenotic grafts was 11.5 years (range 2-21). The specimens were fixed in 10% buffered formalin, embedded in paraffin blocks and the sections stained with antibodies to S-100 (to identify dendritic cells), CD3 (T cells), CD68 (macrophages), von Willebrand factor (endothelial cells) and a-smooth muscle actin (smooth muscle cells) using avidin-biotin complex immunoperoxidase technique. Normal veins were obtained during saphenous vein femoro-popliteal grafting. The stenotic venous grafts showed histological features typical of extensive arterialization, intimal hyperplasia, atherosclerotic plaque-like lesions, calcification and thrombosis. In areas of intimal hyperplasia, S-100-positive cells were distributed irregularly among smooth muscle cells. S-100-positive dendritic cells were seen most frequently within atherosclerotic plaque-like lesions where they co-localized with CD3(+) cells and CD68(+) cells. S-100-positive dendritic cells were also seen accumulating within calcific foci. No S-100-positive cells were found in normal, ungrafted saphenous veins. We conclude that dendritic cells are present in aortocoronary saphenous vein bypass grafts affected by high grade stenosis. Dendritic cells are probably involved in immune mechanisms of atherogenesis through their interactions with T cells and macrophages, The accumulation of dendritic cells within calcific foci suggests their contribution to the calcification of stenotic venous grafts. (C) 1999 The International Society for Cardiovascular Surgery. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:508 / 518
页数:11
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