Endothelial cell dysfunction in systemic vasculitis: new developments and therapeutic prospects

被引:62
作者
Bacon, PA [1 ]
机构
[1] Univ Birmingham, Sch Med, Div Immun & Infect, Dept Rheumatol, Birmingham G15 2TT, W Midlands, England
关键词
systemic vasculitis; endothelial cell dysfunction;
D O I
10.1097/01.bor.0000149084.16639.b0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review The role of the endothelium as an active player rather than a passive victim of inflammation has received considerable interest in atherosclerosis, but less so in systemic vasculitis (SV).'However, the accumulating multi-organ damage seen in SV probably includes the endothelium Assessment of endothelial function is now a stardard clinical research tool in cardtosvascular.depart m nts`Me, exciting insights provided by their application to SV both primary disease and connective tissue diseases (CTD), is reviewed here. Recent findings Diffuse endothelial cell dysfunction (ECD) documented by several techniques occurs commonly in adult and childhood SV. Similar ECD is also seen in CTD. The mechanisms probably relate to inflammatory inflammatory cytokines such as TNF. The particular role of vasculitic, as opposed to synovial or internal organ inflammation, may be release of secondary mediators directly into the blood stream-whence they can reach distant endothelial beds to induce this diffuse ECD. Summary Endothelial injury is the first step in atherosclerosis,where peripheral abnormalities correlate with coronary artery responses. The diffuse ECD in CTD suggests that vascular inflammation ay initiate the: accelerated CVS disease there. The new findings of similar ECD in primary SV predicts enhanced atherosclerosis here too. In Kawasaki syndrome, persistent late ECD correlates with abnormal coronary responses. In adult SV, initial data also suggests increased subclinical atherosclerosis. The role of endothelial function in the clinical outcome of SV deserves more attention. Research-to. pinpoint the mechanisms of ECD should lead to more specific therapies that may ameliorate the continuing late morbidity and mortality of SV.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 61 条
[31]  
Lamprecht P, 2004, HERZ, V29, P47, DOI 10.1007/s00059-004-2525-0
[32]   Differences in CCR5 expression on peripheral blood CD4+CD28- T-cells and in granulomatous lesions between localized and generalized Wegener's granulomatosis [J].
Lamprecht, P ;
Bruhl, H ;
Erdmann, A ;
Holl-Ulrich, K ;
Csernok, E ;
Seitzer, U ;
Mack, M ;
Feller, AC ;
Reinhold-Keller, E ;
Gross, WL ;
Muller, A .
CLINICAL IMMUNOLOGY, 2003, 108 (01) :1-7
[33]  
Lima DSN, 2002, J RHEUMATOL, V29, P292
[34]   Perturbation of the T-cell repertoire in patients with unstable angina [J].
Liuzzo, G ;
Kopecky, SL ;
Frye, RL ;
O'Fallon, WM ;
Maseri, A ;
Goronzy, JJ ;
Weyand, CM .
CIRCULATION, 1999, 100 (21) :2135-2139
[35]   Shed membrane microparticles with procoagulant potential in human atherosclerotic plaques -: A role for apoptosis in plaque thrombogenicity [J].
Mallat, Z ;
Hugel, B ;
Ohan, J ;
Lesèche, G ;
Freyssinet, JM ;
Tedgui, A .
CIRCULATION, 1999, 99 (03) :348-353
[36]   Elevated levels of shed membrane microparticles with procoagulant potential in the peripheral circulating blood of patients with acute coronary syndromes [J].
Mallat, Z ;
Benamer, H ;
Hugel, B ;
Benessiano, J ;
Steg, PG ;
Freyssinet, JM ;
Tedgui, A .
CIRCULATION, 2000, 101 (08) :841-843
[37]  
Mueller A, 2003, CLIN EXP RHEUMATOL, V21, pS49
[38]  
Murakami H, 2003, CIRC J, V67, P273
[39]   Circulating endothelial cells in Kawasaki disease [J].
Nakatani, K ;
Takeshita, S ;
Tsujimoto, H ;
Kawamura, Y ;
Tokutomi, T ;
Sekine, I .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 131 (03) :536-540
[40]   Effect of plasma from patients with Behcet's disease on the production of nitric oxide in cultured human umbilical vein endothelial cells [J].
Örem, A ;
Ertürk, M ;
Çimsit, G ;
Kural, BV .
MEDICAL PRINCIPLES AND PRACTICE, 2004, 13 (01) :35-38