Circulating soluble adhesion molecules in ANCA-associated vasculitis

被引:38
作者
Ara, J
Mirapeix, E
Arrizabalaga, P
Rodriguez, R
Ascaso, C
Abellana, R
Font, J
Darnell, A
机构
[1] Univ Barcelona, Inst Invest Biomed August Pi & Sunyer, Hosp Clin, Serv Nephrol, E-08036 Barcelona, Spain
[2] Univ Barcelona, Inst Invest Biomed August Pi & Sunyer, Hosp Clin, Biostat & Epidemiol Unit, E-08036 Barcelona, Spain
[3] Univ Barcelona, Inst Invest Biomed August Pi & Sunyer, Hosp Clin, Autoimmune Dis Unit, E-08036 Barcelona, Spain
关键词
ANCA-associated vasculitis; disease activity; microscopic polyangiitis; soluble adhesion molecules; Wegener's; granulomatosis;
D O I
10.1093/ndt/16.2.276
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. To evaluate whether changes in concentrations of soluble (s) E-selectin, sP-selectin, sL-selectin, intercellular adhesion molecule I (sICAM-1), and vascular cell adhesion molecule 1 (sVCAM-1) reflect disease activity in patients with ANCA-associated vasculitis and whether serum levels of these adhesion molecules are related to the degree of renal failure in patients with chronic renal failure (CRF). Subjects and methods. A sandwich ELISA was used to measure these soluble adhesion molecules in (ii) sera from 20 patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (10 patients with Wegener's granulomatosis (WG) and 10 patients with microscopic polyangiitis (MPA)), obtained at the time of diagnosis and during the remission period; (ii) sera from 40 patients with CRF not undergoing haemodialysis. Results. At the time of diagnosis, serum levels of sE-selectin, sICAM-1 and sVCAM-1 (88 +/- 42 ng/ml, 437 +/- 184 ng/ml, 1720 +/- 1174 ng/ml respectively) were significantly higher in patients with ANCA-associated vasculitis than in healthy controls (P < 0.0001, P = 0.002 and P = 0.001 respectively). Serum sP-selectin values did not differ from those obtained in normal donors. In contrast, sl-selectin levels (940 <plus/minus> 349 ng;ml) were significantly lower in patients than those recorded in healthy controls (P < 0.0001). A significant decrease in concentrations of sE-selectin, sP-selectin, sICAM-1, and sVCAM-1 was observed between active and remission phases (P < 0.0001, P = 0.002, P=0.001 and P = 0.001 respectively). No significant differences were observed in sL-selectin levels between active and remission phases. sl-selectin concentrations (802 +/- 306 ng/ml) during the remission phase remained lower than those observed in healthy controls (P < 0.0001). No correlation was observed between serum creatinine and sE-selectin, sP-selectin, sICAM-1 and sVCAM-1 in patients of the CRF group. A slight negative correlation was established between creatinine and sl-selectin concentration. Conclusions. Increased serum levels of sE-selectin, sICAM-1, and sVCAM-1 and decreased levels of sl-selectin in active ANCA-associated vasculitis, and the normalization of sE-selectin, sICAM-1, and sVCAM-1 during the remission phase suggest that the concentration of soluble levels of these adhesion molecules reflects disease activity. The decrease in sP-selectin levels between active and inactive phases also suggest that this receptor may reflect clinical activity. The lack of correlation between serum levels of sE-selectin, sP-selectin. sICAM-1, and sVCAM-1 and the degree of renal failure in patients with CRF Suggests that the mechanism of clearance of these molecules is not renal.
引用
收藏
页码:276 / 285
页数:10
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