Messenger RNA expression of RANTES in the urinary sediment of patients with lupus nephritis

被引:26
作者
Chan, Rebecca Wing-Yan
Lai, Fernand Mac-Moune
Li, Edmund Kwok-Ming
Tam, Lai-Shan
Chow, Kai-Ming
Li, Philip Kam-Tao
Szeto, Cheuk-Chun [1 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anat & Cellular Pathol, Shatin, Hong Kong, Peoples R China
关键词
chemokine; systematic lupus erythematosus; urinary sediment;
D O I
10.1111/j.1440-1797.2006.00565.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Lupus nephritis is characterized by intra-renal inflammation. Patients with systemic lupus erythematosus (SLE) showed abnormal T-cell expression of RANTES (regulated upon activation, normal T cell expressed) and its level in their serum. The authors studied the mRNA expression of RANTES in the urinary sediment of lupus patients. Methods: The authors studied 88 lupus patients, who were classified into active, remission and non-renal SLE groups according to the disease activity, 29 non-SLE and 10 healthy controls. Lupus activity was assessed by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI). Urinary mRNA expression of RANTES was studied by real-time quantitative polymerase chain reaction. Results: The expression of RANTES in urinary sediment was significantly elevated in active group (P < 0.001). Expression level of RANTES correlated with the SLEDAI score (r = 0.57; P < 0.001) and renal score in SLEDAI (r = 0.60; P < 0.001). In addition, urinary expression of RANTES had significant correlation with degree of proteinuria, serum creatinine, albumin and estimated glomerular filtration rate. Conclusion: The authors conclude that the mRNA expression of RANTES was elevated in the urinary sediment of patients with active lupus nephritis. Measurement of urinary mRNA expression may be a novel non-invasive method for the assessment of lupus disease activity and the severity of renal involvement.
引用
收藏
页码:219 / 225
页数:7
相关论文
共 33 条
[1]  
*ABL PRISM, 1997, US B ABL PRISM, V2
[2]  
Anders HJ, 2001, J AM SOC NEPHROL, V12, P919, DOI 10.1681/ASN.V125919
[3]   Chemokines and leukocyte traffic [J].
Baggiolini, M .
NATURE, 1998, 392 (6676) :565-568
[4]   DERIVATION OF THE SLEDAI - A DISEASE-ACTIVITY INDEX FOR LUPUS PATIENTS [J].
BOMBARDIER, C ;
GLADMAN, DD ;
UROWITZ, MB ;
CARON, D ;
CHANG, CH .
ARTHRITIS AND RHEUMATISM, 1992, 35 (06) :630-640
[5]   Mesangial expansion associated with glomerular endothelial cell activation and macrophage recruitment is developing in hyperlipidaemic apoE null mice [J].
Bruneval, P ;
Bariéty, J ;
Lair, MF ;
Mandet, C ;
Heudes, D ;
Nicoletti, A .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2002, 17 (12) :2099-2107
[6]  
CHAN RW, 2004, J AM SOC NEPHROL, V15, pA500
[7]   Expression of chemokine and fibrosing factor messenger RNA in the urinary sediment of patients with lupus nephritis [J].
Chan, RWY ;
Lai, FMM ;
Li, EKM ;
Tam, LS ;
Wong, TYH ;
Szeto, CYK ;
Li, PKT ;
Szeto, CC .
ARTHRITIS AND RHEUMATISM, 2004, 50 (09) :2882-2890
[8]   Inflammatory cytokine gene expression in the urinary sediment of patients with lupus nephritis [J].
Chan, RWY ;
Tam, LS ;
Li, EKM ;
Lai, FMM ;
Chow, KM ;
Lai, KB ;
Li, PKT ;
Szeto, CC .
ARTHRITIS AND RHEUMATISM, 2003, 48 (05) :1326-1331
[9]   Laser microdissection and gene expression analysis on formaldehyde-fixed archival tissue [J].
Cohen, CD ;
Gröne, HJ ;
Gröne, EF ;
Nelson, PJ ;
Schlöndorff, D ;
Kretzler, M .
KIDNEY INTERNATIONAL, 2002, 61 (01) :125-132
[10]  
De Lema GP, 2001, J AM SOC NEPHROL, V12, P1369, DOI 10.1681/ASN.V1271369