NDT Advance Access published online on January 31, 2006
Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfk102
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1 Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong, China
* To whom correspondence should be addressed. Background. Previous studies have shown that messenger RNA (mRNA) expression of target genes is increased in the urinary sediment of patients with active lupus. We study the effect of immunosuppressive therapy on the urinary gene expression profile in patients with active lupus nephritis. Method. We recruited nine patients with active systemic lupus erythematosus (SLE) and renal disease, and required corticosteroid, with or without cytotoxic treatment. They were followed for 6 months, urine samples were collected at 0, 4, 12 and 24 weeks and gene expression profile was determined by polymerase chain reactions. The pattern of gene expression was compared to clinical parameters of therapeutic response. Results. Amongst the target genes studied, there was a progressive decline in the urinary expression of T-bet, interleukin (IL)-10, transforming growth factor-beta (TGF- Conclusions. The mRNA expression of T-bet, IL-10, TGF-
Received September 6, 2005
Accepted January 5, 2006
Original Article
The Effect of immunosuppressive therapy on the messenger RNA expression of target genes in the urinary sediment of patients with active lupus nephritis
Rebecca Wing-Yan Chan 1,
Fernand Mac-Moune Lai 2,
Edmund Kwok-Ming Li 1,
Lai-Shan Tam 1,
Kai-Ming Chow 1,
Philip Kam-Tao Li 1,
and
Cheuk-Chun Szeto 1 *
2 Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong, China
Cheuk-Chun Szeto, E-mail: ccszeto{at}cuhk.edu.hk
Abstract 
), monocyte chemoattractant protein-1 (MCP-1), and interferon-gamma (IFN-
) after immunosuppressive treatment, although the change of IFN- was not statistically significant. The time course of their urinary expression was parallel to the systemic activity as reflected by the systemic lupus erythematosus disease activity index (SLEDAI). Throughout the study period, the SLEDAI score correlated significantly with the expressions of IFN- (r = 0.43, P = 0.009), T-bet (r = 0.40, P = 0.016), TGF- (r = 0.51, P = 0.002) and MCP-1 (r = 0.38, P = 0.022). The anti-double strand(anti-ds)DNA antibody titer correlated significantly with the expressions of IFN- (r = 0.45, P = 0.009), T-bet (r = 0.37, P = 0.034), IL-10 (r = 0.59, P<0.001), TGF- (r = 0.44, P = 0.010) and MCP-1 (r = 0.49, P = 0.004). On the other hand, the expression level of IL-2, IL-4, IL-12, IL-18 and GATA-3 remained static throughout the study period., MCP-1, and probably IFN- in the urinary sediment of patients with active lupus nephritis improves with successful immunosuppressive therapy, and the change in gene expression profile is in phase with the clinical disease activity. Measurement of urinary mRNA expression of target genes may be a potential non-invasive tool for the monitoring of lupus disease activity.
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