Abstract

IntroductionLupus nephritis (LN) is a severe and frequent manifestation of systemic lupus erythematosus (SLE). Early detection of initial renal manifestations and relapses during follow-up is pivotal to prevent loss of renal function. Apart from renal biopsies, current urinary and serological diagnostic tests fail to accurately demonstrate the presence of active LN. Previously, we demonstrated that effector memory T-cells (CD45RO+CCR7-;TEM) migrate into the urine during active LN. The objective of this study was to assess the diagnostic value of urinary T-cells in comparison with traditional markers of active LN.MethodsT-cells in the urine during active LN and remission were investigated. Twenty-two, in most cases biopsy-proven, active LN patients and 24 SLE patients without active LN were enrolled and serial measurements were performed in 16 patients.ResultsAnalysis of the urinary sediment in active renal disease showed an increased number of CD8+ T-cells and absence of these cells during remission. Enumerating T-cell counts in LN patients with a history of renal involvement was a superior marker of active LN in comparison to traditional markers, such as proteinuria and s-creatinine.ConclusionsIn conclusion, urinary T-cells, in particular CD8+ T cells, are a promising marker to assess renal activity in LN patients, in particular in those with prior renal involvement.

Highlights

  • Lupus nephritis (LN) is a severe and frequent manifestation of systemic lupus erythematosus (SLE)

  • One active LN patient presented without urinary T-cells, which means a sensitivity of 95%

  • The median count of urinary CD4+ T-cells was significantly increased in active LN patients in comparison to inactive LN patients (128 (0 to 1,250 cells/ml) vs. 5 (0 to 136 cells/ml), respectively (P

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Summary

Introduction

Lupus nephritis (LN) is a severe and frequent manifestation of systemic lupus erythematosus (SLE). Apart from renal biopsies, current urinary and serological diagnostic tests fail to accurately demonstrate the presence of active LN. We demonstrated that effector memory T-cells (CD45RO+CCR7-;TEM) migrate into the urine during active LN. The objective of this study was to assess the diagnostic value of urinary T-cells in comparison with traditional markers of active LN. Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by manifestations in multiple organs. Inflammation of the kidneys, in particular, is associated with an unfavorable prognosis [1,2]. The precise pathogenesis of lupus nephritis (LN) has not been fully elucidated, kidney infiltrating T-cells seem to contribute to the inflammatory pathology of LN [3]

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