Abstract

BackgroundInfiltration of immune cells into the kidney is one of the key features of lupus nephritis (LN). The presence of immune cells in the urine may be used as a non-invasive biomarker of LN. Here, we aimed to analyze the clinicopathologic significance of urinary CD11c+ macrophages in patients with LN.MethodsThe numbers and proportions of CD11c+ macrophages in the urine samples of patients with LN at the time of kidney biopsy were examined using flow cytometry. We also examined the association between the levels of urinary CD11c+ macrophages and the clinical and pathologic features of patients with LN.ResultsCompared with patients without LN or those with non-proliferative LN, patients with proliferative LN had significantly higher numbers and proportions of urinary CD11c+ macrophages, which were strongly correlated with the serum anti-dsDNA antibody titer. The numbers and proportions of urinary CD11c+ macrophages were significantly associated with the values of chronicity indices such as tubular atrophy and interstitial fibrosis. No significant relationships were found between the levels of urinary CD11c+ macrophages and the activity scores, degree of proteinuria, or lupus disease activity. Urinary CD11c+ macrophages were more abundant in patients who did not achieve renal response to induction treatment with immunosuppressants than in those who achieved complete or partial response. The receiver operating characteristic (ROC) curve analysis showed that the number of urinary CD11c+ macrophages was the most powerful predictor of renal response at 6 months (ROC-AUC = 1.00, p = 0.0004).ConclusionThe urinary levels of CD11c+ macrophages were closely associated with the chronic pathologic changes of LN and renal response and may thus be used as a novel biomarker in LN.

Highlights

  • Infiltration of immune cells into the kidney is one of the key features of lupus nephritis (LN)

  • We found that the numbers and proportions of CD11c+ macrophages among CD45+ cells in the urine significantly correlated with the serum titers of the antidsDNA antibody, which is highly specific to LN (Fig. 1c)

  • We found that the numbers and proportions of CD11c+ macrophages among CD45+ cells in the urine samples, which were collected at the time of kidney biopsy, were significantly associated with the presence of tubular atrophy and interstitial fibrosis (Figs. 2a and 3a)

Read more

Summary

Introduction

Infiltration of immune cells into the kidney is one of the key features of lupus nephritis (LN). The presence of immune cells in the urine may be used as a non-invasive biomarker of LN. LN is initiated after deposition of the immune complex in the glomeruli; tubulointerstitial inflammation is commonly observed in LN. Kidney biopsy is essential for obtaining accurate diagnosis and classification of patients with LN. Several recent studies have detected urinary cells in patients with LN and showed that the kidney-originated cells in the urine of patients with LN had strong correlations with disease activity and may be used as new biomarkers [8,9,10,11]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call