Urinary Soluble CD163 Levels Predict IgA Nephropathy Remission Status

Front Immunol. 2021 Dec 23:12:769802. doi: 10.3389/fimmu.2021.769802. eCollection 2021.

Abstract

Noninvasive biomarkers of disease activity are needed to predict disease remission status in patients with IgA nephropathy (IgAN). Soluble CD163 (sCD163), shed by monocytes and macrophages, is a potential biomarker in diseases associated with excessive macrophage activation. We investigated the association of urinary sCD163 (u-sCD163) with histopathological activity and clinical manifestations in 349 patients with biopsy-diagnosed IgAN. U-sCD163 was measured via enzyme-linked immunosorbent assay. In patients with IgAN, higher u-sCD163 levels were associated with histological lesions of greater severity, as well as more proteinuria and poorer renal function. Additionally, u-sCD163 was correlated with infiltration of tubulointerstitial CD163+ macrophages. High u-sCD163 levels (>3.57 ng/mg Cr) were associated with a 2.66-fold greater risk for IgAN remission failure in adjusted analyses. Adding u-sCD163 levels to the model containing clinical data at biopsy and MEST-C score significantly improved the risk prediction of IgAN remission status (AUC 0.788). Together, our results suggest that u-sCD163 may be a useful noninvasive biomarker to evaluate disease severity and remission status of IgAN.

Keywords: IgA nephropathy; biomarker; macrophages; remission status; urinary soluble CD163.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD / urine*
  • Antigens, Differentiation, Myelomonocytic / urine*
  • Biomarkers / urine*
  • CD163 Antigen
  • Female
  • Glomerulonephritis, IGA / diagnosis
  • Glomerulonephritis, IGA / urine*
  • Humans
  • Kidney / pathology
  • Macrophages / metabolism
  • Macrophages / pathology
  • Male
  • Middle Aged
  • Predictive Value of Tests
  • Prognosis
  • Receptors, Cell Surface
  • Remission, Spontaneous
  • Retrospective Studies
  • Severity of Illness Index*
  • Solubility

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers
  • CD163 Antigen
  • Receptors, Cell Surface