C1qRP (CD93) expression on peripheral blood monocytes in patients with systemic lupus erythematosus

Frank Moosig1, Erika Fähndrich, Anja Knorr-Spahr

  • 1Second Medical Department, University Hospital of Schleswig Holstein, Campus Kiel, Chemnitzstr. 33, 24116 Kiel, Germany. F.Moosig@med2.uni-kiel.de

Insights

Systemic lupus erythematosus (SLE) patients show no difference in monocyte C1qRp (CD93) expression compared to healthy controls. Glucocorticoid dosage, not SLE itself, influenced C1qRp levels, while LPS stimulation upregulated expression in all subjects.

Area of Science:

  • Immunology
  • Rheumatology
  • Cell Biology

Background:

  • Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by immune dysregulation.
  • Monocyte C1qRp (CD93) is a cell surface receptor implicated in immune responses.
  • Understanding C1qRp expression in SLE is crucial for elucidating disease mechanisms.

Purpose of the Study:

  • To compare C1qRp (CD93) expression on monocytes in SLE patients versus healthy controls (HC).
  • To investigate the impact of glucocorticoids and lipopolysaccharide (LPS) on C1qRp expression in SLE and HC.
  • To determine if C1qRp expression is altered in SLE patients.

Main Methods:

  • Flow cytometry was used to analyze C1qRp expression on monocytes.
  • Thirty-six SLE patients and 20 HC were recruited.
  • In vitro experiments involved culturing monocytes and stimulating them with dexamethasone, interferon-gamma, and LPS.

Main Results:

  • No significant difference in C1qRp expression was observed between SLE patients and HC.
  • SLE patients on lower-dose or no steroids exhibited higher C1qRp expression than those on higher doses.
  • In vitro dexamethasone did not alter C1qRp expression, whereas LPS significantly upregulated it in both groups.

Conclusions:

  • C1qRp expression and its regulation appear unaltered in SLE patients.
  • Glucocorticoid therapy may influence C1qRp expression levels.
  • Further research is needed to explore the relationship between C1qRp, disease activity, and medication in SLE.

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