Defective reticuloendothelial system Fc-receptor function in systemic lupus erythematosus

N Engl J Med. 1979 Mar 8;300(10):518-23. doi: 10.1056/NEJM197903083001002.

Abstract

To determine whether reticuloendothelial-system immunospecific Fc-receptor function is abnormal in patients with systemic lupus erythematosus, we studied the clearance of IgG-sensitized 51Cr-labeled erythrocytes by these splenic macrophage membrane receptors in 15 untreated patients. Fc-specific clearance rates were strikingly abnormal in 13 of 15 patients (half-times ranging from 80 to 2256 minutes, P less than 0.001 as compared to controls). Abnormal clearances correlated with immune-complex levels (as measured by the C1q-binding assay) and with disease activity. C1q-binding activity and anti-DNA titers also correlated with disease activity. The correlations of C3, C4, CH50 and factor B with abnormal clearance and disease activity were weaker or nonexistent. The significant correlations among clearance, disease activity and C1q-binding activity suggest that the defect in Fc-receptor function may lead to the prolonged circulation of immune complexes, thereby contributing to tissue deposition and damage.

MeSH terms

  • Adult
  • Antigen-Antibody Complex / analysis
  • Autoantibodies / analysis
  • Binding Sites, Antibody
  • Complement C1 / analysis
  • Complement System Proteins / analysis
  • DNA / immunology
  • Erythrocytes / immunology
  • Female
  • Humans
  • Immunoglobulin Fc Fragments / immunology*
  • Immunoglobulin G / immunology
  • Lupus Erythematosus, Systemic / immunology*
  • Lupus Erythematosus, Systemic / physiopathology
  • Macrophages / immunology
  • Male
  • Middle Aged
  • Mononuclear Phagocyte System / immunology*
  • Mononuclear Phagocyte System / physiopathology
  • Receptors, Antigen, B-Cell / analysis

Substances

  • Antigen-Antibody Complex
  • Autoantibodies
  • Complement C1
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Receptors, Antigen, B-Cell
  • Complement System Proteins
  • DNA