Serum complement components in Henoch-Schönlein purpura

Arch Dis Child. 1978 May;53(5):417-9. doi: 10.1136/adc.53.5.417.

Abstract

Serum levels of C1q, C4, C3, C5, factor B, and properdin were measured in patients with Henoch-Schönlein purpura (HSP). In the cases of acute HSP, 9 of 23 (39%) had a low CH50, and 5 of 17 (30%) a low properdin; C1q, C4, and C3 levels were not depressed. In 10 cases with chronic nephritis following HSP, complement components were normal except for 2 with reduced C4 and one with low properdin. These findings confirm that complement activation occurs in HSP; the low serum levels of properdin in the acute group indicate that there is activation of the alternative pathway in these patients.

MeSH terms

  • Acute Disease
  • Adolescent
  • Child
  • Child, Preschool
  • Chronic Disease
  • Complement C1 / analysis
  • Complement C3 / analysis
  • Complement C4 / analysis
  • Complement C5 / analysis
  • Complement Factor B / analysis
  • Complement System Proteins / analysis*
  • Humans
  • IgA Vasculitis / immunology*
  • Nephritis / immunology
  • Properdin / analysis

Substances

  • Complement C1
  • Complement C3
  • Complement C4
  • Complement C5
  • Properdin
  • Complement System Proteins
  • Complement Factor B