Prevalence of circulating immune complexes in patients with cystic fibrosis and arthritis

N M Wulffraat, E R de Graeff-Meeder, G T Rijkers, H van der Laag, W Kuis

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We report the clinical and laboratory characteristics of eight patients with cystic fibrosis (CF) and arthropathy. Five patients had frequently relapsing, episodic arthritis; one had chronic arthritis with high titers of rheumatoid factors that could not be distinguished from juvenile chronic arthritis. In two patients the arthropathy did not relapse. Forty-six patients with CF but without arthropathy, seen during the same 1-year period, served as control subjects. Results of lung function tests and sputum cultures were similar in both groups. The sera of six of the eight patients with CF-arthropathy had high levels of circulating immune complexes, measured both by C1q-binding and the indirect granulocyte phagocytosis test, whereas only 1 of 12 control patients tested had positive C1q binding (p < 0.023). Serum complement levels were normal in both groups. Synovial biopsies, performed in three patients, showed only scanty lymphocytic infiltrates; immunofluorescent staining showed deposits of IgM, IgG, and components of complement C1q, C3, and C4. These findings suggest that the arthropathy found in CF is an immune-mediated phenomenon.

Original languageEnglish
Pages (from-to)374-8
Number of pages5
JournalJournal of Pediatrics
Volume125
Issue number3
Publication statusPublished - Sept 1994

Keywords

  • Adolescent
  • Adult
  • Antigen-Antibody Complex
  • Arthritis
  • Child
  • Child, Preschool
  • Complement C1q
  • Cystic Fibrosis
  • Female
  • Fluorescent Antibody Technique
  • Follow-Up Studies
  • Humans
  • Immunoglobulin A
  • Immunoglobulin G
  • Immunoglobulin M
  • Infant
  • Lung
  • Male
  • Prevalence
  • Recurrence
  • Retrospective Studies
  • Rheumatoid Factor
  • Synovial Membrane
  • Journal Article

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