Long term treatment of rheumatoid arthritis with high doses of intravenous immunoglobulins: effects on disease activity and serum cytokines

Ann Rheum Dis. 1995 May;54(5):382-5. doi: 10.1136/ard.54.5.382.

Abstract

Objective: To evaluate the effects of long term treatment of rheumatoid arthritis (RA) with high doses of intravenous immunoglobulins (IVIg).

Methods: Ten patients with active RA and prior unsuccessful treatment with at least one slow acting antirheumatic drug were treated with 400 mg/kg of IVIg for the first three days and then once a month for 12 months. Clinical evaluation and laboratory analysis were performed every month. Serum levels of tumour necrosis factor alpha (TNF alpha), soluble interleukin-2 receptor (sIL-2R), IL-1 alpha, IL-1 beta, IL-6 and interferon gamma (IFN gamma) were measured at baseline and at three monthly intervals for 15 months.

Results: Although laboratory parameters were not influenced by the treatment, a late but significant clinical improvement was observed after six months. Serial measurement of cytokines revealed a rapid and persistent decrease in serum TNF alpha and a late and significant reduction in sIL-2R concentrations.

Conclusion: This study suggests that IVIg can ameliorate the symptoms and improve the functional capability of RA patients. This effect is associated with a partial modulation of serum concentrations of inflammatory cytokines and, more interestingly, with a late decrease in sIL-2R which correlated with the late reduction in disease activity.

MeSH terms

  • Adult
  • Aged
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / therapy*
  • Cytokines / blood*
  • Drug Administration Schedule
  • Evaluation Studies as Topic
  • Female
  • Humans
  • Immunoglobulins / administration & dosage*
  • Injections, Intravenous
  • Interferon-gamma / analysis
  • Interleukin-1 / analysis
  • Interleukin-6 / analysis
  • Male
  • Middle Aged
  • Receptors, Interleukin-2 / analysis
  • Time Factors
  • Tumor Necrosis Factor-alpha / analysis

Substances

  • Cytokines
  • Immunoglobulins
  • Interleukin-1
  • Interleukin-6
  • Receptors, Interleukin-2
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma