Interferon therapy for Behçet's disease

J Am Acad Dermatol. 1994 Oct;31(4):617-9. doi: 10.1016/s0190-9622(94)70226-8.

Abstract

Background: Behçet's disease was first described in 1937 as a trisymptom complex. No standard therapy has been established. Its cause is presumed to be viral or immunologic.

Objective: We sought to determine whether patients with Behçet's disease benefit from interferon, which has antiviral, immunomodulatory, antiproliferative, and antitumoral properties.

Methods: Fourteen patients were initially given 3 MU interferon alfa-2a subcutaneously three times per week. The doses were gradually increased to 12 MU. Each patient received a total dose of 216 MU during the 2-month study. Therapy with 9 MU interferon alfa-2a once a month was continued in half the patients. All patients were observed before and after treatment for 6-month periods, and all symptoms were recorded.

Results: All patients were symptom free by the end of the 2-month treatment period. The frequencies of oral and genital ulcers as well as pustular vasculitis decreased significantly in the posttreatment period as compared with the pretreatment period.

Conclusion: The data suggest that interferon treatment appears to be effective for patients with Behçet's disease.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Adolescent
  • Adult
  • Behcet Syndrome / pathology
  • Behcet Syndrome / therapy*
  • Female
  • Follow-Up Studies
  • Humans
  • Injections, Subcutaneous
  • Interferon alpha-2
  • Interferon-alpha / administration & dosage
  • Interferon-alpha / adverse effects
  • Interferon-alpha / therapeutic use*
  • Male
  • Middle Aged
  • Recombinant Proteins
  • Remission Induction

Substances

  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins