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Systemic interferon-alpha in the treatment of HTLV-I-associated myelopathy.

Abstract
Treatment with interferon-alpha (IFN-alpha) was undertaken in 16 patients with human T-lymphotropic virus type I-associated myelopathy (HAM). All patients had progressive spastic paraparesis before treatment. Twelve patients were enrolled in an open therapeutic trial with a dose of 3.0 x 10(6) IU/day of IFN-alpha and 4 in a randomized, double-blind, multidose (3.0 x 10(6), 1.0 x 10(6) or 0.3 x 10(6) IU/day) trial. IFN-alpha was injected intramuscularly for 28 days. Eight of 12 patients enrolled in an open trial and 2 patients receiving a dose of 3.0 x 10(6) IU/day of IFN-alpha in a randomized trial showed clinical improvements during and after the treatment. The results showed that, although not for all patients, systemic IFN-alpha with a dose of 3.0 x 10(6) IU/day is effective in the treatment of HAM.
AuthorsY Kuroda, K Kurohara, F Fujiyama, H Takashima, C Endo, M Matsui, R Neshige, R Kakigi
JournalActa neurologica Scandinavica (Acta Neurol Scand) Vol. 86 Issue 1 Pg. 82-6 (Jul 1992) ISSN: 0001-6314 [Print] Denmark
PMID1519481 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • HTLV-I Antibodies
  • Interferon-alpha
Topics
  • Adult
  • Aged
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Female
  • HTLV-I Antibodies (analysis)
  • Humans
  • Injections, Intramuscular
  • Interferon-alpha (administration & dosage)
  • Male
  • Middle Aged
  • Neurologic Examination (drug effects)
  • Paraparesis, Tropical Spastic (immunology, therapy)

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