Treatment of human immunodeficiency virus infection with hydroxyurea: virologic and clinical evaluation

J Infect Dis. 1996 Jul;174(1):204-9. doi: 10.1093/infdis/174.1.204.

Abstract

To assess the efficacy of the therapeutic use of inhibitors of ribonucleotide reductase for the treatment of human immunodeficiency virus (HIV) type 1 infection, 7 consecutive patients were enrolled in a clinical trial involving monotherapy with hydroxyurea for 8-19 weeks. During therapy, patients were evaluated for clinical status and immunologic, hematologic, and quantitative virologic parameters, including determinations of viremia and the number of provirus-containing cells by competitive polymerase chain reaction. In all patients, these parameters were not modified during the course of therapy. The number of CD4 cells remained generally unchanged or showed a tendency to further decline. No sign of improvement in HIV disease was detected in any patient. These observations indicate that monotherapy with hydroxyurea does not provide therapeutic benefit to HIV-1-infected patients.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / drug therapy*
  • Acquired Immunodeficiency Syndrome / immunology
  • Adult
  • Aged
  • Antiviral Agents / therapeutic use*
  • DNA, Viral / blood
  • Enzyme Inhibitors / therapeutic use*
  • Female
  • HIV Core Protein p24 / blood
  • HIV-1 / genetics
  • Humans
  • Hydroxyurea / therapeutic use*
  • Leukocyte Count
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • RNA, Viral / blood
  • Time Factors
  • Treatment Outcome

Substances

  • Antiviral Agents
  • DNA, Viral
  • Enzyme Inhibitors
  • HIV Core Protein p24
  • RNA, Viral
  • Hydroxyurea