Low dose oral interferon alpha 2a in HIV-1 seropositive patients: a double-blind, placebo-controlled trial.

S E Wright, D P Hutcheson, J M Cummins
Author Information
  1. S E Wright: Veterans Affairs Medical Center and Department of Internal Medicine, Texas Tech University Health Sciences Center, Amarillo, USA.

Abstract

Low dose oral interferon alpha has been shown to be of benefit in viral disease in animals. In a double-blind, placebo-controlled trial, 177 patients seropositive for HIV-1 were randomly assigned to receive placebo or recombinant human interferon alpha 2a (rIFN alpha). Endpoints were survival, alteration of disease classification, performance, and changes in CD4+ T cell numbers. There was a trend for improved survival in the group receiving rIFN alpha at the dose of 1.0 IU/lb. The changes in disease classification or in weight were not significantly different. Performance was improved to a greater extent (p=0.1) in the patients who received the two higher rIFN alpha dosages (1.0 IU/lb and 10.0 IU/lb) at 6 months. In addition, the CD4+ T cell count was improved only in the 1.0 IU/lb dose treatment group at 6 months. Treatment with low dose oral interferon at 1.0 IU/lb was associated with improved CD4+ T cell count, performance and a trend toward enhanced survival in HIV seropositive patients. These differences were, however, not statistically significant. A larger study, with better return rate, will be needed to determine whether low dose, oral interferon alpha is actually beneficial for these patients.

MeSH Term

Animals
CD4 Lymphocyte Count
Double-Blind Method
HIV Seropositivity
HIV-1
Humans
Interferon alpha-2
Interferon-alpha
Recombinant Proteins
Survival Rate

Chemicals

Interferon alpha-2
Interferon-alpha
Recombinant Proteins

Word Cloud

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