HIV-1 recombinant gp160 vaccine given in accelerated dose schedules. NIAID AIDS Vaccine Clinical Trials Network

Clin Exp Immunol. 1994 Nov;98(2):178-84. doi: 10.1111/j.1365-2249.1994.tb06122.x.

Abstract

The purpose of this randomized, double-blind study was to test the safety and immunogenicity of an HIV-1LAI recombinant gp160 (rgp160) vaccine in healthy, uninfected volunteers using accelerated dosing schedules. Thirty volunteers were randomly assigned to receive 50-micrograms doses of rgp160 in one of two immunization schedules. Group 1 received rgp160 at times 0, 1, 2 and 5 months; and group 2 received rgp160 at times 0, 1, 2, 3 and 4 months. The vaccine was safe and stimulated high levels of HIV-1 envelope-specific binding antibody and T cell memory. There was a trend (P < 0.10) suggesting neutralizing antibodies were better induced by the regimen incorporating a rest period before the final immunization in group 1 volunteers. Both accelerated immunization schedules induced immune responses at levels similar to or better than those achieved by four rgp160 vaccine injections given over 12-18 months in other studies.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • AIDS Vaccines / administration & dosage*
  • AIDS Vaccines / immunology
  • Adult
  • Amino Acid Sequence
  • Analysis of Variance
  • Double-Blind Method
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Gene Products, env / immunology
  • HIV Envelope Protein gp160
  • Humans
  • Immunization Schedule
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Protein Precursors / immunology
  • Vaccines, Synthetic / administration & dosage*
  • Vaccines, Synthetic / immunology

Substances

  • AIDS Vaccines
  • Gene Products, env
  • HIV Envelope Protein gp160
  • Protein Precursors
  • Vaccines, Synthetic