Tipranavir inhibits broadly protease inhibitor-resistant HIV-1 clinical samples

AIDS. 2000 Sep 8;14(13):1943-8. doi: 10.1097/00002030-200009080-00009.

Abstract

Objective: Although the use of HIV-1 protease inhibitors (PI) has substantially benefited HIV-1-infected individuals, new PI are urgently needed, as broad PI resistance and therapy failure is common.

Methods: The antiviral activity of tipranavir (TPV), a non-peptidic PI, was assessed in in vitro culture for 134 clinical isolates with a wide range of resistance to currently available peptidomimetic PI. The susceptibility of all 134 variants was then re-tested with the four PI simultaneously with TPV, using the Antivirogram assay.

Results: Of 105 viruses with more than tenfold resistance to three or four PI and an average of 6.1 PI mutations per sample, 95 (90%) were susceptible to TPV; eight (8%) had four- to tenfold resistance to TPV and only two (2%) had more than tenfold resistance.

Conclusions: The substantial lack of PI cross-resistance to TPV shown by highly PI-resistant clinical isolates makes TPV an attractive new-generation HIV inhibitor.

MeSH terms

  • Drug Resistance, Microbial
  • Genotype
  • HIV Infections / virology
  • HIV Protease / genetics
  • HIV Protease Inhibitors / pharmacology*
  • HIV-1 / drug effects*
  • HIV-1 / enzymology
  • HIV-1 / genetics
  • Humans
  • Microbial Sensitivity Tests
  • Mutation
  • Phenotype
  • Pyridines / pharmacology*
  • Pyrones / pharmacology*
  • Sulfonamides

Substances

  • HIV Protease Inhibitors
  • Pyridines
  • Pyrones
  • Sulfonamides
  • HIV Protease
  • tipranavir