In vitro phenotypic susceptibility of human immunodeficiency virus type 2 clinical isolates to protease inhibitors

Antimicrob Agents Chemother. 2008 Apr;52(4):1545-8. doi: 10.1128/AAC.01284-07. Epub 2008 Jan 28.

Abstract

We determine phenotypic susceptibility of human immunodeficiency virus type 2 (HIV-2) isolates to amprenavir, atazanavir, darunavir, indinavir, lopinavir, nelfinavir, saquinavir, and tipranavir. Saquinavir, lopinavir, and darunavir are potent against wild-type HIV-2 isolates and should be preferred as first-line options for HIV-2-infected patients. Other protease inhibitors are less active against HIV-2 than against HIV-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Darunavir
  • HIV Protease / drug effects
  • HIV Protease Inhibitors / pharmacology*
  • HIV-2 / classification*
  • HIV-2 / drug effects*
  • HIV-2 / enzymology
  • Humans
  • Inhibitory Concentration 50
  • Lopinavir
  • Microbial Sensitivity Tests
  • Phenotype
  • Pyrimidinones / pharmacology
  • Saquinavir / pharmacology
  • Sulfonamides / pharmacology

Substances

  • HIV Protease Inhibitors
  • Pyrimidinones
  • Sulfonamides
  • Lopinavir
  • HIV Protease
  • Saquinavir
  • Darunavir