HIV-1 integrase inhibitor resistance and its clinical implications

J Infect Dis. 2011 May 1;203(9):1204-14. doi: 10.1093/infdis/jir025.

Abstract

With the approval in 2007 of the first integrase inhibitor (INI), raltegravir, clinicians became better able to suppress virus replication in patients infected with human immunodeficiency virus type 1 (HIV-1) who were harboring many of the most highly drug-resistant viruses. Raltegravir also provided clinicians with additional options for first-line therapy and for the simplification of regimens in patients with stable virological suppression. Two additional INIs in advanced clinical development-elvitegravir and S/GSK1349572-may prove equally versatile. However, the INIs have a relatively low genetic barrier to resistance in that 1 or 2 mutations are capable of causing marked reductions in susceptibility to raltegravir and elvitegravir, the most well-studied INIs. This perspective reviews the genetic mechanisms of INI resistance and their implications for initial INI therapy, the treatment of antiretroviral-experienced patients, and regimen simplification.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anti-HIV Agents / pharmacology*
  • Anti-HIV Agents / therapeutic use
  • Drug Resistance, Viral*
  • HIV Infections / drug therapy*
  • HIV Infections / virology*
  • HIV Integrase / genetics*
  • HIV Integrase / metabolism
  • HIV-1 / drug effects*
  • HIV-1 / isolation & purification
  • Humans
  • Mutant Proteins / genetics
  • Mutant Proteins / metabolism
  • Pyrrolidinones / pharmacology*
  • Pyrrolidinones / therapeutic use
  • Raltegravir Potassium

Substances

  • Anti-HIV Agents
  • Mutant Proteins
  • Pyrrolidinones
  • Raltegravir Potassium
  • HIV Integrase
  • p31 integrase protein, Human immunodeficiency virus 1