CCR5 antagonism in HIV infection: current concepts and future opportunities

Annu Rev Med. 2012:63:81-93. doi: 10.1146/annurev-med-052010-145454. Epub 2011 Oct 27.

Abstract

CCR5 antagonists inhibit HIV-1 entry by blocking the interaction of HIV-1 with the CCR5 cellular receptor. In patients with established HIV-1 infection, some viral strains use an alternative coreceptor for HIV-1 entry, CXCR4; CCR5 antagonists are not effective in patients harboring these viral strains. Coreceptor tropism testing of viral strains in an individual patient is necessary prior to treating with a CCR5 antagonist. There is one CCR5 antagonist, maraviroc, that is FDA-approved for treatment of HIV-1 infection. This drug is used most commonly for the treatment of HIV-1 infection in patients who have failed other antiretroviral regimens. In addition to virologic effects, CCR5 antagonists are under investigation for immune-modulating effects and for HIV-1 prevention. Ongoing research will further elucidate the role of CCR5 antagonists in combating HIV disease.

Publication types

  • Review

MeSH terms

  • CCR5 Receptor Antagonists*
  • Cyclohexanes / therapeutic use*
  • Drug Discovery / trends
  • HIV Fusion Inhibitors / therapeutic use
  • HIV Infections / prevention & control*
  • HIV Infections / virology*
  • HIV-1 / metabolism*
  • Humans
  • Maraviroc
  • Receptors, CCR5 / metabolism
  • Triazoles / therapeutic use*

Substances

  • CCR5 Receptor Antagonists
  • Cyclohexanes
  • HIV Fusion Inhibitors
  • Receptors, CCR5
  • Triazoles
  • Maraviroc