Methylnaltrexone antagonizes opioid-mediated enhancement of HIV infection of human blood mononuclear phagocytes

J Pharmacol Exp Ther. 2003 Dec;307(3):1158-62. doi: 10.1124/jpet.103.056697. Epub 2003 Oct 14.

Abstract

Opioid abuse has been postulated as a cofactor in the immunopathogenesis of human immunodeficiency virus (HIV) infection and AIDS. We and others have recently demonstrated that opioid enhances HIV infection of human macrophages through modulation of beta-chemokines and the CCR5 receptor and that this effect is reversed by naltrexone, a tertiary opioid antagonist. Tertiary opioid antagonists cannot be used in opioid-dependent patients because they precipitate withdrawal or reversal of analgesia. We determined whether the quaternary opioid antagonist methylnaltrexone (MNTX), now in phase III clinical trials for opioid-induced constipation, reverses the opioid-mediated enhancement of HIV infection of macrophages at clinically relevant doses. MNTX completely abrogated morphine-induced HIV Bal strain infection of macrophages. MNTX also inhibited the R5 strain (ADA) envelope-pseudotyped HIV replication induced by morphine. Furthermore, MNTX abolished morphine-mediated up-regulation of CCR5 receptor expression. The ability of MNTX to block opioid-induced CCR5 expression and HIV replication at clinically relevant doses may have additional benefit for opioid abusers with HIV infection, or patients with AIDS pain receiving opioids.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cells, Cultured
  • HIV Infections / prevention & control*
  • HIV Reverse Transcriptase / metabolism
  • Humans
  • Monocytes / drug effects
  • Monocytes / virology*
  • Morphine / pharmacology
  • Naltrexone / analogs & derivatives*
  • Naltrexone / pharmacology*
  • Narcotic Antagonists / pharmacology*
  • Narcotics / pharmacology*
  • Quaternary Ammonium Compounds
  • Receptors, CCR5 / biosynthesis

Substances

  • Narcotic Antagonists
  • Narcotics
  • Quaternary Ammonium Compounds
  • Receptors, CCR5
  • methylnaltrexone
  • Naltrexone
  • Morphine
  • HIV Reverse Transcriptase