Morphine directs T cells toward T(H2) differentiation

Surgery. 2001 Aug;130(2):304-9. doi: 10.1067/msy.2001.116033.

Abstract

Background: Failure of cell-mediated immunity is thought to increase the morbidity and mortality rates after trauma and major surgical procedures and to be the result, in part, of a redirection of CD4(+) T cells toward T(H2) differentiation. We tested the hypothesis that morphine treatment after injury promotes T(H2) differentiation of precursor T cells through the mu-opioid receptor.

Methods: Human peripheral blood mononuclear cells (PBMCs) or splenocytes from either wild type or mu-opioid receptor knock-out mice were treated in vitro with either vehicle or morphine and then stimulated with anti-CD3/anti-CD28. The supernatant was assayed for T(H1) (interleukin-2 [IL-2], interferon gamma [IFN gamma]) and T(H2) (IL-4, IL-5) cytokines (enzyme-linked immunosorbent assay). Morphine regulation of IL-4 transcription was investigated in PBMCs (IL-4 messenger RNA, nuclear factor of activated T-cells) and Jurkat T cells transfected with a murine IL-4 promoter-luciferase construct. Morphine-induced nuclear factor of activated T-cell (NFAT) binding was assayed with the electromobility shift assay in Jurkat T cells.

Results: Morphine treatment of PBMCs decreases IL-2 and IFN gamma and increases IL-4 and IL-5 as a function of morphine concentration. Morphine treatment in wild type splenocytes inhibited IFN gamma and stimulated IL-4 protein synthesis. Changes in cytokine synthesis were abolished in mu-opioid receptor knockout mice. Morphine treatment increases IL-4 messenger RNA accumulation in PBMCs and increases IL-4 promoter activity in Jurkat T cells. Morphine increases NFAT nuclear protein binding to an NFAT DNA response element.

Conclusions: We conclude that morphine treatment promotes T(H2) differentiation through a mu-opioid receptor mechanism and that morphine treatment increases IL-4 transcription, in part, through an NFAT mechanism.

Publication types

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

MeSH terms

  • Analgesics, Opioid / pharmacology*
  • Animals
  • CD28 Antigens
  • CD3 Complex / immunology
  • Cell Differentiation / drug effects
  • Cell Differentiation / immunology
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-2 / metabolism
  • Interleukin-4 / genetics
  • Interleukin-4 / metabolism
  • Interleukin-5 / metabolism
  • Jurkat Cells
  • Mice
  • Mice, Knockout
  • Morphine / pharmacology*
  • Promoter Regions, Genetic / immunology
  • Receptors, Opioid, mu / genetics
  • Receptors, Opioid, mu / immunology
  • Spleen / cytology
  • Th2 Cells / cytology*
  • Th2 Cells / drug effects*
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / immunology
  • Transfection

Substances

  • Analgesics, Opioid
  • CD28 Antigens
  • CD3 Complex
  • Interleukin-2
  • Interleukin-5
  • Receptors, Opioid, mu
  • Interleukin-4
  • Morphine
  • Interferon-gamma