Increased expression of interleukin-4 during liver allograft rejection

J Hepatol. 1999 May;30(5):935-43. doi: 10.1016/s0168-8278(99)80150-0.

Abstract

Background/aims: To investigate the respective roles of interleukin-2 (IL-2) and IL-4 during rejection, we evaluated the expression of IL-2, IL-2 receptor and IL-4 in human liver allografts.

Methods: Immunohistochemistry and RT-PCR were performed in liver biopsies. To determine the effects of immunosuppression and cholestasis in IL-4 production, in vitro experiments were also designed.

Results: IL-2 protein and its mRNA were absent in the liver, with minimal expression of IL-2 receptor, during rejection. In contrast, IL-4 protein and its mRNA were highly expressed during acute and chronic rejection, whereas this expression was absent in stable liver transplant recipients. In vitro, cyclosporine potently inhibited IL-2 and IL-2 receptor expression of activated mononuclear blood cells, but poorly inhibited IL-4 expression. Chenodeoxycholic acid decreased IL-2 and IL-2 receptor expression, but increased IL-4 expression.

Conclusions: During liver allograft rejection, IL-2 pathway is down-regulated, while IL-4 expression is increased by cholestasis and poorly inhibited by cyclosporine. These data suggest that IL-4 is involved in the mechanisms of liver allograft rejection in patients treated with cyclosporine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adult
  • Cholestasis
  • Chronic Disease
  • Cyclosporine / pharmacology
  • Female
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology
  • Graft Rejection / immunology*
  • Graft Rejection / pathology
  • Humans
  • Immunohistochemistry
  • Immunosuppression Therapy
  • Interleukin-2 / analysis
  • Interleukin-2 / genetics
  • Interleukin-4 / analysis
  • Interleukin-4 / genetics*
  • Liver Transplantation / immunology*
  • Liver Transplantation / pathology*
  • Male
  • Middle Aged
  • Postoperative Complications / immunology
  • Postoperative Complications / pathology
  • RNA, Messenger / analysis
  • Receptors, Interleukin-2 / analysis
  • Receptors, Interleukin-2 / genetics
  • Retrospective Studies
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription, Genetic
  • Transplantation, Homologous

Substances

  • Interleukin-2
  • RNA, Messenger
  • Receptors, Interleukin-2
  • Interleukin-4
  • Cyclosporine