Elevated interleukin-4 expression in severe recurrent hepatitis C virus after liver transplantation

Transplantation. 2007 Apr 15;83(7):906-11. doi: 10.1097/01.tp.0000258729.68871.be.

Abstract

Background: Chronic hepatitis C virus (HCV) is usually associated with high levels of hepatic interleukin (IL)-2 and low levels of IL-4 transcripts. HCV frequently recurs after liver transplantation, and its course is accelerated in this setting. We compared in situ expression of IL-2 and IL-4 in transplanted and nontransplanted patients with HCV.

Methods: A total of 74 liver biopsy specimens were studied; 52 came from transplanted patients, 38 of whom were HCV-positive (17 mild and 21 severe cases of recurrent HCV) and 22 came from nontransplanted patients, 17 of whom were HCV-positive (7 mild and 10 severe cases of HCV). The expression of IL-2 and IL-4 mRNA and IL-4 protein was studied using the reverse transcriptase polymerase chain reaction and immunohistochemical methods, respectively.

Results: IL-2 transcript levels were significantly higher in severe than in mild HCV in both liver graft recipients and nontransplanted patients. However, IL-2 levels were higher in nontransplanted than in transplanted patients. IL-4 transcripts and protein were preferentially detected in graft recipients with severe recurrent HCV.

Conclusion: IL-4 expression is elevated in severe recurrent HCV and may play a role in the progression of hepatic lesions after liver transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Adult
  • Biopsy
  • Cyclosporine / therapeutic use
  • Female
  • Genotype
  • Hepacivirus / genetics
  • Hepatitis C, Chronic / immunology*
  • Hepatitis C, Chronic / pathology
  • Hepatitis C, Chronic / physiopathology
  • Hepatitis C, Chronic / surgery*
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Interleukin-2 / genetics*
  • Interleukin-4 / genetics*
  • Liver Transplantation / immunology*
  • Liver Transplantation / pathology
  • Male
  • Middle Aged
  • RNA, Messenger / genetics
  • Recurrence
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tacrolimus / therapeutic use
  • Transcription, Genetic

Substances

  • Adrenal Cortex Hormones
  • Immunosuppressive Agents
  • Interleukin-2
  • RNA, Messenger
  • Interleukin-4
  • Cyclosporine
  • Tacrolimus