Toll-like receptor 3 and 7/8 function is impaired in hepatitis C rapid fibrosis progression post-liver transplantation

Am J Transplant. 2013 Apr;13(4):943-953. doi: 10.1111/ajt.12165. Epub 2013 Feb 20.

Abstract

Recurrence of hepatitis C (HCV) postliver transplant is universal, with a subgroup developing rapid hepatic fibrosis. Toll-like receptors (TLRs) are critical to innate antiviral responses and HCV alters TLR function to evade immune clearance. Whether TLRs play a role in rapid HCV recurrence posttransplant is unknown. We stimulated peripheral blood mononuclear cells (PBMCs) from 70 patients with HCV postliver transplant with TLR subclass-specific ligands and measured cytokine production, TLR expression and NK cell function. Rate of fibrosis progression was calculated using posttransplant liver biopsies graded by Metavir scoring (F0-4; R=fibrosis stage/year posttransplant; rapid fibrosis defined as >0.4 units/year). Thirty of 70 (43%) patients had rapid fibrosis progression. PBMCs from HCV rapid-fibrosers produced less IFNα with TLR7/8 stimulation (p=0.039), less IL-6 at baseline (p=0.027) and with TLR3 stimulation (p=0.008) and had lower TLR3-mediated monocyte IL-6 production (p=0.028) compared with HCV slow fibrosers. TLR7/8-mediated NKCD56 dim cell secretion of IFNγ was impaired in HCV rapid fibrosis (p=0.006) independently of IFNα secretion and TLR7/8 expression, while cytotoxicity remained preserved. Impaired TLR3 and TLR7/8-mediated cytokine responses may contribute to aggressive HCV recurrence postliver transplantation through impaired immune control of HCV and subsequent activation of fibrogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cross-Sectional Studies
  • Cytokines / metabolism
  • Disease Progression
  • Female
  • Hepacivirus
  • Hepatitis C / metabolism
  • Hepatitis C / physiopathology*
  • Humans
  • Interferon-alpha / metabolism
  • Interferon-gamma / metabolism
  • Interleukin-6 / metabolism
  • Killer Cells, Natural / cytology
  • Leukocytes, Mononuclear / cytology
  • Ligands
  • Liver Cirrhosis / physiopathology
  • Liver Cirrhosis / virology
  • Liver Failure / therapy
  • Liver Transplantation*
  • Male
  • Middle Aged
  • Prospective Studies
  • Recurrence
  • Toll-Like Receptor 3 / metabolism*
  • Toll-Like Receptor 7 / metabolism*
  • Toll-Like Receptor 8 / metabolism*

Substances

  • Cytokines
  • Interferon-alpha
  • Interleukin-6
  • Ligands
  • TLR3 protein, human
  • TLR7 protein, human
  • TLR8 protein, human
  • Toll-Like Receptor 3
  • Toll-Like Receptor 7
  • Toll-Like Receptor 8
  • Interferon-gamma