Biliary obstruction results in PD-1-dependent liver T cell dysfunction and acute inflammation mediated by Th17 cells and neutrophils

J Leukoc Biol. 2013 Oct;94(4):813-23. doi: 10.1189/jlb.0313137. Epub 2013 Jul 24.

Abstract

Biliary obstruction is a common clinical problem that is associated with intrahepatic inflammation and impaired immunity. PD-1 is well known to mediate T cell dysfunction but has been reported to promote and attenuate acute inflammation in various injury models. With the use of a well-established murine model of BDL, we studied the effects of intrahepatic PD-1 expression on LTC function, inflammation, and cholestasis. Following BDL, PD-1 expression increased significantly among LTCs. Increased PD-1 expression following BDL was associated with decreased LTC proliferation and less IFN-γ production. Elimination of PD-1 expression resulted in significantly improved proliferative capacity among LTC following BDL, in addition to a more immunostimulatory cytokine profile. Not only was LTC function rescued in PD-1(-/-) mice, but also, the degrees of biliary cell injury, cholestasis, and inflammation were diminished significantly compared with WT animals following BDL. PD-1-mediated acute inflammation following BDL was associated with expansions of intrahepatic neutrophil and Th17 cell populations, with the latter dependent on IL-6. PD-1 blockade represents an attractive strategy for reversing intrahepatic immunosuppression while limiting inflammatory liver damage.

Keywords: Treg; intrahepatic immunity; obstructive jaundice.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bile Ducts / metabolism
  • Bile Ducts / pathology
  • Cell Proliferation
  • Cholestasis / complications
  • Cholestasis / immunology*
  • Cholestasis / pathology
  • Cholestasis / physiopathology*
  • Inflammation / complications
  • Inflammation / immunology*
  • Inflammation / pathology
  • Interleukin-6 / metabolism
  • Jaundice / complications
  • Jaundice / immunology
  • Jaundice / pathology
  • Jaundice / physiopathology
  • Ligation
  • Liver / immunology
  • Liver / pathology*
  • Liver / physiopathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Neutrophils / immunology
  • Neutrophils / pathology*
  • Programmed Cell Death 1 Receptor / metabolism*
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology
  • Th17 Cells / immunology
  • Th17 Cells / pathology*
  • Up-Regulation

Substances

  • Interleukin-6
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor