The expression of programmed death-1 in circulating CD4+ and CD8+ T cells during hepatitis B virus infection progression and its correlation with clinical baseline characteristics

Gut Liver. 2014 Mar;8(2):186-95. doi: 10.5009/gnl.2014.8.2.186. Epub 2013 Dec 24.

Abstract

Background/aims: Programmed death-1 (PD-1) expression was investigated in CD4(+) and CD8(+) T cells from hepatitis B virus (HBV)-infected patients at the chronic hepatitis B (CHB) infection, liver cirrhosis (LC), and hepatocellular carcinoma (HCC) stages.

Methods: PD-1 expression in circulating CD4(+) and CD8(+) T cells was detected by flow cytometry. The correlations between PD-1 expression and HBV viral load, alanine aminotransaminase (ALT) levels and aspartate aminotransferase (AST) levels were analyzed using GraphPad Prism 5.0.

Results: PD-1 expression in CD4(+) and CD8(+) T cells was significantly increased in both the CHB group and advanced-stage group (LC plus HCC). In the CHB group, PD-1 expression in both CD4(+) and CD8(+) T cells was positively correlated with the HBV viral load, ALT, and AST levels. However, in the LC plus HCC group, significant correlations between PD-1 expression and the clinical parameters were nearly absent.

Conclusions: PD-1 expression in peripheral CD4(+) and CD8(+) T cells is dynamic, changes with HBV infection progression, and is related to HBV viral load and liver function, especially in CHB. PD-1 expression could be utilized as a potential clinical indicator to determine the extent of virus replication and liver injury.

Keywords: Carcinoma, hepatocellular; Hepatitis B virus; Hepatitis B, chronic; Liver cirrhosis; Programmed death-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • CD4-Positive T-Lymphocytes / metabolism*
  • CD8-Positive T-Lymphocytes / metabolism*
  • Carcinoma, Hepatocellular
  • Disease Progression
  • Female
  • Hepatitis B, Chronic / diagnosis*
  • Hepatitis B, Chronic / immunology
  • Humans
  • Liver Cirrhosis
  • Liver Neoplasms
  • Male
  • Programmed Cell Death 1 Receptor / metabolism*
  • Viral Load

Substances

  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor