Study of liver-targeted regulatory T cells in hepatitis B and C virus in chronically infected patients

Liver Int. 2009 May;29(5):702-7. doi: 10.1111/j.1478-3231.2008.01842.x. Epub 2008 Jul 30.

Abstract

Introduction: Regulatory T cells (Tregs) play a critical role in chronic viral infections. The role of Tregs in chronic hepatitis B (CHB) and chronic hepatitis C (CHC) is unknown. This study examined the distribution and frequency of forkhead box p3(+) (Foxp3(+)) Tregs in the liver tissue and compared the clinicopathological characteristics of CHB and CHC patients.

Methods: Liver needle biopsies were obtained from 26 patients who were hepatitis B surface antigen positive and 27 patients who were hepatitis C virus antibody positive.

Results: The ratio of Foxp3(+) Tregs in CD3(+) T cells was similar in HBV and in HCV cases. In HBV cases, the variables that were positively associated with the ratio of Foxp3(+) Tregs in CD3(+) T cells included the serum alanine aminotransferase level (R=0.402, P=0.025) and the ratio of CD8(+) T cell plus CD56(+) NK cell against CD4(+) T cell (R=0.53, P=0.005). The ratio of Foxp3(+) Tregs in CD3(+) T cells increased more in the severe activity group than in the mild activity group (P=0.04). In HCV cases, the ratio of Foxp3(+) Tregs in CD3(+) T cells increased significantly in terms of the genotype2 (P=0.0002) and male gender (P=0.04). In addition, the ratio of Foxp3(+) Tregs in CD3(+) T cells showed a negative correlation with the ratio of CD8(+) T cell plus CD56(+) NK cell against CD4(+) T cell (R=-0.508, P=0.005) and HCV viral load (R=-0.482, P=0.001).

Conclusions: Liver-targeted regulatory T cells present similarly in CHB and CHC, but their relationship with the effector cell population, the inflammation grade or the viral load is different between CHB and CHC.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Alanine Transaminase / blood
  • CD8-Positive T-Lymphocytes / immunology
  • Female
  • Forkhead Transcription Factors / metabolism*
  • Hepatitis B / immunology*
  • Hepatitis C / immunology*
  • Hepatocytes / immunology*
  • Humans
  • Male
  • Middle Aged
  • Statistics, Nonparametric
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Alanine Transaminase