Dynamic decrease in PD-1 expression correlates with HBV-specific memory CD8 T-cell development in acute self-limited hepatitis B patients

J Hepatol. 2009 Jun;50(6):1163-73. doi: 10.1016/j.jhep.2009.01.026. Epub 2009 Mar 29.

Abstract

Background/aims: Programmed death-1 (PD-1) upregulation can impair virus-specific CD8 T-cell responses during chronic viral infection. Whether and how PD-1 affects virus-specific memory CD8 T cells in humans with acute viral infection, however, remains largely undefined.

Methods: The association between PD-1 expression and HBV-specific memory CD8 T-cell responses were longitudinally analyzed in eighteen patients with acute hepatitis B virus (HBV) infection, including ten patients with human leucocyte antigen (HLA)-A201 and eight with other HLA-A2 subtypes.

Results: At clinical onset, PD-1 was significantly up-regulated and subsequently led to the functional suppression of HBV-specific effector CD8 T cells, as blocking PD-1/PD-L1 interactions in vitro enhanced their proliferation and IFN-gamma production. Following disease resolution, HBV-specific effector CD8 T cells developed into memory T cells. During this period, the dynamic PD-1 decrease was numerically correlated with the reduction of HBV-specific CD8 T-cell frequency, phenotypically with an acquisition of CCR7, CD45RA and CD127 expressions, and functionally with the increase in proliferation and IFN-gamma production of the memory T cells.

Conclusions: PD-1-mediated inhibitory signaling not only attenuates HBV-specific CD8 T-cell effector function during the acute phase of infection but also correlates with the development of HBV-specific memory CD8 T cells following disease resolution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adult
  • Antigens, CD / genetics*
  • Antigens, CD / immunology*
  • Antigens, Viral / genetics
  • Apoptosis Regulatory Proteins / genetics*
  • Apoptosis Regulatory Proteins / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / virology*
  • Cell Proliferation
  • Epitopes / genetics
  • Female
  • Gene Expression
  • HLA-A Antigens / genetics
  • HLA-A2 Antigen / genetics
  • Hepatitis B / immunology*
  • Hepatitis B / virology
  • Hepatitis B virus / genetics
  • Hepatitis B virus / immunology*
  • Humans
  • Immunologic Memory
  • In Vitro Techniques
  • Interferon-gamma / biosynthesis
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Models, Biological
  • Programmed Cell Death 1 Receptor
  • Young Adult

Substances

  • Antigens, CD
  • Antigens, Viral
  • Apoptosis Regulatory Proteins
  • Epitopes
  • HLA-A Antigens
  • HLA-A*02:01 antigen
  • HLA-A2 Antigen
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Interferon-gamma