Apoptosis and reduced influenza A virus specific CD8+ T cells in aging mice

Cell Death Differ. 2002 Jun;9(6):651-60. doi: 10.1038/sj.cdd.4401011.

Abstract

Some studies have reported increased apoptosis in CD8(+) T cells from aged mice. We previously demonstrated diminished virus-specific CD8(+) cytotoxic T lymphocyte (CTL) activity in aged mice in comparison to young mice. The present study investigated the role of apoptosis in age-related influenza virus-specific CD8(+) CTL deficiency. Splenocytes from influenza-primed aged and young mice were stimulated in vitro with virus. The CD8(+) T cell/total lymphocyte ratios correlated with CTL activity and were significantly decreased and increased in aged and young mice, respectively. Fas, FasL, TNF-alpha and TNFR-p55 expression, measured by flow cytometry, ELISA and/or RT-PCR, were significantly elevated in aged mice. Apoptotic CD8(+) T cells (Annexin V binding) were also elevated in aged mice. IL-12 treatment increased CD8(+) CTL activity and IFN-gamma production but did not affect apoptosis. Thus, apoptosis may contribute to reduced influenza virus-specific CD8(+) T cell frequency, CTL deficiency and increased influenza disease in aging.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adjuvants, Immunologic / pharmacology
  • Aging / immunology*
  • Aging / physiology
  • Animals
  • Apoptosis*
  • Fas Ligand Protein
  • Immunologic Memory
  • Influenza A virus / immunology*
  • Interferon-gamma / metabolism
  • Interleukin-12 / pharmacology
  • Membrane Glycoproteins / metabolism
  • Mice
  • T-Lymphocytes, Cytotoxic / immunology*
  • fas Receptor / metabolism

Substances

  • Adjuvants, Immunologic
  • Fas Ligand Protein
  • Fasl protein, mouse
  • Membrane Glycoproteins
  • fas Receptor
  • Interleukin-12
  • Interferon-gamma