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

被引:0
作者
Y Zhang
Y Wang
X Gilmore
K Xu
M Chen
P Tebebi
I N Mbawuike
机构
[1] Influenza Research Center,Department of Molecular Virology and Microbiology
[2] Respiratory Pathogens Research Unit,undefined
[3] Baylor College of Medicine,undefined
来源
Cell Death & Differentiation | 2002年 / 9卷
关键词
aging; apoptosis; influenza virus; CD8; T cells;
D O I
暂无
中图分类号
学科分类号
摘要
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-α 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-γ 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.
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页码:651 / 660
页数:9
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