Expression of the DX5 antigen on CD8+ T cells is associated with activation and subsequent cell death or memory during influenza virus infection

被引:0
作者
Kambayashi, T
Assarsson, E
Chambers, BJ
Ljunggren, HG [1 ]
机构
[1] Karolinska Inst, Ctr Microbiol & Tumor Biol, S-17177 Stockholm, Sweden
[2] Huddinge Univ Hosp, Karolinska Inst, Dept Med, Ctr Infect Med, Stockholm, Sweden
关键词
CD8(+) T cell; NK cell; apoptosis; viral infection; memory;
D O I
10.1002/1521-4141(200105)31:5<1523::AID-IMMU1523>3.0.CO;2-S
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The antigen recognized by the DX5 antibody (DX5 antigen) is expressed on all murine NK cells. In the present study we found that a proportion of CD8(+) T cells (similar to5%) also express the DX5 antigen in uninfected mice, and that numbers of CD8(+) T cells expressing DX5 are significantly higher in the lungs of influenza virus-infected mice representing up to 50% of all CD8(+) T cells on day 10 post infection. The expression of the DX5 antigen on CD8(+) T cells was associated with a memory phenotype in uninfected C57BL/6 mice and with an activation phenotype during influenza virus infection. Interestingly, when lymphocytes were isolated from lungs of influenza virus-infected mice on day 10 post infection and adoptively transferred into recombination activating gene-1 (RAG1)-deficient mice, CD8(+)DX5(+) cells could not be recovered from the recipient mice 2 days later. Moreover, CD8(+)DX5(+) cells were not detected when lung cells were removed from day 10 influenza virus-infected mice and cultured in vitro for 2 days. However, CD8(+)DX5(+) cells could be detected when apoptosis inhibitors were added to these cultures, suggesting that the CD8(+)DX5(+) cells underwent apoptosis during cell culture. Furthermore, almost all DX5 expressing CD8(+) cells from lungs of mice on day 10 post influenza virus infection stained positively with Annexin-V. Taken together, the data suggest that CD8(+) T cells expressing DX5 are associated with an activation/memory phenotype and are biased towards apoptosis.
引用
收藏
页码:1523 / 1530
页数:8
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