Cutting edge: T cells from aged mice are resistant to depletion early during virus infection

被引:27
作者
Jiang, J
Anaraki, F
Blank, KJ
Murasko, DM
机构
[1] Drexel Univ, Coll Med, Dept Microbiol & Immunol, Philadelphia, PA 19129 USA
[2] Drexel Univ, Coll Med, Dept Pathol, Philadelphia, PA 19129 USA
[3] Drexel Univ, Coll Arts & Sci, Dept Biosci & Biotechnol, Philadelphia, PA 19129 USA
关键词
D O I
10.4049/jimmunol.171.7.3353
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aging is associated with decreased expansion of T cells upon stimulation. In young mice, infection induces a transient T cell depletion followed by the development of an Ag-specific T cell response that controls the infection. We found that T cells were depleted early after infection with E55 + murine leukemia retrovirus in young, hut not aged, mice. Adoptive transfer experiments showed donor T cells of young, hut not aged, mice were depleted due to apoptosis in various tissues of young recipients. However, T cells of neither young nor aged donors were depleted in aged recipients. These results indicate that both environmental and intrinsic cellular properties limit depletion of T cells of aged mice and suggest a novel explanation for the decreased T cell response associated with aging.
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页码:3353 / 3357
页数:5
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