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首页> 外文期刊>Mechanisms of Ageing and Development >Enhancement of virus-specific expansion of transgenic CD8 T cells in aged mice by dendritic cells.
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Enhancement of virus-specific expansion of transgenic CD8 T cells in aged mice by dendritic cells.

机译:树突状细胞增强老年小鼠转基因CD8 T细胞的病毒特异性扩增。

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摘要

Aging is associated with a decreased CD8 T cell response to multiple antigens and to virus infection. Although both intrinsic and extrinsic factors have been shown to contribute to the decrease, the mechanisms are still largely unknown. In this study, the role of dendritic cells (DCs) in the age-associated decrease was examined. Influenza-specific TCR transgenic CD8 T cells of young mice demonstrated limited expansion in response to influenza infection when adoptively transferred to aged compared to young mice. This decreased response in aged mice could be significantly enhanced when DCs of young mice were co-transferred. Co-transfer of DCs had no impact in young recipient mice. Adoptive transfer of the DCs also increased the endogenous CD8 T cell response of intact aged mice, although to a lesser degree. These results suggest that the diminished CD8 T cell response to virus infection in aged mice is partially attributable to age-associated changes in DCs.
机译:衰老与对多种抗原和病毒感染的CD8 T细胞应答降低有关。尽管已显示出内在和外在因素均对这种下降有贡献,但其机理仍是未知之数。在这项研究中,研究了树突状细胞(DC)在与年龄相关的减少中的作用。与年幼小鼠相比,年幼小鼠的流感特异性TCR转基因CD8 T细胞在过继转移至老年时表现出对流感感染的有限扩展。当年轻小鼠的DC共转移时,老年小鼠中这种降低的反应可以得到显着增强。 DC的共转移对年轻的受体小鼠没有影响。 DC的过继转移也增加了完整衰老小鼠的内源性CD8 T细胞应答,尽管程度较小。这些结果表明,衰老小鼠中对病毒感染的CD8 T细胞应答减弱部分归因于DC的年龄相关变化。

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