首页> 外文期刊>Journal of Virology >Splenic priming of virus-specific CD8 T cells following influenza virus infection.
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Splenic priming of virus-specific CD8 T cells following influenza virus infection.

机译:脾的启动病毒特异性CD8 T细胞在流感病毒感染。

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In healthy individuals, influenza virus (IAV) infection generally remains localized to the epithelial cells of the respiratory tract. Previously, IAV-specific effector CD8 T cells found systemically during the course of IAV infection were thought to have been primed in lung-draining lymph nodes with subsequent migration to other tissues. However, little is known about whether other lymphoid sites participate in the generation of virus-specific CD8 T cells during localized IAV infection. Here, we present evidence of early CD8 T cell priming in the spleen following respiratory IAV infection independent of lung-draining lymph node priming of T cells. Although we found early indications of CD8 T cell activation in the lymph nodes draining the respiratory tract, we also saw evidence of virus-specific CD8 T cell activation in the spleen. Furthermore, CD8 T cells primed in the spleen differentiated into memory cells of equivalent longevity and with similar recall capacity as CD8 T cells primed in the draining lymph nodes. These data showed that the spleen contributes to the virus-specific effector and memory CD8 T cell populations that are generated in response to respiratory infection.
机译:在健康个体,流感病毒(IAV)感染通常仍然是局部的呼吸道上皮细胞。此前,IAV-specific效应CD8 T细胞发现系统IAV的过程中感染被认为已经启动与后续lung-draining淋巴结迁移到其他组织。知道是否其他淋巴网站参与代的特异性CD8 T细胞在局部IAV感染。我们提出早期CD8 T细胞启动的证据在呼吸后的脾IAV感染独立于lung-draining淋巴结启动的T细胞。CD8 T细胞激活的淋巴结导致呼吸道,我们也看到了病毒特异性CD8 T细胞激活的证据在脾。脾细胞分化成记忆等效寿命和类似的召回CD8 T细胞启动的排水能力淋巴结。有助于特异效应和CD8记忆T细胞数量生成对呼吸道感染的反应。

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