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首页> 外文期刊>Nature immunology >Cross-priming of CD8~+ T cells stimulated by virus-induced type I interferon
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Cross-priming of CD8~+ T cells stimulated by virus-induced type I interferon

机译:病毒诱导的I型干扰素刺激的CD8〜+ T细胞交叉启动

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摘要

CD8~+ T cell responses can be generated against antigens that are not expressed directly within antigen-presenting cells (APCs), through a process known as cross-priming. To initiate cross-priming, APCs must both capture extracellular antigen and receive specific activation signals. We have investigated the nature of APC activation signals associated with virus infection that stimulate cross-priming. We show that infection with lymphocytic choriomeningitis virus induces cross-priming by a mechanism dependent on type I interferon (IFN-α/β). Activation of cross-priming by IFN-α/β was independent of CD4~+ T cell help or interaction of CD4O and CD4O ligand, and involved direct stimulation of dendritic cells. These data identify expression of IFN-α/β as a mechanism for th induction of cross-priming during virus infections.
机译:通过称为交叉引发的过程,可以针对未在抗原呈递细胞(APC)中直接表达的抗原产生CD8 + T细胞应答。要启动交叉启动,APC必须既捕获细胞外抗原又接收特定的激活信号。我们已经研究了与交叉感染的病毒感染相关的APC激活信号的性质。我们显示淋巴细胞性脉络膜脑膜炎病毒感染可通过依赖于I型干扰素(IFN-α/β)的机制诱导交叉引发。 IFN-α/β的交叉引发激活与CD4〜+ T细胞的帮助或CD4O和CD4O配体的相互作用无关,并且涉及树突状细胞的直接刺激。这些数据确定了IFN-α/β的表达是在病毒感染期间诱导交叉引发的机制。

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