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IL-21 Deficiency Influences CD8 T Cell Quality and Recall Responses following an Acute Viral Infection

机译:IL-21缺乏影响急性病毒感染后CD8 T细胞质量和召回反应。

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CD4 T cells are principal producers of IL-21 and are often required for optimal CD8 T cell responses. Therefore, we investigated the importance of IL-21 in determining the phenotypic attributes, functional quality, and maintenance of antiviral CD8 T cells following acute infection with the prototypic mouse pathogen lymphocytic choriomeningitis virus. Previous reports have documented an obligatory role for IL-21 in sustaining CD8 T cell responses during chronic infections. Here we show that the requirements for IL-21 are less stringent following acute infections; however, in the absence of IL-21, the capacity of CD8 T cells to attain the polyfunctional trait of IL-2 production is consistently reduced during both the effector and memory phases. This is further supported by in vitro studies showing that the addition of IL-21 promotes the differentiation of IL-2–producing CD8 T cells. Although the generation of memory CD8 T cells, which are capable of mounting protective recall responses, proceeds independently of IL-21, we demonstrate that IL-21 does function to support secondary responses, especially under competitive conditions. Collectively, these studies highlight the potential roles of IL-21 in determining the quality of CD8 T cell responses postinfection.
机译:CD4 T细胞是IL-21的主要产生者,通常是最佳CD8 T细胞反应所必需的。因此,我们调查了IL-21在确定原型小鼠病原体淋巴细胞性脉络膜脑膜炎病毒急性感染后确定表型属性,功能质量和维持抗病毒CD8 T细胞中的重要性。先前的报道已证明IL-21在慢性感染期间在维持CD8 T细胞应答中的强制性作用。在这里,我们表明急性感染后对IL-21的要求不那么严格。然而,在没有IL-21的情况下,在效应期和记忆期两者中,CD8T细胞获得IL-2产生的多功能性的能力不断降低。体外研究进一步证明了这一点,研究表明添加IL-21可以促进产生IL-2的CD8 T细胞的分化。尽管能够安装保护性召回反应的记忆CD8 T细胞的产生独立于IL-21进行,但我们证明IL-21确实起着支持次级反应的作用,尤其是在竞争条件下。这些研究共同强调了IL-21在确定感染后CD8 T细胞反应质量方面的潜在作用。

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