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CD8 T-cell memory differentiation during acute and chronic viral infections.

机译:急性和慢性病毒感染期间的CD8 T细胞记忆分化。

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摘要

CD8 T cell responses play an important role in protection against intracellular parhogens. Memory CD8 T cells mediate rapid clearance of pathogens upon secondary infection owing to their elevated frequency, ready localization to peripheral sites of infection and their ability to rapidly expand and mount effector functions. Such potent long-lasting protective memory CD8 T cells develop in acute infections where antigen is effectively cleared. In contrast, chronic infections with persistently high viral loads are characterized by CD8 T-cell dysfunction. In this chapter we present our current understanding of signals and mechanisms that regulate the development of functional long-lived memory CD8 T cells during acute infections. This is discussed in the context of proposed models of memory differentiation and compared with CD8 T-cell exhaustion and altered T-cell homeostasis, as occurs during persistent viral infections.
机译:CD8 T细胞反应在针对细胞内致癌物的保护中起重要作用。记忆CD8 T细胞由于其频率升高,易于定位到感染的周围部位以及其迅速扩展和发挥效应子功能的能力,因此在继发感染时介导了病原体的快速清除。这种有效的持久性保护性记忆CD8 T细胞会在急性感染中发展,其中抗原被有效清除。相反,具有持续高病毒载量的慢性感染的特征是CD8 T细胞功能障碍。在本章中,我们介绍了我们目前对信号和机制的理解,这些信号和机制可调节急性感染期间功能性长寿记忆CD8 T细胞的发育。这在提出的记忆分化模型中进行了讨论,并与CD8 T细胞耗竭和改变的T细胞动态平衡进行了比较(如在持续性病毒感染期间发生的情况)。

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