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Enteric Virome Sensing—Its Role in Intestinal Homeostasis and Immunity

机译:肠道病毒感测在肠道稳态和免疫中的作用

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摘要

Pattern recognition receptors (PRRs) sensing commensal microorganisms in the intestine induce tightly controlled tonic signaling in the intestinal mucosa, which is required to maintain intestinal barrier integrity and immune homeostasis. At the same time, PRR signaling pathways rapidly trigger the innate immune defense against invasive pathogens in the intestine. Intestinal epithelial cells and mononuclear phagocytes in the intestine and the gut-associated lymphoid tissues are critically involved in sensing components of the microbiome and regulating immune responses in the intestine to sustain immune tolerance against harmless antigens and to prevent inflammation. These processes have been mostly investigated in the context of the bacterial components of the microbiome so far. The impact of viruses residing in the intestine and the virus sensors, which are activated by these enteric viruses, on intestinal homeostasis and inflammation is just beginning to be unraveled. In this review, we will summarize recent findings indicating an important role of the enteric virome for intestinal homeostasis as well as pathology when the immune system fails to control the enteric virome. We will provide an overview of the virus sensors and signaling pathways, operative in the intestine and the mononuclear phagocyte subsets, which can sense viruses and shape the intestinal immune response. We will discuss how these might interact with resident enteric viruses directly or in context with the bacterial microbiome to affect intestinal homeostasis.
机译:模式识别受体(PRR)感测肠道中的共生微生物会在肠粘膜中诱导严格控制的滋补信号,这是维持肠屏障完整性和免疫稳态所必需的。同时,PRR信号通路迅速触发了针对肠道中入侵性病原体的先天免疫防御。肠道和与肠道相关的淋巴组织中的肠道上皮细胞和单核吞噬细胞至关重要地参与了微生物组的传感和调节肠道的免疫反应,以维持对无害抗原的免疫耐受并预防炎症。到目前为止,大多数过程都是在微生物组的细菌成分的背景下进行的。肠道病毒和由这些肠病毒激活的病毒传感器对肠道稳态和炎症的影响才刚刚被弄清楚。在这篇综述中,我们将总结最近的发现,这些发现表明,当免疫系统无法控制肠病毒时,肠病毒对肠道稳态和病理学具有重要作用。我们将概述在肠道和单核吞噬细胞亚群中起作用的病毒传感器和信号传导途径,它们可以感知病毒并影响肠道免疫反应。我们将讨论它们如何与居民肠道病毒直接相互作用或与细菌微生物组相互作用,从而影响肠道稳态。

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