Department of Surgery and Immunobiology and Transplant Science Center, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, 130021, China.
Cell Mol Life Sci. 2022 May 23;79(6):313. doi: 10.1007/s00018-022-04332-z.
Gastroenteritis is inflammation of the lining of stomach and intestines and causes significant morbidity and mortality worldwide. Many viruses, especially RNA viruses are the most common cause of enteritis. Innate immunity is the first line of host defense against enteric RNA viruses and virus-induced intestinal inflammation. The first layer of defense against enteric RNA viruses in the intestinal tract is intestinal epithelial cells (IECs), dendritic cells and macrophages under the intestinal epithelium. These innate immune cells express pathogen-recognition receptors (PRRs) for recognizing enteric RNA viruses through sensing viral pathogen-associated molecular patterns (PAMPs). As a result of this recognition type I interferon (IFN), type III IFN and inflammasome activation occurs, which function cooperatively to clear infection and reduce viral-induced intestinal inflammation. In this review, we summarize recent findings about mechanisms involved in enteric RNA virus-induced intestinal inflammation. We will provide an overview of the enteric RNA viruses, their RNA sensing mechanisms by host PRRs, and signaling pathways triggered by host PRRs, which shape the intestinal immune response to maintain intestinal homeostasis.
肠胃炎是胃和肠道内层的炎症,会在全球范围内导致很高的发病率和死亡率。许多病毒,尤其是 RNA 病毒,是肠胃炎的最常见病因。先天免疫是宿主防御肠道 RNA 病毒和病毒诱导的肠道炎症的第一道防线。肠道中针对肠道 RNA 病毒的第一道防线是肠道上皮细胞 (IECs)、上皮下的树突状细胞和巨噬细胞。这些先天免疫细胞通过感知病毒病原体相关分子模式 (PAMPs) 表达识别肠道 RNA 病毒的病原体识别受体 (PRRs)。作为这种识别的结果,I 型干扰素 (IFN)、III 型 IFN 和炎性小体激活发生,它们协同作用以清除感染并减少病毒诱导的肠道炎症。在这篇综述中,我们总结了肠道 RNA 病毒诱导的肠道炎症涉及的机制的最新发现。我们将概述肠道 RNA 病毒及其宿主 PRRs 对 RNA 的感知机制,以及宿主 PRRs 触发的信号通路,这些机制塑造了肠道对维持肠道内稳态的免疫反应。