Department of Microbiology, Faculty of Medicine, Shimane University, Shimane, Japan.
Front Immunol. 2020 Mar 3;11:367. doi: 10.3389/fimmu.2020.00367. eCollection 2020.
Epstein-Barr virus (EBV) is an oncogenic human herpes virus that was discovered in 1964. Viral non-coding RNAs, such as HI-A rightward fragment-derived microRNAs (BART miRNAs) or HI-H rightward fragment 1-derived miRNAs (BHRF1 miRNA) in EBV-infected cells have been recently reported. Host miRNAs are also upregulated upon EBV infection. Viral and host miRNAs are important in maintaining viral infection and evasion of host immunity. Although miRNAs in EBV-infected cells often promote cell proliferation by targeting apoptosis or cell cycle, this review focuses on the regulation of the recognition of the host immune system. This review firstly describes the location and organization of two clusters of viral miRNAs, then describes evasion from host immune surveillance systems by modulating viral gene expression or inhibiting innate and acquired immunity by viral miRNAs as well as host miRNAs. Another topic is the enigmatic depletion of viral miRNAs in several types of EBV-infected tumor cells. Finally, this review introduces the strong correlation of nasopharyngeal cancer cases with a newly identified single nucleotide polymorphism that enhances BART miRNA promoter activity.
EB 病毒(EBV)是一种致癌的人类疱疹病毒,于 1964 年被发现。最近有报道称,在 EBV 感染的细胞中存在病毒非编码 RNA,如 HI-A 右向片段衍生的 microRNAs(BART miRNAs)或 HI-H 右向片段 1 衍生的 miRNAs(BHRF1 miRNA)。宿主 microRNAs 也在 EBV 感染后上调。病毒和宿主 microRNAs 在维持病毒感染和逃避宿主免疫方面发挥着重要作用。尽管 EBV 感染细胞中的 microRNAs 通常通过靶向细胞凋亡或细胞周期来促进细胞增殖,但本综述重点关注宿主免疫系统识别的调节。本文首先描述了两个病毒 microRNA 簇的位置和组织,然后描述了通过调节病毒基因表达或通过病毒 microRNAs 和宿主 microRNAs 抑制先天和获得性免疫来逃避宿主免疫监视系统。另一个主题是几种 EBV 感染的肿瘤细胞中神秘的病毒 microRNAs 耗竭。最后,本综述介绍了与新发现的增强 BART miRNA 启动子活性的单核苷酸多态性强烈相关的鼻咽癌病例。