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系统生物学揭示了干扰素对呼吸道病毒感染的反应。

Systems biology unravels interferon responses to respiratory virus infections.

作者信息

Kroeker Andrea L, Coombs Kevin M

机构信息

Andrea L Kroeker, Department of Physiology, University of Manitoba, Winnipeg, MB R3E 0J9, Canada.

出版信息

World J Biol Chem. 2014 Feb 26;5(1):12-25. doi: 10.4331/wjbc.v5.i1.12.

DOI:10.4331/wjbc.v5.i1.12
PMID:24600511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3942539/
Abstract

Interferon production is an important defence against viral replication and its activation is an attractive therapeutic target. However, it has long been known that viruses perpetually evolve a multitude of strategies to evade these host immune responses. In recent years there has been an explosion of information on virus-induced alterations of the host immune response that have resulted from data-rich omics technologies. Unravelling how these systems interact and determining the overall outcome of the host response to viral infection will play an important role in future treatment and vaccine development. In this review we focus primarily on the interferon pathway and its regulation as well as mechanisms by which respiratory RNA viruses interfere with its signalling capacity.

摘要

干扰素的产生是抵御病毒复制的重要防御机制,其激活是一个有吸引力的治疗靶点。然而,长期以来人们都知道病毒会不断进化出多种策略来逃避这些宿主免疫反应。近年来,由于数据丰富的组学技术,关于病毒诱导的宿主免疫反应改变的信息呈爆炸式增长。弄清楚这些系统如何相互作用以及确定宿主对病毒感染反应的总体结果,将在未来的治疗和疫苗开发中发挥重要作用。在这篇综述中,我们主要关注干扰素途径及其调节,以及呼吸道RNA病毒干扰其信号传导能力的机制。

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本文引用的文献

1
ISG15 regulates peritoneal macrophages functionality against viral infection.ISG15 调节腹膜巨噬细胞对抗病毒感染的功能。
PLoS Pathog. 2013;9(10):e1003632. doi: 10.1371/journal.ppat.1003632. Epub 2013 Oct 10.
2
Rhinovirus-induced interferon production is not deficient in well controlled asthma.鼻病毒诱导的干扰素产生在良好控制的哮喘中并不缺乏。
Thorax. 2014 Mar;69(3):240-6. doi: 10.1136/thoraxjnl-2012-202909. Epub 2013 Oct 14.
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microRNAs in circulation are altered in response to influenza A virus infection in humans.循环中的 microRNAs 会因人类感染甲型流感病毒而发生改变。
PLoS One. 2013 Oct 7;8(10):e76811. doi: 10.1371/journal.pone.0076811. eCollection 2013.
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Small RNA profiling of influenza A virus-infected cells identifies miR-449b as a regulator of histone deacetylase 1 and interferon beta.流感 A 病毒感染细胞的小 RNA 谱分析鉴定 miR-449b 为组蛋白去乙酰化酶 1 和干扰素 β 的调节剂。
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5
Delayed induction of proinflammatory cytokines and suppression of innate antiviral response by the novel Middle East respiratory syndrome coronavirus: implications for pathogenesis and treatment.新型中东呼吸综合征冠状病毒致促炎细胞因子延迟产生和固有抗病毒反应受抑制:对发病机制和治疗的影响。
J Gen Virol. 2013 Dec;94(Pt 12):2679-2690. doi: 10.1099/vir.0.055533-0. Epub 2013 Sep 28.
6
Transcriptional regulation by STAT1 and STAT2 in the interferon JAK-STAT pathway.干扰素JAK-STAT途径中STAT1和STAT2的转录调控。
JAKSTAT. 2013 Jul 1;2(3):e23931. doi: 10.4161/jkst.23931. Epub 2013 Jun 18.
7
MicroRNA expression profile of mouse lung infected with 2009 pandemic H1N1 influenza virus.2009 年大流行 H1N1 流感病毒感染小鼠肺组织的 microRNA 表达谱
PLoS One. 2013 Sep 16;8(9):e74190. doi: 10.1371/journal.pone.0074190. eCollection 2013.
8
Curcumin prevents replication of respiratory syncytial virus and the epithelial responses to it in human nasal epithelial cells.姜黄素可预防呼吸道合胞病毒在人鼻腔上皮细胞中的复制及其对其的上皮反应。
PLoS One. 2013 Sep 18;8(9):e70225. doi: 10.1371/journal.pone.0070225. eCollection 2013.
9
The human interferon-induced MxA protein inhibits early stages of influenza A virus infection by retaining the incoming viral genome in the cytoplasm.人干扰素诱导的 MxA 蛋白通过将进入的病毒基因组滞留在细胞质中来抑制甲型流感病毒感染的早期阶段。
J Virol. 2013 Dec;87(23):13053-8. doi: 10.1128/JVI.02220-13. Epub 2013 Sep 18.
10
Treatment with interferon-α2b and ribavirin improves outcome in MERS-CoV-infected rhesus macaques.用干扰素-α2b 和利巴韦林治疗可改善 MERS-CoV 感染恒河猴的预后。
Nat Med. 2013 Oct;19(10):1313-7. doi: 10.1038/nm.3362. Epub 2013 Sep 8.