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肠道病毒 A71 的固有免疫应答及病毒逃逸策略的最新研究进展。

Recent Progress in Innate Immune Responses to Enterovirus A71 and Viral Evasion Strategies.

机构信息

School of Medicine, Chongqing University, Chongqing 400044, China.

Institute of Precision Medicine, Chongqing University, Chongqing 400044, China.

出版信息

Int J Mol Sci. 2024 May 23;25(11):5688. doi: 10.3390/ijms25115688.

DOI:10.3390/ijms25115688
PMID:38891876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11172324/
Abstract

Enterovirus A71 (EV-A71) is a major pathogen causing hand, foot, and mouth disease (HFMD) in children worldwide. It can lead to severe gastrointestinal, pulmonary, and neurological complications. The innate immune system, which rapidly detects pathogens via pathogen-associated molecular patterns or pathogen-encoded effectors, serves as the first defensive line against EV-A71 infection. Concurrently, the virus has developed various sophisticated strategies to evade host antiviral responses and establish productive infection. Thus, the virus-host interactions and conflicts, as well as the ability to govern biological events at this first line of defense, contribute significantly to the pathogenesis and outcomes of EV-A71 infection. In this review, we update recent progress on host innate immune responses to EV-A71 infection. In addition, we discuss the underlying strategies employed by EV-A71 to escape host innate immune responses. A better understanding of the interplay between EV-A71 and host innate immunity may unravel potential antiviral targets, as well as strategies that can improve patient outcomes.

摘要

肠道病毒 A71(EV-A71)是一种主要病原体,可导致全球儿童手足口病(HFMD)。它可导致严重的胃肠道、肺部和神经系统并发症。先天免疫系统通过病原体相关分子模式或病原体编码的效应子快速检测病原体,是抵御 EV-A71 感染的第一道防线。同时,病毒已经发展出各种复杂的策略来逃避宿主抗病毒反应并建立有效的感染。因此,病毒-宿主相互作用和冲突,以及在这第一道防线中控制生物事件的能力,对 EV-A71 感染的发病机制和结果有重要影响。在这篇综述中,我们更新了宿主对 EV-A71 感染的先天免疫反应的最新进展。此外,我们还讨论了 EV-A71 逃避宿主先天免疫反应的潜在策略。更好地了解 EV-A71 与宿主先天免疫之间的相互作用可能会揭示潜在的抗病毒靶点,以及改善患者预后的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/f00101b2417d/ijms-25-05688-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/b83316745965/ijms-25-05688-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/936924433e28/ijms-25-05688-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/f00101b2417d/ijms-25-05688-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/b83316745965/ijms-25-05688-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/936924433e28/ijms-25-05688-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5362/11172324/f00101b2417d/ijms-25-05688-g003.jpg

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ILC3 Function as a Double-Edged Sword in EV71 Infection.

本文引用的文献

1
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J Virol. 2023 Nov 30;97(11):e0107523. doi: 10.1128/jvi.01075-23. Epub 2023 Oct 17.
2
Secreted LRPAP1 binds and triggers IFNAR1 degradation to facilitate virus evasion from cellular innate immunity.分泌型 LRPAP1 结合并触发 IFNAR1 降解,以促进病毒逃避细胞固有免疫。
Signal Transduct Target Ther. 2023 Sep 25;8(1):374. doi: 10.1038/s41392-023-01630-1.
3
Tripping the wire: sensing of viral protease activity by CARD8 and NLRP1 inflammasomes.
在肠道病毒71型(EV71)感染中,3型固有淋巴细胞(ILC3)起着双刃剑的作用。
Viruses. 2025 Jan 27;17(2):184. doi: 10.3390/v17020184.
4
The N6-methyladenosine RNA epigenetic modification modulates the amplification of coxsackievirus B1 in human pancreatic beta cells.N6-甲基腺苷RNA表观遗传修饰调节柯萨奇病毒B1在人胰岛β细胞中的扩增。
Front Microbiol. 2024 Dec 18;15:1501061. doi: 10.3389/fmicb.2024.1501061. eCollection 2024.
触发机制:CARD8 和 NLRP1 炎性小体对病毒蛋白酶活性的感应。
Curr Opin Immunol. 2023 Aug;83:102354. doi: 10.1016/j.coi.2023.102354. Epub 2023 Jun 11.
4
Host-specific sensing of coronaviruses and picornaviruses by the CARD8 inflammasome.CARD8 炎性小体对冠状病毒和小核糖核酸病毒的宿主特异性感应。
PLoS Biol. 2023 Jun 8;21(6):e3002144. doi: 10.1371/journal.pbio.3002144. eCollection 2023 Jun.
5
The NLR gene family: from discovery to present day.NLR 基因家族:从发现到现在。
Nat Rev Immunol. 2023 Oct;23(10):635-654. doi: 10.1038/s41577-023-00849-x. Epub 2023 Mar 27.
6
Current status of hand-foot-and-mouth disease.手足口病现状。
J Biomed Sci. 2023 Feb 24;30(1):15. doi: 10.1186/s12929-023-00908-4.
7
TRAF3 activates STING-mediated suppression of EV-A71 and target of viral evasion.TRAF3 激活 STING 介导的 EV-A71 抑制和病毒逃避的靶点。
Signal Transduct Target Ther. 2023 Feb 24;8(1):79. doi: 10.1038/s41392-022-01287-2.
8
Effector-Triggered Immunity.效应子触发的免疫
Annu Rev Immunol. 2023 Apr 26;41:453-481. doi: 10.1146/annurev-immunol-101721-031732. Epub 2023 Feb 7.
9
Effector-triggered immunity in mammalian antiviral defense.哺乳动物抗病毒防御中的效应子触发免疫。
Trends Immunol. 2022 Dec;43(12):1006-1017. doi: 10.1016/j.it.2022.10.004. Epub 2022 Nov 8.
10
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Virol Sin. 2023 Feb;38(1):75-83. doi: 10.1016/j.virs.2022.11.001. Epub 2022 Nov 2.