• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Measure and countermeasure: type I IFN (IFN-alpha/beta) antiviral response against West Nile virus.措施与对策:I 型干扰素(IFN-α/β)对西尼罗河病毒的抗病毒反应。
J Innate Immun. 2009;1(5):435-45. doi: 10.1159/000226248. Epub 2009 Jun 24.
2
Alpha/beta interferon protects against lethal West Nile virus infection by restricting cellular tropism and enhancing neuronal survival.α/β干扰素通过限制细胞嗜性和增强神经元存活来预防西尼罗河病毒致死性感染。
J Virol. 2005 Nov;79(21):13350-61. doi: 10.1128/JVI.79.21.13350-13361.2005.
3
Resistance to alpha/beta interferon is a determinant of West Nile virus replication fitness and virulence.对α/β干扰素的抗性是西尼罗河病毒复制适应性和毒力的一个决定因素。
J Virol. 2006 Oct;80(19):9424-34. doi: 10.1128/JVI.00768-06.
4
A systems biology approach reveals that tissue tropism to West Nile virus is regulated by antiviral genes and innate immune cellular processes.系统生物学方法揭示,组织对西尼罗河病毒的嗜性受抗病毒基因和固有免疫细胞过程的调节。
PLoS Pathog. 2013 Feb;9(2):e1003168. doi: 10.1371/journal.ppat.1003168. Epub 2013 Feb 7.
5
A single amino acid substitution in the West Nile virus nonstructural protein NS2A disables its ability to inhibit alpha/beta interferon induction and attenuates virus virulence in mice.西尼罗河病毒非结构蛋白NS2A中的单个氨基酸替换使其丧失抑制α/β干扰素诱导的能力,并减弱了病毒在小鼠中的毒力。
J Virol. 2006 Mar;80(5):2396-404. doi: 10.1128/JVI.80.5.2396-2404.2006.
6
West Nile Virus-Inclusive Single-Cell RNA Sequencing Reveals Heterogeneity in the Type I Interferon Response within Single Cells.西尼罗河病毒全基因组单细胞 RNA 测序揭示了单个细胞中 I 型干扰素反应的异质性。
J Virol. 2019 Mar 5;93(6). doi: 10.1128/JVI.01778-18. Print 2019 Mar 15.
7
VAMP8 Contributes to the TRIM6-Mediated Type I Interferon Antiviral Response during West Nile Virus Infection.VAMP8 有助于西尼罗河病毒感染过程中 TRIM6 介导的 I 型干扰素抗病毒反应。
J Virol. 2020 Jan 6;94(2). doi: 10.1128/JVI.01454-19.
8
Gamma interferon plays a crucial early antiviral role in protection against West Nile virus infection.γ干扰素在抵御西尼罗河病毒感染的早期抗病毒过程中发挥着关键作用。
J Virol. 2006 Jun;80(11):5338-48. doi: 10.1128/JVI.00274-06.
9
Cell-specific IRF-3 responses protect against West Nile virus infection by interferon-dependent and -independent mechanisms.细胞特异性IRF-3反应通过干扰素依赖和非依赖机制抵御西尼罗河病毒感染。
PLoS Pathog. 2007 Jul 27;3(7):e106. doi: 10.1371/journal.ppat.0030106.
10
Interferon regulatory factor IRF-7 induces the antiviral alpha interferon response and protects against lethal West Nile virus infection.干扰素调节因子IRF-7诱导抗病毒α干扰素反应并抵御西尼罗河病毒致死性感染。
J Virol. 2008 Sep;82(17):8465-75. doi: 10.1128/JVI.00918-08. Epub 2008 Jun 18.

引用本文的文献

1
Encephalomyocarditis virus protein 2B* interacts with 14-3-3 proteins through a phosphorylated C-terminal binding motif.脑心肌炎病毒蛋白2B*通过磷酸化的C末端结合基序与14-3-3蛋白相互作用。
mBio. 2025 Aug 18:e0100825. doi: 10.1128/mbio.01008-25.
2
CD11b maintains West Nile virus replication through modulation of immune response in human neuroblastoma cells.CD11b 通过调节人神经母细胞瘤细胞的免疫反应来维持西尼罗河病毒的复制。
Virol J. 2024 Jul 14;21(1):158. doi: 10.1186/s12985-024-02427-6.
3
Engagement of AKT and ERK signaling pathways facilitates infection of human neuronal cells with West Nile virus.AKT和ERK信号通路的激活促进西尼罗河病毒对人神经元细胞的感染。
J Virus Erad. 2024 Mar 28;10(1):100368. doi: 10.1016/j.jve.2024.100368. eCollection 2024 Mar.
4
Blockade of interferon signaling decreases gut barrier integrity and promotes severe West Nile virus disease.阻断干扰素信号通路会降低肠道屏障的完整性,并促进西尼罗河病毒病的严重化。
Nat Commun. 2023 Sep 25;14(1):5973. doi: 10.1038/s41467-023-41600-3.
5
Flaviviruses: Innate Immunity, Inflammasome Activation, Inflammatory Cell Death, and Cytokines.黄病毒:先天免疫、炎症小体激活、炎症细胞死亡和细胞因子。
Front Immunol. 2022 Jan 28;13:829433. doi: 10.3389/fimmu.2022.829433. eCollection 2022.
6
Host Factors That Control Mosquito-Borne Viral Infections in Humans and Their Vector.控制人类与蚊媒病毒感染及其媒介的宿主因素。
Viruses. 2021 Apr 24;13(5):748. doi: 10.3390/v13050748.
7
Pathogenicity and virulence of West Nile virus revisited eight decades after its first isolation.时隔西尼罗河病毒首次分离 80 年后再探其致病性和毒力。
Virulence. 2021 Dec;12(1):1145-1173. doi: 10.1080/21505594.2021.1908740.
8
Alpha/Beta Interferon (IFN-α/β) Signaling in Astrocytes Mediates Protection against Viral Encephalomyelitis and Regulates IFN-γ-Dependent Responses.星形胶质细胞中的 Alpha/Beta 干扰素 (IFN-α/β) 信号转导介导对病毒性脑脊髓炎的保护作用,并调节 IFN-γ 依赖性反应。
J Virol. 2018 Apr 27;92(10). doi: 10.1128/JVI.01901-17. Print 2018 May 15.
9
Splenic macrophages are required for protective innate immunity against West Nile virus.脾脏巨噬细胞是抵抗西尼罗河病毒的保护性固有免疫所必需的。
PLoS One. 2018 Feb 6;13(2):e0191690. doi: 10.1371/journal.pone.0191690. eCollection 2018.
10
Zika Virus Exhibits Lineage-Specific Phenotypes in Cell Culture, in Aedes aegypti Mosquitoes, and in an Embryo Model.寨卡病毒在细胞培养、埃及伊蚊和胚胎模型中表现出谱系特异性表型。
Viruses. 2017 Dec 16;9(12):383. doi: 10.3390/v9120383.

本文引用的文献

1
Toll-like receptor 7 mitigates lethal West Nile encephalitis via interleukin 23-dependent immune cell infiltration and homing.Toll样受体7通过白细胞介素23依赖的免疫细胞浸润和归巢减轻致死性西尼罗河脑炎。
Immunity. 2009 Feb 20;30(2):242-53. doi: 10.1016/j.immuni.2008.11.012. Epub 2009 Feb 5.
2
TLR4 ligands induce IFN-alpha production by mouse conventional dendritic cells and human monocytes after IFN-beta priming.在经干扰素-β 预刺激后,Toll样受体4(TLR4)配体可诱导小鼠传统树突状细胞和人单核细胞产生干扰素-α。
J Immunol. 2009 Jan 15;182(2):820-8. doi: 10.4049/jimmunol.182.2.820.
3
RNA recognition and signal transduction by RIG-I-like receptors.维甲酸诱导基因I样受体介导的RNA识别与信号转导
Immunol Rev. 2009 Jan;227(1):54-65. doi: 10.1111/j.1600-065X.2008.00727.x.
4
Cytosolic viral sensor RIG-I is a 5'-triphosphate-dependent translocase on double-stranded RNA.胞质病毒传感器视黄酸诱导基因I(RIG-I)是一种依赖于5'-三磷酸的双链RNA转位酶。
Science. 2009 Feb 20;323(5917):1070-4. doi: 10.1126/science.1168352. Epub 2009 Jan 1.
5
Toll-like receptor 3 has a protective role against West Nile virus infection.Toll样受体3对西尼罗河病毒感染具有保护作用。
J Virol. 2008 Nov;82(21):10349-58. doi: 10.1128/JVI.00935-08. Epub 2008 Aug 20.
6
Pathogen recognition by innate receptors.天然受体对病原体的识别。
J Infect Chemother. 2008 Apr;14(2):86-92. doi: 10.1007/s10156-008-0596-1. Epub 2008 Apr 30.
7
Differential recognition of double-stranded RNA by RIG-I-like receptors in antiviral immunity.抗病毒免疫中RIG-I样受体对双链RNA的差异性识别
J Exp Med. 2008 Jul 7;205(7):1523-7. doi: 10.1084/jem.20081210.
8
Length-dependent recognition of double-stranded ribonucleic acids by retinoic acid-inducible gene-I and melanoma differentiation-associated gene 5.视黄酸诱导基因-I和黑色素瘤分化相关基因5对双链核糖核酸的长度依赖性识别
J Exp Med. 2008 Jul 7;205(7):1601-10. doi: 10.1084/jem.20080091.
9
Interferon regulatory factor IRF-7 induces the antiviral alpha interferon response and protects against lethal West Nile virus infection.干扰素调节因子IRF-7诱导抗病毒α干扰素反应并抵御西尼罗河病毒致死性感染。
J Virol. 2008 Sep;82(17):8465-75. doi: 10.1128/JVI.00918-08. Epub 2008 Jun 18.
10
West Nile virus nonstructural protein 1 inhibits TLR3 signal transduction.西尼罗河病毒非结构蛋白1抑制Toll样受体3信号转导。
J Virol. 2008 Sep;82(17):8262-71. doi: 10.1128/JVI.00226-08. Epub 2008 Jun 18.

措施与对策:I 型干扰素(IFN-α/β)对西尼罗河病毒的抗病毒反应。

Measure and countermeasure: type I IFN (IFN-alpha/beta) antiviral response against West Nile virus.

机构信息

Department of Medicine, Washington University School of Medicine, St Louis, MO 63110, USA.

出版信息

J Innate Immun. 2009;1(5):435-45. doi: 10.1159/000226248. Epub 2009 Jun 24.

DOI:10.1159/000226248
PMID:20375601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2920482/
Abstract

As a first line of defense after viral infection, host cells develop an intrinsic immune response to control virus dissemination and protect against serious infection. Recent experiments have shown a dominant role of the IFN-alpha/beta response in protection against lethal West Nile virus (WNV) by limiting the cellular and tissue tropism of infection. This review will focus on advances in identifying the host sensors that detect WNV and the adaptor molecules and signaling pathways that regulate the induction of IFN-alpha/beta defenses that limit WNV replication, spread and pathogenesis.

摘要

作为病毒感染后的第一道防线,宿主细胞会产生固有免疫反应来控制病毒传播并防止严重感染。最近的实验表明,IFN-α/β反应在限制西尼罗河病毒(WNV)的细胞和组织嗜性方面发挥了主导作用,从而对保护机体免受致命性WNV 感染具有重要作用。本综述将重点介绍鉴定宿主传感器以识别 WNV 的研究进展,以及调节 IFN-α/β防御反应诱导的衔接分子和信号通路,这些反应可以限制 WNV 的复制、传播和发病机制。