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The Biology of Persistent Infection: Inflammation and Demyelination following Murine Coronavirus Infection of the Central Nervous System.持续性感染的生物学:小鼠冠状病毒感染中枢神经系统后的炎症与脱髓鞘
Curr Immunol Rev. 2009 May 4;5(4):267-276. doi: 10.2174/157339509789504005.
2
The pathogenesis of murine coronavirus infection of the central nervous system.小鼠冠状病毒感染中枢神经系统的发病机制。
Crit Rev Immunol. 2010;30(2):119-30. doi: 10.1615/critrevimmunol.v30.i2.20.
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J Virol. 2020 Jul 1;94(14). doi: 10.1128/JVI.00548-20.
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Ablation of microglia following infection of the central nervous system with a neurotropic murine coronavirus infection leads to increased demyelination and impaired remyelination.用嗜神经性鼠冠状病毒感染中枢神经系统后,小胶质细胞的消融会导致脱髓鞘增加和髓鞘再生受损。
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Single-Cell RNA Sequencing Reveals the Diversity of the Immunological Landscape following Central Nervous System Infection by a Murine Coronavirus.单细胞RNA测序揭示了小鼠冠状病毒感染中枢神经系统后免疫格局的多样性。
J Virol. 2020 Nov 23;94(24). doi: 10.1128/JVI.01295-20.
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Cystatin F attenuates neuroinflammation and demyelination following murine coronavirus infection of the central nervous system.cystatin F 可减轻鼠冠状病毒感染中枢神经系统后的神经炎症和脱髓鞘。
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Cell replacement therapies to promote remyelination in a viral model of demyelination.细胞替代疗法促进脱髓鞘病毒模型中的髓鞘再生。
J Neuroimmunol. 2010 Jul 27;224(1-2):101-7. doi: 10.1016/j.jneuroim.2010.05.013. Epub 2010 Jun 2.
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Promoting remyelination: utilizing a viral model of demyelination to assess cell-based therapies.促进髓鞘再生:利用脱髓鞘病毒模型评估基于细胞的疗法。
Expert Rev Neurother. 2014 Oct;14(10):1169-79. doi: 10.1586/14737175.2014.955854.
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Disrupted CXCR2 Signaling in Oligodendroglia Lineage Cells Enhances Myelin Repair in a Viral Model of Multiple Sclerosis.少突胶质细胞谱系细胞中 CXCR2 信号的破坏增强了多发性硬化症病毒模型中的髓鞘修复。
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A. Juss Ameliorates Mouse Hepatitis Virus-Induced Neuroinflammatory Demyelination by Modulating Cell-to-Cell Fusion in an Experimental Animal Model of Multiple Sclerosis.A. Juss通过在多发性硬化症实验动物模型中调节细胞间融合改善小鼠肝炎病毒诱导的神经炎性脱髓鞘。
Front Cell Neurosci. 2020 May 12;14:116. doi: 10.3389/fncel.2020.00116. eCollection 2020.

引用本文的文献

1
Cystatin F attenuates neuroinflammation and demyelination following murine coronavirus infection of the central nervous system.cystatin F 可减轻鼠冠状病毒感染中枢神经系统后的神经炎症和脱髓鞘。
J Neuroinflammation. 2024 Jun 15;21(1):157. doi: 10.1186/s12974-024-03153-0.
2
Ablation of microglia following infection of the central nervous system with a neurotropic murine coronavirus infection leads to increased demyelination and impaired remyelination.用嗜神经性鼠冠状病毒感染中枢神经系统后,小胶质细胞的消融会导致脱髓鞘增加和髓鞘再生受损。
J Neuroimmunol. 2023 Aug 15;381:578133. doi: 10.1016/j.jneuroim.2023.578133. Epub 2023 Jun 17.
3
Single-Cell RNA Sequencing Reveals the Diversity of the Immunological Landscape following Central Nervous System Infection by a Murine Coronavirus.单细胞RNA测序揭示了小鼠冠状病毒感染中枢神经系统后免疫格局的多样性。
J Virol. 2020 Nov 23;94(24). doi: 10.1128/JVI.01295-20.
4
Microglia influence host defense, disease, and repair following murine coronavirus infection of the central nervous system.小胶质细胞影响宿主防御、疾病和修复在小鼠冠状病毒感染中枢神经系统后。
Glia. 2020 Nov;68(11):2345-2360. doi: 10.1002/glia.23844. Epub 2020 May 25.
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Regulatory T cells promote remyelination in the murine experimental autoimmune encephalomyelitis model of multiple sclerosis following human neural stem cell transplant.调节性 T 细胞促进多发性硬化症实验性自身免疫性脑脊髓炎模型中人类神经干细胞移植后的髓鞘再生。
Neurobiol Dis. 2020 Jul;140:104868. doi: 10.1016/j.nbd.2020.104868. Epub 2020 Apr 8.
6
Disrupted CXCR2 Signaling in Oligodendroglia Lineage Cells Enhances Myelin Repair in a Viral Model of Multiple Sclerosis.少突胶质细胞谱系细胞中 CXCR2 信号的破坏增强了多发性硬化症病毒模型中的髓鞘修复。
J Virol. 2019 Aug 28;93(18). doi: 10.1128/JVI.00240-19. Print 2019 Sep 15.
7
Innate Immune Responses and Viral-Induced Neurologic Disease.固有免疫反应与病毒诱导的神经疾病
J Clin Med. 2018 Dec 20;8(1):3. doi: 10.3390/jcm8010003.
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Promoting remyelination through cell transplantation therapies in a model of viral-induced neurodegenerative disease.通过细胞移植疗法在病毒诱导的神经退行性疾病模型中促进髓鞘再生。
Dev Dyn. 2019 Jan;248(1):43-52. doi: 10.1002/dvdy.24658. Epub 2018 Sep 6.
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MicroRNA-155 enhances T cell trafficking and antiviral effector function in a model of coronavirus-induced neurologic disease.在冠状病毒诱导的神经疾病模型中,微小RNA-155增强T细胞运输和抗病毒效应功能。
J Neuroinflammation. 2016 Sep 7;13(1):240. doi: 10.1186/s12974-016-0699-z.
10
Sphingosine-1-phosphate receptor antagonism enhances proliferation and migration of engrafted neural progenitor cells in a model of viral-induced demyelination.在病毒诱导的脱髓鞘模型中,鞘氨醇-1-磷酸受体拮抗作用增强了植入的神经祖细胞的增殖和迁移。
Am J Pathol. 2015 Oct;185(10):2819-32. doi: 10.1016/j.ajpath.2015.06.009.

本文引用的文献

1
Age-dependent epigenetic control of differentiation inhibitors is critical for remyelination efficiency.分化抑制剂的年龄依赖性表观遗传控制对髓鞘再生效率至关重要。
Nat Neurosci. 2008 Sep;11(9):1024-34. doi: 10.1038/nn.2172.
2
Neuroprotective effect of transplanted human embryonic stem cell-derived neural precursors in an animal model of multiple sclerosis.人胚胎干细胞源性神经前体细胞移植在多发性硬化动物模型中的神经保护作用
PLoS One. 2008 Sep 5;3(9):e3145. doi: 10.1371/journal.pone.0003145.
3
Repeated subcutaneous injections of IL12/23 p40 neutralising antibody, ustekinumab, in patients with relapsing-remitting multiple sclerosis: a phase II, double-blind, placebo-controlled, randomised, dose-ranging study.复发缓解型多发性硬化症患者皮下重复注射IL12/23 p40中和抗体优特克单抗:一项II期、双盲、安慰剂对照、随机、剂量范围研究。
Lancet Neurol. 2008 Sep;7(9):796-804. doi: 10.1016/S1474-4422(08)70173-X.
4
An experimental model of secondary progressive multiple sclerosis that shows regional variation in gliosis, remyelination, axonal and neuronal loss.一种继发性进展型多发性硬化症的实验模型,该模型显示了胶质增生、髓鞘再生、轴突和神经元损失的区域差异。
J Neuroimmunol. 2008 Sep 15;201-202:200-11. doi: 10.1016/j.jneuroim.2008.05.034. Epub 2008 Jul 30.
5
Temporal trends in the incidence of multiple sclerosis: a systematic review.多发性硬化症发病率的时间趋势:一项系统综述。
Neurology. 2008 Jul 8;71(2):129-35. doi: 10.1212/01.wnl.0000316802.35974.34.
6
Generation of a protective T-cell response following coronavirus infection of the central nervous system is not dependent on IL-12/23 signaling.冠状病毒感染中枢神经系统后产生保护性T细胞反应并不依赖于IL-12/23信号传导。
Viral Immunol. 2008 Jun;21(2):173-88. doi: 10.1089/vim.2008.0014.
7
Varicella-zoster virus in cerebrospinal fluid at relapses of multiple sclerosis.多发性硬化复发时脑脊液中的水痘带状疱疹病毒
Ann Neurol. 2008 Mar;63(3):303-11. doi: 10.1002/ana.21316.
8
CXCR3 mediates region-specific antiviral T cell trafficking within the central nervous system during West Nile virus encephalitis.在西尼罗河病毒脑炎期间,CXCR3介导中枢神经系统内区域特异性抗病毒T细胞的迁移。
J Immunol. 2008 Feb 15;180(4):2641-9. doi: 10.4049/jimmunol.180.4.2641.
9
CXCL9 and CXCL10 expression are critical for control of genital herpes simplex virus type 2 infection through mobilization of HSV-specific CTL and NK cells to the nervous system.CXCL9和CXCL10的表达对于通过将单纯疱疹病毒2型特异性CTL和NK细胞动员至神经系统来控制生殖器单纯疱疹病毒2型感染至关重要。
J Immunol. 2008 Jan 15;180(2):1098-106. doi: 10.4049/jimmunol.180.2.1098.
10
NKG2D receptor signaling enhances cytolytic activity by virus-specific CD8+ T cells: evidence for a protective role in virus-induced encephalitis.NKG2D受体信号传导增强病毒特异性CD8 + T细胞的细胞溶解活性:在病毒诱导的脑炎中起保护作用的证据。
J Virol. 2008 Mar;82(6):3031-44. doi: 10.1128/JVI.02033-07. Epub 2007 Dec 26.

持续性感染的生物学:小鼠冠状病毒感染中枢神经系统后的炎症与脱髓鞘

The Biology of Persistent Infection: Inflammation and Demyelination following Murine Coronavirus Infection of the Central Nervous System.

作者信息

Hosking Martin P, Lane Thomas E

机构信息

Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697-3900 USA.

出版信息

Curr Immunol Rev. 2009 May 4;5(4):267-276. doi: 10.2174/157339509789504005.

DOI:10.2174/157339509789504005
PMID:19946572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2782875/
Abstract

Multiple Sclerosis (MS) is an immune-mediated demyelinating disease of humans. Although causes of MS are enigmatic, underlying elements contributing to disease development include both genetic and environmental factors. Recent epidemiological evidence has pointed to viral infection as a trigger to initiating white matter damage in humans. Mouse hepatitis virus (MHV) is a positive strand RNA virus that, following intracranial infection of susceptible mice, induces an acute encephalomyelitis that later resolves into a chronic fulminating demyelinating disease. Immune cell infiltration into the central nervous system is critical both to quell viral replication and instigate demyelination. Recent efforts by our laboratory and others have focused upon strategies capable of enhancing remyelination in response to viral-induced demyelination, both by dampening chronic inflammation and by surgical engraftment of remyelination - competent neural precursor cells.

摘要

多发性硬化症(MS)是一种人类免疫介导的脱髓鞘疾病。尽管MS的病因尚不明确,但导致疾病发展的潜在因素包括遗传和环境因素。最近的流行病学证据表明,病毒感染是引发人类白质损伤的诱因。小鼠肝炎病毒(MHV)是一种正链RNA病毒,在易感小鼠颅内感染后,会诱发急性脑脊髓炎,随后发展为慢性暴发性脱髓鞘疾病。免疫细胞浸润到中枢神经系统对于抑制病毒复制和引发脱髓鞘至关重要。我们实验室和其他研究团队最近的工作重点是通过抑制慢性炎症和手术植入具有髓鞘再生能力的神经前体细胞,来增强对病毒诱导的脱髓鞘的髓鞘再生反应。