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90 岁高龄仍患实验性脑脊髓炎,该病例仍然具有相关性,并阐明了病毒如何引发疾病。

Experimental encephalomyelitis at age 90, still relevant and elucidating how viruses trigger disease.

机构信息

Department of Neurology and Neurological Sciences and Pediatrics, Stanford University , Stanford, CA, USA.

Access Health International , Ridgefield, CT, USA.

出版信息

J Exp Med. 2023 Feb 6;220(2). doi: 10.1084/jem.20221322. Epub 2023 Jan 18.


DOI:10.1084/jem.20221322
PMID:36652203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9880878/
Abstract

20 yr ago, a tribute appeared in this journal on the 70th anniversary of an animal model of disseminated encephalomyelitis, abbreviated EAE for experimental autoimmune encephalomyelitis. "Observations on Attempts to Produce Disseminated Encephalomyelitis in Monkeys" appeared in the Journal of Experimental Medicine on February 21, 1933. Rivers and colleagues were trying to understand what caused neurological reactions to viral infections like smallpox, vaccinia, and measles, and what triggered rare instances of encephalomyelitis to smallpox vaccines. The animal model known as EAE continues to display its remarkable utility. Recent research, since the 70th-anniversary tribute, helps explain how Epstein-Barr virus triggers multiple sclerosis via molecular mimicry to a protein known as GlialCAM. Proteins with multiple domains similar to GlialCAM, tenascin, neuregulin, contactin, and protease kinase C inhibitors are present in the poxvirus family. These observations take us a full circle back to Rivers' first paper on EAE, 90 yr ago.

摘要

20 年前,在这本期刊上发表了一篇纪念文章,纪念实验性自身免疫性脑脊髓炎(EAE)动物模型诞生 70 周年。这篇题为“观察在猴子中诱发弥散性脑脊髓炎的尝试”的文章于 1933 年 2 月 21 日发表在《实验医学杂志》上。里弗斯及其同事试图了解导致天花、牛痘和麻疹等病毒感染引起神经反应的原因,以及导致极少数天花疫苗引发脑脊髓炎的原因。这种被称为 EAE 的动物模型至今仍显示出其显著的效用。自 70 周年纪念文章发表以来的最新研究有助于解释 Epstein-Barr 病毒如何通过分子模拟触发多发性硬化症,从而针对一种名为 GlialCAM 的蛋白。痘病毒家族中存在与 GlialCAM 具有多个相似结构域的蛋白,如 tenascin、neuregulin、contactin 和蛋白酶激酶 C 抑制剂。这些观察结果使我们回到了 90 年前里弗斯关于 EAE 的第一篇论文。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/f83a806505d8/JEM_20221322_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/ddfcc6169176/JEM_20221322_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/542e8a9a1605/JEM_20221322_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/f83a806505d8/JEM_20221322_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/ddfcc6169176/JEM_20221322_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/542e8a9a1605/JEM_20221322_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c23/9880878/f83a806505d8/JEM_20221322_Fig3.jpg

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[8]
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本文引用的文献

[1]
Two Cases of Monkeypox-Associated Encephalomyelitis - Colorado and the District of Columbia, July-August 2022.

MMWR Morb Mortal Wkly Rep. 2022-9-23

[2]
The Extracellular Matrix Proteins Tenascin-C and Tenascin-R Retard Oligodendrocyte Precursor Maturation and Myelin Regeneration in a Cuprizone-Induced Long-Term Demyelination Animal Model.

Cells. 2022-5-28

[3]
Viral Proteins with PxxP and PY Motifs May Play a Role in Multiple Sclerosis.

Viruses. 2022-1-28

[4]
Clonally expanded B cells in multiple sclerosis bind EBV EBNA1 and GlialCAM.

Nature. 2022-3

[5]
Epstein-Barr virus and multiple sclerosis.

Science. 2022-1-21

[6]
Longitudinal analysis reveals high prevalence of Epstein-Barr virus associated with multiple sclerosis.

Science. 2022-1-21

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Structure and function of the poxvirus transcription machinery.

Enzymes. 2021

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The Disease Ecology, Epidemiology, Clinical Manifestations, Management, Prevention, and Control of Increasing Human Infections with Animal Orthopoxviruses.

Wilderness Environ Med. 2021-12

[9]
MiR-142-3p regulates synaptopathy-driven disease progression in multiple sclerosis.

Neuropathol Appl Neurobiol. 2022-2

[10]
Serum contactin-1 as a biomarker of long-term disease progression in natalizumab-treated multiple sclerosis.

Mult Scler. 2022-1

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