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Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis
Multiple sclerosis (MS) is a neuroinflammatory and neurodegenerative disease of unknown etiology. However, several studies suggest that infectious agents, e.g., Human Herpes Viruses (HHV), may be involved in triggering the disease. Molecular mimicry, bystander effect, and epitope spreading are three...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606571/ https://www.ncbi.nlm.nih.gov/pubmed/36311024 http://dx.doi.org/10.3389/fnmol.2022.1019799 |
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author | Pike, Steven C. Welsh, Nora Linzey, Michael Gilli, Francesca |
author_facet | Pike, Steven C. Welsh, Nora Linzey, Michael Gilli, Francesca |
author_sort | Pike, Steven C. |
collection | PubMed |
description | Multiple sclerosis (MS) is a neuroinflammatory and neurodegenerative disease of unknown etiology. However, several studies suggest that infectious agents, e.g., Human Herpes Viruses (HHV), may be involved in triggering the disease. Molecular mimicry, bystander effect, and epitope spreading are three mechanisms that can initiate immunoreactivity leading to CNS autoimmunity in MS. Theiler’s murine encephalomyelitis virus (TMEV)-induced demyelinating disease (TMEV-IDD) is a pre-clinical model of MS in which intracerebral inoculation of TMEV results in a CNS autoimmune disease that causes demyelination, neuroaxonal damage, and progressive clinical disability. Given the spectra of different murine models used to study MS, this review highlights why TMEV-IDD represents a valuable tool for testing the viral hypotheses of MS. We initially describe how the main mechanisms of CNS autoimmunity have been identified across both MS and TMEV-IDD etiology. Next, we discuss how adaptive, innate, and CNS resident immune cells contribute to TMEV-IDD immunopathology and how this relates to MS. Lastly, we highlight the sexual dimorphism observed in TMEV-IDD and MS and how this may be tied to sexually dimorphic responses to viral infections. In summary, TMEV-IDD is an underutilized murine model that recapitulates many unique aspects of MS; as we learn more about the nature of viral infections in MS, TMEV-IDD will be critical in testing the future therapeutics that aim to intervene with disease onset and progression. |
format | Online Article Text |
id | pubmed-9606571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96065712022-10-28 Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis Pike, Steven C. Welsh, Nora Linzey, Michael Gilli, Francesca Front Mol Neurosci Neuroscience Multiple sclerosis (MS) is a neuroinflammatory and neurodegenerative disease of unknown etiology. However, several studies suggest that infectious agents, e.g., Human Herpes Viruses (HHV), may be involved in triggering the disease. Molecular mimicry, bystander effect, and epitope spreading are three mechanisms that can initiate immunoreactivity leading to CNS autoimmunity in MS. Theiler’s murine encephalomyelitis virus (TMEV)-induced demyelinating disease (TMEV-IDD) is a pre-clinical model of MS in which intracerebral inoculation of TMEV results in a CNS autoimmune disease that causes demyelination, neuroaxonal damage, and progressive clinical disability. Given the spectra of different murine models used to study MS, this review highlights why TMEV-IDD represents a valuable tool for testing the viral hypotheses of MS. We initially describe how the main mechanisms of CNS autoimmunity have been identified across both MS and TMEV-IDD etiology. Next, we discuss how adaptive, innate, and CNS resident immune cells contribute to TMEV-IDD immunopathology and how this relates to MS. Lastly, we highlight the sexual dimorphism observed in TMEV-IDD and MS and how this may be tied to sexually dimorphic responses to viral infections. In summary, TMEV-IDD is an underutilized murine model that recapitulates many unique aspects of MS; as we learn more about the nature of viral infections in MS, TMEV-IDD will be critical in testing the future therapeutics that aim to intervene with disease onset and progression. Frontiers Media S.A. 2022-10-13 /pmc/articles/PMC9606571/ /pubmed/36311024 http://dx.doi.org/10.3389/fnmol.2022.1019799 Text en Copyright © 2022 Pike, Welsh, Linzey and Gilli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Pike, Steven C. Welsh, Nora Linzey, Michael Gilli, Francesca Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
title | Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
title_full | Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
title_fullStr | Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
title_full_unstemmed | Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
title_short | Theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
title_sort | theiler’s virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606571/ https://www.ncbi.nlm.nih.gov/pubmed/36311024 http://dx.doi.org/10.3389/fnmol.2022.1019799 |
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