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Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis
Pathogens, particularly human herpesviruses (HHVs), are implicated as triggers of disease onset/progression in multiple sclerosis (MS) and other neuroinflammatory disorders. However, the time between viral acquisition in childhood and disease onset in adulthood complicates the study of this associat...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217390/ https://www.ncbi.nlm.nih.gov/pubmed/30322946 http://dx.doi.org/10.1073/pnas.1811974115 |
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author | Leibovitch, Emily C. Caruso, Breanna Ha, Seung Kwon Schindler, Matthew K. Lee, Nathanael J. Luciano, Nicholas J. Billioux, Bridgette J. Guy, Joseph R. Yen, Cecil Sati, Pascal Silva, Afonso C. Reich, Daniel S. Jacobson, Steven |
author_facet | Leibovitch, Emily C. Caruso, Breanna Ha, Seung Kwon Schindler, Matthew K. Lee, Nathanael J. Luciano, Nicholas J. Billioux, Bridgette J. Guy, Joseph R. Yen, Cecil Sati, Pascal Silva, Afonso C. Reich, Daniel S. Jacobson, Steven |
author_sort | Leibovitch, Emily C. |
collection | PubMed |
description | Pathogens, particularly human herpesviruses (HHVs), are implicated as triggers of disease onset/progression in multiple sclerosis (MS) and other neuroinflammatory disorders. However, the time between viral acquisition in childhood and disease onset in adulthood complicates the study of this association. Using nonhuman primates, we demonstrate that intranasal inoculations with HHV-6A and HHV-6B accelerate an MS-like neuroinflammatory disease, experimental autoimmune encephalomyelitis (EAE). Although animals inoculated intranasally with HHV-6 (virus/EAE marmosets) were asymptomatic, they exhibited significantly accelerated clinical EAE compared with control animals. Expansion of a proinflammatory CD8 subset correlated with post-EAE survival in virus/EAE marmosets, suggesting that a peripheral (viral?) antigen-driven expansion may have occurred post-EAE induction. HHV-6 viral antigen in virus/EAE marmosets was markedly elevated and concentrated in brain lesions, similar to previously reported localizations of HHV-6 in MS brain lesions. Collectively, we demonstrate that asymptomatic intranasal viral acquisition accelerates subsequent neuroinflammation in a nonhuman primate model of MS. |
format | Online Article Text |
id | pubmed-6217390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-62173902018-11-06 Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis Leibovitch, Emily C. Caruso, Breanna Ha, Seung Kwon Schindler, Matthew K. Lee, Nathanael J. Luciano, Nicholas J. Billioux, Bridgette J. Guy, Joseph R. Yen, Cecil Sati, Pascal Silva, Afonso C. Reich, Daniel S. Jacobson, Steven Proc Natl Acad Sci U S A Biological Sciences Pathogens, particularly human herpesviruses (HHVs), are implicated as triggers of disease onset/progression in multiple sclerosis (MS) and other neuroinflammatory disorders. However, the time between viral acquisition in childhood and disease onset in adulthood complicates the study of this association. Using nonhuman primates, we demonstrate that intranasal inoculations with HHV-6A and HHV-6B accelerate an MS-like neuroinflammatory disease, experimental autoimmune encephalomyelitis (EAE). Although animals inoculated intranasally with HHV-6 (virus/EAE marmosets) were asymptomatic, they exhibited significantly accelerated clinical EAE compared with control animals. Expansion of a proinflammatory CD8 subset correlated with post-EAE survival in virus/EAE marmosets, suggesting that a peripheral (viral?) antigen-driven expansion may have occurred post-EAE induction. HHV-6 viral antigen in virus/EAE marmosets was markedly elevated and concentrated in brain lesions, similar to previously reported localizations of HHV-6 in MS brain lesions. Collectively, we demonstrate that asymptomatic intranasal viral acquisition accelerates subsequent neuroinflammation in a nonhuman primate model of MS. National Academy of Sciences 2018-10-30 2018-10-15 /pmc/articles/PMC6217390/ /pubmed/30322946 http://dx.doi.org/10.1073/pnas.1811974115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Leibovitch, Emily C. Caruso, Breanna Ha, Seung Kwon Schindler, Matthew K. Lee, Nathanael J. Luciano, Nicholas J. Billioux, Bridgette J. Guy, Joseph R. Yen, Cecil Sati, Pascal Silva, Afonso C. Reich, Daniel S. Jacobson, Steven Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
title | Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
title_full | Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
title_fullStr | Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
title_full_unstemmed | Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
title_short | Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
title_sort | herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217390/ https://www.ncbi.nlm.nih.gov/pubmed/30322946 http://dx.doi.org/10.1073/pnas.1811974115 |
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