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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
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.
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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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