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Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis.


ABSTRACT: 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.

SUBMITTER: Leibovitch EC 

PROVIDER: S-EPMC6217390 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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Herpesvirus trigger accelerates neuroinflammation in a nonhuman primate model of multiple sclerosis.

Leibovitch Emily C EC   Caruso Breanna B   Caruso Breanna B   Ha Seung Kwon SK   Schindler Matthew K MK   Lee Nathanael J NJ   Luciano Nicholas J NJ   Billioux Bridgette J BJ   Guy Joseph R JR   Yen Cecil C   Sati Pascal P   Silva Afonso C AC   Reich Daniel S DS   Jacobson Steven S  

Proceedings of the National Academy of Sciences of the United States of America 20181015 44


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). Altho  ...[more]

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