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Decreased antiviral immune response within the central nervous system of aged mice is associated with increased lethality of West Nile virus encephalitis.
Funk, Kristen E; Arutyunov, Artem D; Desai, Pritesh; White, James P; Soung, Allison L; Rosen, Sarah F; Diamond, Michael S; Klein, Robyn S.
Afiliación
  • Funk KE; Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Arutyunov AD; Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Desai P; Center for Neuroimmunology and Neuroinfectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • White JP; Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Soung AL; Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Rosen SF; Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Diamond MS; Center for Neuroimmunology and Neuroinfectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Klein RS; Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, USA.
Aging Cell ; 20(8): e13412, 2021 08.
Article en En | MEDLINE | ID: mdl-34327802
West Nile virus (WNV) is an emerging pathogen that causes disease syndromes ranging from a mild flu-like illness to encephalitis. While the incidence of WNV infection is fairly uniform across age groups, the risk of lethal encephalitis increases with advanced age. Prior studies have demonstrated age-related, functional immune deficits that limit systemic antiviral immunity and increase mortality; however, the effect of age on antiviral immune responses specifically within the central nervous system (CNS) is unknown. Here, we show that aged mice exhibit increased peripheral organ and CNS tissue viral burden, the latter of which is associated with alterations in activation of both myeloid and lymphoid cells compared with similarly infected younger animals. Aged mice exhibit lower MHCII expression by microglia, and higher levels of PD1 and lower levels of IFNγ expression by WNV-specific CD8+ T cells in the CNS and CD8+ CD45+ cells. These data indicate that the aged CNS exhibits limited local reactivation of T cells during viral encephalitis, which may lead to reduced virologic control at this site.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fiebre del Nilo Occidental / Sistema Nervioso Central / Inmunidad Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Aging Cell Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fiebre del Nilo Occidental / Sistema Nervioso Central / Inmunidad Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Aging Cell Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido