Your browser doesn't support javascript.
loading
A Mouse Model of Chronic West Nile Virus Disease.
Graham, Jessica B; Swarts, Jessica L; Wilkins, Courtney; Thomas, Sunil; Green, Richard; Sekine, Aimee; Voss, Kathleen M; Ireton, Renee C; Mooney, Michael; Choonoo, Gabrielle; Miller, Darla R; Treuting, Piper M; Pardo Manuel de Villena, Fernando; Ferris, Martin T; McWeeney, Shannon; Gale, Michael; Lund, Jennifer M.
Afiliación
  • Graham JB; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Swarts JL; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Wilkins C; Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Thomas S; Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Green R; Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Sekine A; Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Voss KM; Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Ireton RC; Center for Innate Immunity and Immune Disease, Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Mooney M; Division of Bioinformatics & Computational Biology, Department of Medical Informatics & Clinical Epidemiology, Oregon Health & Science University, Portland, Oregon, United States of America.
  • Choonoo G; OHSU Knight Cancer Center Institute, Oregon Health & Science University, Portland, Oregon, United States of America.
  • Miller DR; Division of Bioinformatics & Computational Biology, Department of Medical Informatics & Clinical Epidemiology, Oregon Health & Science University, Portland, Oregon, United States of America.
  • Treuting PM; OHSU Knight Cancer Center Institute, Oregon Health & Science University, Portland, Oregon, United States of America.
  • Pardo Manuel de Villena F; Lineberger Comprehensive Cancer Center, Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Ferris MT; Department of Comparative Medicine, University of Washington, Seattle, Washington, United States of America.
  • McWeeney S; Lineberger Comprehensive Cancer Center, Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Gale M; Lineberger Comprehensive Cancer Center, Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
  • Lund JM; Division of Bioinformatics & Computational Biology, Department of Medical Informatics & Clinical Epidemiology, Oregon Health & Science University, Portland, Oregon, United States of America.
PLoS Pathog ; 12(11): e1005996, 2016 Nov.
Article en En | MEDLINE | ID: mdl-27806117
ABSTRACT
Infection with West Nile virus (WNV) leads to a range of disease outcomes, including chronic infection, though lack of a robust mouse model of chronic WNV infection has precluded identification of the immune events contributing to persistent infection. Using the Collaborative Cross, a population of recombinant inbred mouse strains with high levels of standing genetic variation, we have identified a mouse model of persistent WNV disease, with persistence of viral loads within the brain. Compared to lines exhibiting no disease or marked disease, the F1 cross CC(032x013)F1 displays a strong immunoregulatory signature upon infection that correlates with restraint of the WNV-directed cytolytic response. We hypothesize that this regulatory T cell response sufficiently restrains the immune response such that a chronic infection can be maintained in the CNS. Use of this new mouse model of chronic neuroinvasive virus will be critical in developing improved strategies to prevent prolonged disease in humans.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fiebre del Nilo Occidental / Linfocitos T Reguladores Límite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Pathog Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fiebre del Nilo Occidental / Linfocitos T Reguladores Límite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Pathog Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos