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Genetic Variants and Immune Responses in a Cohort of Patients With Varicella Zoster Virus Encephalitis.
Thomsen, Michelle M; Tyrberg, Tobias; Skaalum, Kristoffer; Carter-Timofte, Madalina; Freytag, Mette R; Norberg, Peter; Helleberg, Marie; Storgaard, Merete; Nielsen, Henrik; Bodilsen, Jacob; Grahn, Anna; Mogensen, Trine H.
Afiliação
  • Thomsen MM; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Tyrberg T; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Skaalum K; Department of Infectious Diseases, Institute of Biomedicine, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Carter-Timofte M; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Freytag MR; Department of Biomedicine, Aarhus University, Aarhus, Denmark.
  • Norberg P; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Helleberg M; Department of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.
  • Storgaard M; Department of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.
  • Nielsen H; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Bodilsen J; Department of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.
  • Grahn A; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
  • Mogensen TH; Department of Infectious Diseases, Aalborg University Hospital, Aalborg, Denmark.
J Infect Dis ; 224(12): 2122-2132, 2021 12 15.
Article em En | MEDLINE | ID: mdl-33974706
BACKGROUND: Infection with varicella zoster virus (VZV) may involve different central nervous system (CNS) manifestations, including meningitis, encephalitis, and vasculitis. In cases in which otherwise healthy individuals are affected, an inborn error of immunity may underlie increased susceptibility or severity of infection. METHODS: We collected a cohort of 17 adults who experienced VZV encephalitis and performed whole exome sequencing. Patient peripheral blood mononuclear cells were infected with VZV, and innate antiviral interferon (IFN) and cytokine responses as well as viral replication were evaluated. Data were analyzed by Mann-Whitney U test. RESULTS: We identified a total of 21 different potentially disease-causing variants in a total of 13 of the 17 patients included. These gene variants were within 2 major functional clusters: (1) innate viral sensors and immune pathways and (2) autophagy pathways. Antiviral IFN and cytokine responses were abnormal in the majority of patients, whereas viral replication was increased in only 2 of 17 patients. CONCLUSIONS: This study identifies a list of variants of pathogenic potential, which may serve as a platform for generating hypotheses for future studies addressing genetic and immunological factors associated with susceptibility to VZV encephalitis. These data, taken together, suggest that disturbances in innate sensing and autophagy pathways may predispose to VZV encephalitis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citocinas / Herpesvirus Humano 3 / Encefalite por Varicela Zoster / Imunidade Inata Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Child, preschool / Humans / Middle aged Idioma: En Revista: J Infect Dis Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citocinas / Herpesvirus Humano 3 / Encefalite por Varicela Zoster / Imunidade Inata Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Child, preschool / Humans / Middle aged Idioma: En Revista: J Infect Dis Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Dinamarca