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Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis

Mice infected with the coronavirus mouse hepatitis virus, strain JHM (JHM) develop a disease that shares many histological characteristics with multiple sclerosis. We previously demonstrated that JHM-infected mice that only have CD8 T cells specific for an epitope not in the virus develop demyelinat...

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Detalles Bibliográficos
Autores principales: Dandekar, Ajai A., Anghelina, Daniela, Perlman, Stanley
Formato: Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1602263/
https://www.ncbi.nlm.nih.gov/pubmed/14742242
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author Dandekar, Ajai A.
Anghelina, Daniela
Perlman, Stanley
author_facet Dandekar, Ajai A.
Anghelina, Daniela
Perlman, Stanley
author_sort Dandekar, Ajai A.
collection PubMed
description Mice infected with the coronavirus mouse hepatitis virus, strain JHM (JHM) develop a disease that shares many histological characteristics with multiple sclerosis. We previously demonstrated that JHM-infected mice that only have CD8 T cells specific for an epitope not in the virus develop demyelination on specific activation of these cells. Herein we show that this process of bystander T-cell-mediated demyelination is interferon-γ (IFN-γ)-dependent. The absence of IFN-γ abrogated demyelination but did not change T-cell infiltration or expression levels of inflammatory cytokines or chemokines in the spinal cord. These results are consistent with models in which IFN-γ contributes to CD8 T-cell-mediated demyelination by activation of macrophages/microglia, the final effector cells in the disease process.
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spelling pubmed-16022632007-03-26 Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis Dandekar, Ajai A. Anghelina, Daniela Perlman, Stanley Am J Pathol Short Communication Mice infected with the coronavirus mouse hepatitis virus, strain JHM (JHM) develop a disease that shares many histological characteristics with multiple sclerosis. We previously demonstrated that JHM-infected mice that only have CD8 T cells specific for an epitope not in the virus develop demyelination on specific activation of these cells. Herein we show that this process of bystander T-cell-mediated demyelination is interferon-γ (IFN-γ)-dependent. The absence of IFN-γ abrogated demyelination but did not change T-cell infiltration or expression levels of inflammatory cytokines or chemokines in the spinal cord. These results are consistent with models in which IFN-γ contributes to CD8 T-cell-mediated demyelination by activation of macrophages/microglia, the final effector cells in the disease process. American Society for Investigative Pathology 2004-02 /pmc/articles/PMC1602263/ /pubmed/14742242 Text en Copyright © American Society for Investigative Pathology
spellingShingle Short Communication
Dandekar, Ajai A.
Anghelina, Daniela
Perlman, Stanley
Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis
title Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis
title_full Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis
title_fullStr Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis
title_full_unstemmed Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis
title_short Bystander CD8 T-Cell-Mediated Demyelination is Interferon-γ-Dependent in a Coronavirus Model of Multiple Sclerosis
title_sort bystander cd8 t-cell-mediated demyelination is interferon-γ-dependent in a coronavirus model of multiple sclerosis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1602263/
https://www.ncbi.nlm.nih.gov/pubmed/14742242
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