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Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals

Infection of mice with mouse hepatitis virus (MHV) strain A59 results in acute encephalitis, hepatitis, and chronic demyelinating disease. T lymphocytes play an important role in MHV infection, and costimulatory signals are an important component of T cell function. To elucidate the role of the main...

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Autores principales: Gonzales, Donna M, Fu, Li, Li, Yun, Das Sarma, Jayasri, Lavi, Ehud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier/North-Holland 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119462/
https://www.ncbi.nlm.nih.gov/pubmed/14698856
http://dx.doi.org/10.1016/j.jneuroim.2003.10.053
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author Gonzales, Donna M
Fu, Li
Li, Yun
Das Sarma, Jayasri
Lavi, Ehud
author_facet Gonzales, Donna M
Fu, Li
Li, Yun
Das Sarma, Jayasri
Lavi, Ehud
author_sort Gonzales, Donna M
collection PubMed
description Infection of mice with mouse hepatitis virus (MHV) strain A59 results in acute encephalitis, hepatitis, and chronic demyelinating disease. T lymphocytes play an important role in MHV infection, and costimulatory signals are an important component of T cell function. To elucidate the role of the main costimulatory molecule, CD28, in MHV pathogenesis and demyelination, we examined the kinetics of MHV-A59 infection in CD28 knockout mice. MHV-A59-infected CD28 knockout mice developed acute encephalitis and hepatitis, and the same degree of chronic demyelination as normal C57Bl/6 (B6) mice. Thus, CD28, the costimulatory T cell molecule, is not required for MHV infection and MHV-induced demyelination.
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spelling pubmed-71194622020-04-08 Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals Gonzales, Donna M Fu, Li Li, Yun Das Sarma, Jayasri Lavi, Ehud J Neuroimmunol Article Infection of mice with mouse hepatitis virus (MHV) strain A59 results in acute encephalitis, hepatitis, and chronic demyelinating disease. T lymphocytes play an important role in MHV infection, and costimulatory signals are an important component of T cell function. To elucidate the role of the main costimulatory molecule, CD28, in MHV pathogenesis and demyelination, we examined the kinetics of MHV-A59 infection in CD28 knockout mice. MHV-A59-infected CD28 knockout mice developed acute encephalitis and hepatitis, and the same degree of chronic demyelination as normal C57Bl/6 (B6) mice. Thus, CD28, the costimulatory T cell molecule, is not required for MHV infection and MHV-induced demyelination. Elsevier/North-Holland 2004-01 2003-12-22 /pmc/articles/PMC7119462/ /pubmed/14698856 http://dx.doi.org/10.1016/j.jneuroim.2003.10.053 Text en Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Gonzales, Donna M
Fu, Li
Li, Yun
Das Sarma, Jayasri
Lavi, Ehud
Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals
title Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals
title_full Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals
title_fullStr Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals
title_full_unstemmed Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals
title_short Coronavirus-induced demyelination occurs in the absence of CD28 costimulatory signals
title_sort coronavirus-induced demyelination occurs in the absence of cd28 costimulatory signals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119462/
https://www.ncbi.nlm.nih.gov/pubmed/14698856
http://dx.doi.org/10.1016/j.jneuroim.2003.10.053
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