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Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus

Infection of mice with the JHM strain of mouse hepatitis virus (MHV) results in an acute encephalomyelitis associated with primary demyelination of the central nervous system. Efforts at understanding the components of the immune response in the development of chronic MHV-induced demyelination have...

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Autores principales: Astohlman, Stephen, Kyuwaj, Shigeru, Cohen, Michael, Bergmann, Cornelia, Polo, John M., Yeh, Jason, Anthony, Richard, Keck, James G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131058/
https://www.ncbi.nlm.nih.gov/pubmed/1376538
http://dx.doi.org/10.1016/0042-6822(92)90697-N
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author Astohlman, Stephen
Kyuwaj, Shigeru
Cohen, Michael
Bergmann, Cornelia
Polo, John M.
Yeh, Jason
Anthony, Richard
Keck, James G.
author_facet Astohlman, Stephen
Kyuwaj, Shigeru
Cohen, Michael
Bergmann, Cornelia
Polo, John M.
Yeh, Jason
Anthony, Richard
Keck, James G.
author_sort Astohlman, Stephen
collection PubMed
description Infection of mice with the JHM strain of mouse hepatitis virus (MHV) results in an acute encephalomyelitis associated with primary demyelination of the central nervous system. Efforts at understanding the components of the immune response in the development of chronic MHV-induced demyelination have implicated the antibody response and both the CD4(+) and CD8(+) T cell responses. In this report, we demonstrate that Balb/c (H-2°) mice immunized with the JHM (JHMV) strain of MHV develop a CD8(+) cytotoxic T lymphocyte (CTL) response. One population of these virus-specific CTL recognize the nucleocapsid (N) protein. Recombinant vaccinia viruses expressing either the entire N protein or carboxy-terminal deletions were used to determine the number and location of the epitope(s) recognized. The CTLs were found to recognize a peptide contained within the carboxy-terminal 149 amino acids of the N protein. Analysis of infected cell lines expressing transfected major histocompatibility genes demonstrated that the anti-N protein CTLs were restricted exclusively to the L° molecule. These data provide the first definition of a MHV-specific CTL response directed to a viral protein and suggest that the anti-N protein CTL response is one potential mechanism used by the host to clear JHMV from the central nervous system.
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spelling pubmed-71310582020-04-08 Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus Astohlman, Stephen Kyuwaj, Shigeru Cohen, Michael Bergmann, Cornelia Polo, John M. Yeh, Jason Anthony, Richard Keck, James G. Virology Article Infection of mice with the JHM strain of mouse hepatitis virus (MHV) results in an acute encephalomyelitis associated with primary demyelination of the central nervous system. Efforts at understanding the components of the immune response in the development of chronic MHV-induced demyelination have implicated the antibody response and both the CD4(+) and CD8(+) T cell responses. In this report, we demonstrate that Balb/c (H-2°) mice immunized with the JHM (JHMV) strain of MHV develop a CD8(+) cytotoxic T lymphocyte (CTL) response. One population of these virus-specific CTL recognize the nucleocapsid (N) protein. Recombinant vaccinia viruses expressing either the entire N protein or carboxy-terminal deletions were used to determine the number and location of the epitope(s) recognized. The CTLs were found to recognize a peptide contained within the carboxy-terminal 149 amino acids of the N protein. Analysis of infected cell lines expressing transfected major histocompatibility genes demonstrated that the anti-N protein CTLs were restricted exclusively to the L° molecule. These data provide the first definition of a MHV-specific CTL response directed to a viral protein and suggest that the anti-N protein CTL response is one potential mechanism used by the host to clear JHMV from the central nervous system. Published by Elsevier Inc. 1992-07 2004-02-11 /pmc/articles/PMC7131058/ /pubmed/1376538 http://dx.doi.org/10.1016/0042-6822(92)90697-N Text en Copyright © 1992 Published by Elsevier Inc. 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
Astohlman, Stephen
Kyuwaj, Shigeru
Cohen, Michael
Bergmann, Cornelia
Polo, John M.
Yeh, Jason
Anthony, Richard
Keck, James G.
Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus
title Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus
title_full Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus
title_fullStr Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus
title_full_unstemmed Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus
title_short Mouse hepatitis virus nucleocapsid protein-specific cytotoxic T lymphocytes are L(d) restricted and specific for the carboxy terminus
title_sort mouse hepatitis virus nucleocapsid protein-specific cytotoxic t lymphocytes are l(d) restricted and specific for the carboxy terminus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131058/
https://www.ncbi.nlm.nih.gov/pubmed/1376538
http://dx.doi.org/10.1016/0042-6822(92)90697-N
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