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SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS

The viral-induced perivascular inflammatory response in Sindbis virus encephalitis of mice was shown to be immunologically specific. Mice were inoculated intracerebrally with Sindbis virus, and 24 hr later a single dose of cyclophosphamide was given which ablated the inflammatory response. 3 days af...

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Detalles Bibliográficos
Autores principales: McFarland, Henry F., Griffin, Diane E., Johnson, Richard T.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139202/
https://www.ncbi.nlm.nih.gov/pubmed/5043410
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author McFarland, Henry F.
Griffin, Diane E.
Johnson, Richard T.
author_facet McFarland, Henry F.
Griffin, Diane E.
Johnson, Richard T.
author_sort McFarland, Henry F.
collection PubMed
description The viral-induced perivascular inflammatory response in Sindbis virus encephalitis of mice was shown to be immunologically specific. Mice were inoculated intracerebrally with Sindbis virus, and 24 hr later a single dose of cyclophosphamide was given which ablated the inflammatory response. 3 days after virus inoculation, cells and/or sera from specifically and nonspecifically sensitized donor mice were given, and the inflammatory reactions, virus content, and antibody response of recipients were examined 5 days later. Reconstitution of the viral inflammatory response required virus-specific sensitized lymph node cells and was enhanced when these lymph node cells were combined with bone marrow cells. Reconstitution was not achieved with Sindbis virus immune serum even when combined with nonspecifically sensitized cells. Combination of immune serum with Sindbis virus-sensitized cells did not produce an accentuation of the reaction. In distinction, reconstitution of the inflammatory reaction surrounding the stab wound was reconstituted with bone marrow cells from mice inoculated with Sindbis virus or control antigens. Reconstitution of the perivascular reaction was associated with a reduction in brain virus content. Although the transfer of Sindbis virus-sensitized lymph node cells and bone marrow cells resulted in the limited production of neutralizing antibody in the immunosuppressed recipient, the reduction in virus was significantly greater with the transfers of Sindbis virus-sensitized lymph node cells than with the passive transfer of immune serum alone.
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spelling pubmed-21392022008-04-17 SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS McFarland, Henry F. Griffin, Diane E. Johnson, Richard T. J Exp Med Article The viral-induced perivascular inflammatory response in Sindbis virus encephalitis of mice was shown to be immunologically specific. Mice were inoculated intracerebrally with Sindbis virus, and 24 hr later a single dose of cyclophosphamide was given which ablated the inflammatory response. 3 days after virus inoculation, cells and/or sera from specifically and nonspecifically sensitized donor mice were given, and the inflammatory reactions, virus content, and antibody response of recipients were examined 5 days later. Reconstitution of the viral inflammatory response required virus-specific sensitized lymph node cells and was enhanced when these lymph node cells were combined with bone marrow cells. Reconstitution was not achieved with Sindbis virus immune serum even when combined with nonspecifically sensitized cells. Combination of immune serum with Sindbis virus-sensitized cells did not produce an accentuation of the reaction. In distinction, reconstitution of the inflammatory reaction surrounding the stab wound was reconstituted with bone marrow cells from mice inoculated with Sindbis virus or control antigens. Reconstitution of the perivascular reaction was associated with a reduction in brain virus content. Although the transfer of Sindbis virus-sensitized lymph node cells and bone marrow cells resulted in the limited production of neutralizing antibody in the immunosuppressed recipient, the reduction in virus was significantly greater with the transfers of Sindbis virus-sensitized lymph node cells than with the passive transfer of immune serum alone. The Rockefeller University Press 1972-08-01 /pmc/articles/PMC2139202/ /pubmed/5043410 Text en Copyright © 1972 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
McFarland, Henry F.
Griffin, Diane E.
Johnson, Richard T.
SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS
title SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS
title_full SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS
title_fullStr SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS
title_full_unstemmed SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS
title_short SPECIFICITY OF THE INFLAMMATORY RESPONSE IN VIRAL ENCEPHALITIS : I. ADOPTIVE IMMUNIZATION OF IMMUNOSUPPRESSED MICE INFECTED WITH SINDBIS VIRUS
title_sort specificity of the inflammatory response in viral encephalitis : i. adoptive immunization of immunosuppressed mice infected with sindbis virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139202/
https://www.ncbi.nlm.nih.gov/pubmed/5043410
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