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Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder

Mice of the low leukemia (BALB/cJ x A/J)F1 hybrid (CAF1) strain express B-and N-tropic infectious murine leukemia virus (MuLV) after the age of 6 mo. Initation of a protracted immunological disorder, the graft- versus-host reaction (GVHR), at 7 wk of age, accelerates the induction of both these mous...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1977
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180637/
https://www.ncbi.nlm.nih.gov/pubmed/16072
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description Mice of the low leukemia (BALB/cJ x A/J)F1 hybrid (CAF1) strain express B-and N-tropic infectious murine leukemia virus (MuLV) after the age of 6 mo. Initation of a protracted immunological disorder, the graft- versus-host reaction (GVHR), at 7 wk of age, accelerates the induction of both these mouse-tropic endogenous viruses, and preferentially enhances the replication of B-tropic MuLV. The earlier appearance of B- tropic MuLV in a greater proportion of mice and in higher titer is thought to be casually related to the eventual development of lymphoreticular tumors in the GVHR mice, since previous studies have shown that these same tumors can be reproduced by inoculating syngeneic recipients with serially passaged GVHR extracts containing B-tropic MuLV.
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spelling pubmed-21806372008-04-17 Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder J Exp Med Articles Mice of the low leukemia (BALB/cJ x A/J)F1 hybrid (CAF1) strain express B-and N-tropic infectious murine leukemia virus (MuLV) after the age of 6 mo. Initation of a protracted immunological disorder, the graft- versus-host reaction (GVHR), at 7 wk of age, accelerates the induction of both these mouse-tropic endogenous viruses, and preferentially enhances the replication of B-tropic MuLV. The earlier appearance of B- tropic MuLV in a greater proportion of mice and in higher titer is thought to be casually related to the eventual development of lymphoreticular tumors in the GVHR mice, since previous studies have shown that these same tumors can be reproduced by inoculating syngeneic recipients with serially passaged GVHR extracts containing B-tropic MuLV. The Rockefeller University Press 1977-04-01 /pmc/articles/PMC2180637/ /pubmed/16072 Text en 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 Articles
Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
title Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
title_full Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
title_fullStr Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
title_full_unstemmed Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
title_short Expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
title_sort expression of endogenous murine leukemia viruses during the course of a protracted immunological disorder
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180637/
https://www.ncbi.nlm.nih.gov/pubmed/16072