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B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens

Murine mammary tumor viruses (MMTVs) are retroviruses that encode superantigens capable of stimulating T cells via superantigen-reactive T cell receptor V beta chains. MMTVs are transmitted to the suckling offspring through milk. Here we show that B cell-deficient mice foster nursed by virus-secreti...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191484/
https://www.ncbi.nlm.nih.gov/pubmed/8163931
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collection PubMed
description Murine mammary tumor viruses (MMTVs) are retroviruses that encode superantigens capable of stimulating T cells via superantigen-reactive T cell receptor V beta chains. MMTVs are transmitted to the suckling offspring through milk. Here we show that B cell-deficient mice foster nursed by virus-secreting mice do not transfer infectious MMTVs to their offspring. No MMTV proviruses could be detected in the spleen and mammary tissue of these mice, and no deletion of MMTV superantigen- reactive T cells occurred. By contrast, T cell deletion and positive selection due to endogenous MMTV superantigens occurred in B cell- deficient mice. We conclude that B cells are essential for the completion of the viral life cycle in vivo, but that endogenous MMTV superantigens can be presented by cell types other than B cells.
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spelling pubmed-21914842008-04-16 B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens J Exp Med Articles Murine mammary tumor viruses (MMTVs) are retroviruses that encode superantigens capable of stimulating T cells via superantigen-reactive T cell receptor V beta chains. MMTVs are transmitted to the suckling offspring through milk. Here we show that B cell-deficient mice foster nursed by virus-secreting mice do not transfer infectious MMTVs to their offspring. No MMTV proviruses could be detected in the spleen and mammary tissue of these mice, and no deletion of MMTV superantigen- reactive T cells occurred. By contrast, T cell deletion and positive selection due to endogenous MMTV superantigens occurred in B cell- deficient mice. We conclude that B cells are essential for the completion of the viral life cycle in vivo, but that endogenous MMTV superantigens can be presented by cell types other than B cells. The Rockefeller University Press 1994-05-01 /pmc/articles/PMC2191484/ /pubmed/8163931 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
B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
title B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
title_full B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
title_fullStr B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
title_full_unstemmed B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
title_short B cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
title_sort b cells are essential for murine mammary tumor virus transmission, but not for presentation of endogenous superantigens
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191484/
https://www.ncbi.nlm.nih.gov/pubmed/8163931