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Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes

Studies have been performed on in vitro infection by Epstein-Barr virus (EBV) of subpopulations of human lymphocytes. B cells of adult peripheral or fetal cord blood transform with equal efficiency, whether assayed by DNA synthesis induction or by outgrowth of transformed lymphocytes. In contrast, u...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1977
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180764/
https://www.ncbi.nlm.nih.gov/pubmed/195004
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description Studies have been performed on in vitro infection by Epstein-Barr virus (EBV) of subpopulations of human lymphocytes. B cells of adult peripheral or fetal cord blood transform with equal efficiency, whether assayed by DNA synthesis induction or by outgrowth of transformed lymphocytes. In contrast, unfractionated adult lymphocytes transform much less efficiently than those from fetal cord. Reconstitution experiments of different cell preparations indicated that this difference was due to a suppression of B-cell proliferation by adult Ig- negative lymphocytes which fetal Ig-negative lymphocytes were unable to perform. Separation of Ig-negative lymphocytes into various subpopulations revealed that the suppression was performed by T cells. Macrophages and null cells play little or no role in suppression. The relevance of this phenomenon to infection and recovery from EBV infection during and after infectious mononucleosis is discussed.
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spelling pubmed-21807642008-04-17 Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes J Exp Med Articles Studies have been performed on in vitro infection by Epstein-Barr virus (EBV) of subpopulations of human lymphocytes. B cells of adult peripheral or fetal cord blood transform with equal efficiency, whether assayed by DNA synthesis induction or by outgrowth of transformed lymphocytes. In contrast, unfractionated adult lymphocytes transform much less efficiently than those from fetal cord. Reconstitution experiments of different cell preparations indicated that this difference was due to a suppression of B-cell proliferation by adult Ig- negative lymphocytes which fetal Ig-negative lymphocytes were unable to perform. Separation of Ig-negative lymphocytes into various subpopulations revealed that the suppression was performed by T cells. Macrophages and null cells play little or no role in suppression. The relevance of this phenomenon to infection and recovery from EBV infection during and after infectious mononucleosis is discussed. The Rockefeller University Press 1977-08-01 /pmc/articles/PMC2180764/ /pubmed/195004 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
Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes
title Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes
title_full Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes
title_fullStr Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes
title_full_unstemmed Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes
title_short Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes
title_sort suppression of in vitro epstein-barr virus infection. a new role for adult human t lymphocytes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180764/
https://www.ncbi.nlm.nih.gov/pubmed/195004