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Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors

Evidence is presented for the selective suppression of the major idiotypic component of the humoral response to the phenylarsonate hapten by soluble factors derived from T cells (TsF). The existence of TsF with anti-idiotypic receptors was also demonstrated. It was found that TsF with idiotypic and...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1980
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185863/
https://www.ncbi.nlm.nih.gov/pubmed/6966320
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description Evidence is presented for the selective suppression of the major idiotypic component of the humoral response to the phenylarsonate hapten by soluble factors derived from T cells (TsF). The existence of TsF with anti-idiotypic receptors was also demonstrated. It was found that TsF with idiotypic and anti-idiotypic receptors coexist in cultures of spleen cells prepared from idiotypically suppressed, hyperimmunized mice. By gel filtration the molecular weight of each factor was found to be 50,000-100,000. Each is sensitive to trypsin and is bound to a column containing anti-H-2a antibodies. Evidence is discussed which suggests the possibility of mutual stimulation of suppressor T cells with idiotypic and anti-idiotypic receptors.
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spelling pubmed-21858632008-04-17 Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors J Exp Med Articles Evidence is presented for the selective suppression of the major idiotypic component of the humoral response to the phenylarsonate hapten by soluble factors derived from T cells (TsF). The existence of TsF with anti-idiotypic receptors was also demonstrated. It was found that TsF with idiotypic and anti-idiotypic receptors coexist in cultures of spleen cells prepared from idiotypically suppressed, hyperimmunized mice. By gel filtration the molecular weight of each factor was found to be 50,000-100,000. Each is sensitive to trypsin and is bound to a column containing anti-H-2a antibodies. Evidence is discussed which suggests the possibility of mutual stimulation of suppressor T cells with idiotypic and anti-idiotypic receptors. The Rockefeller University Press 1980-05-01 /pmc/articles/PMC2185863/ /pubmed/6966320 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
Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors
title Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors
title_full Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors
title_fullStr Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors
title_full_unstemmed Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors
title_short Selective suppression of the major idiotypic component of an antihapten response by soluble T cell-derived factors with idiotypic or anti- idiotypic receptors
title_sort selective suppression of the major idiotypic component of an antihapten response by soluble t cell-derived factors with idiotypic or anti- idiotypic receptors
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185863/
https://www.ncbi.nlm.nih.gov/pubmed/6966320