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Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors

Five hybridoma T cell lines were prepared by fusion of Ts3 cells with the BW 5147 thymoma. The culture supernatants from these T cell hybrids contained a factor, TsF3, which specifically suppressed 4-hydroxy-3- nitrophenyl acetyl hapten (NP(-hapten cutaneous sensitivity responses. The properties of...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1981
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186548/
https://www.ncbi.nlm.nih.gov/pubmed/6172534
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description Five hybridoma T cell lines were prepared by fusion of Ts3 cells with the BW 5147 thymoma. The culture supernatants from these T cell hybrids contained a factor, TsF3, which specifically suppressed 4-hydroxy-3- nitrophenyl acetyl hapten (NP(-hapten cutaneous sensitivity responses. The properties of this new series of hybridoma factors was compared with those of two previously characterized types of NP-specific suppressor factors (TsF1 and TsF2). TsF3 activity was only observed if the factor was administered during the effector phases of the immune response. TsF3 bears I-J and C57BL anti-NP antibody idiotypic determinants and has binding specificity for the NP hapten. Furthermore, TsF3 does not suppress H-2 (I-J)-incompatible mice. In addition to this H-2 restriction, the monoclonal TsF3 factors also demonstrated an Igh genetic restriction. Finally, the TsF3 factors could be distinguished by their ability to suppress cyclophosphamide- treated recipients.
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spelling pubmed-21865482008-04-17 Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors J Exp Med Articles Five hybridoma T cell lines were prepared by fusion of Ts3 cells with the BW 5147 thymoma. The culture supernatants from these T cell hybrids contained a factor, TsF3, which specifically suppressed 4-hydroxy-3- nitrophenyl acetyl hapten (NP(-hapten cutaneous sensitivity responses. The properties of this new series of hybridoma factors was compared with those of two previously characterized types of NP-specific suppressor factors (TsF1 and TsF2). TsF3 activity was only observed if the factor was administered during the effector phases of the immune response. TsF3 bears I-J and C57BL anti-NP antibody idiotypic determinants and has binding specificity for the NP hapten. Furthermore, TsF3 does not suppress H-2 (I-J)-incompatible mice. In addition to this H-2 restriction, the monoclonal TsF3 factors also demonstrated an Igh genetic restriction. Finally, the TsF3 factors could be distinguished by their ability to suppress cyclophosphamide- treated recipients. The Rockefeller University Press 1981-12-01 /pmc/articles/PMC2186548/ /pubmed/6172534 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
Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors
title Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors
title_full Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors
title_fullStr Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors
title_full_unstemmed Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors
title_short Analysis of T cell hybridomas. II. Comparisons among three distinct types of monoclonal suppressor factors
title_sort analysis of t cell hybridomas. ii. comparisons among three distinct types of monoclonal suppressor factors
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186548/
https://www.ncbi.nlm.nih.gov/pubmed/6172534