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Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help
We have investigated the induction of antibody responses to erythrocyte (RBC)-bound antigens in the (CBA/N x B10)F1 mouse. Male B cells, which express the CBA/N defect, were shown to be unresponsive to RBC antigens when the delivered T cell helper activity was solely nonspecific. Thus we demonstrate...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1981
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186522/ https://www.ncbi.nlm.nih.gov/pubmed/6975350 |
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collection | PubMed |
description | We have investigated the induction of antibody responses to erythrocyte (RBC)-bound antigens in the (CBA/N x B10)F1 mouse. Male B cells, which express the CBA/N defect, were shown to be unresponsive to RBC antigens when the delivered T cell helper activity was solely nonspecific. Thus we demonstrated that defective B cells did not respond to concanavalin A supernatants or bystander helper activity, in spite of the fact that CBA/N-defective mice could produce these T cell activities. The defective B cell did not respond to RBC-bound antigen in the presence of RBC-primed T cells, although the magnitude of this response was usually twofold less than normal controls. The insensitivity of CBA/N defective B cells to nonspecific T cell helper activities seemed to involve at least the inability of RBC antigens to activate defective B cells in the absence of antigen-specific T cell help. |
format | Text |
id | pubmed-2186522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1981 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21865222008-04-17 Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help J Exp Med Articles We have investigated the induction of antibody responses to erythrocyte (RBC)-bound antigens in the (CBA/N x B10)F1 mouse. Male B cells, which express the CBA/N defect, were shown to be unresponsive to RBC antigens when the delivered T cell helper activity was solely nonspecific. Thus we demonstrated that defective B cells did not respond to concanavalin A supernatants or bystander helper activity, in spite of the fact that CBA/N-defective mice could produce these T cell activities. The defective B cell did not respond to RBC-bound antigen in the presence of RBC-primed T cells, although the magnitude of this response was usually twofold less than normal controls. The insensitivity of CBA/N defective B cells to nonspecific T cell helper activities seemed to involve at least the inability of RBC antigens to activate defective B cells in the absence of antigen-specific T cell help. The Rockefeller University Press 1981-11-01 /pmc/articles/PMC2186522/ /pubmed/6975350 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 the response of B cells from CBA/N-defective mice to nonspecific T cell help |
title | Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help |
title_full | Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help |
title_fullStr | Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help |
title_full_unstemmed | Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help |
title_short | Analysis of the response of B cells from CBA/N-defective mice to nonspecific T cell help |
title_sort | analysis of the response of b cells from cba/n-defective mice to nonspecific t cell help |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186522/ https://www.ncbi.nlm.nih.gov/pubmed/6975350 |