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Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice
A panel of DBA/2 T cell hybridomas specific for the sperm whale myoglobin epitope 110-121 was found to recognize antigen presented by the mixed isotype class II molecule E alpha dA beta d. The response was blocked by monoclonal antibodies specific for E alpha and A beta d chains; in addition, the hy...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1992
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119090/ https://www.ncbi.nlm.nih.gov/pubmed/1730914 |
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collection | PubMed |
description | A panel of DBA/2 T cell hybridomas specific for the sperm whale myoglobin epitope 110-121 was found to recognize antigen presented by the mixed isotype class II molecule E alpha dA beta d. The response was blocked by monoclonal antibodies specific for E alpha and A beta d chains; in addition, the hybridomas responded to antigen presented by L cells expressing E alpha A beta d molecules, and made no response with L cells expressing I-Ad or I-Ed molecules. Two more groups of hybridomas isolated from DBA/2 and B10.D2 mice immunized with myoglobin also recognized peptide 110-121 presented by E alpha d A beta d. Thus, although it is expressed at biochemically undetectable levels on spleen cells, the E alpha d A beta d molecule is an important presenting element in normal H-2d mice making a conventional immune response to a protein antigen. These results suggest that high levels of class II expression are not a prerequisite for T cell activation. |
format | Text |
id | pubmed-2119090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21190902008-04-16 Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice J Exp Med Articles A panel of DBA/2 T cell hybridomas specific for the sperm whale myoglobin epitope 110-121 was found to recognize antigen presented by the mixed isotype class II molecule E alpha dA beta d. The response was blocked by monoclonal antibodies specific for E alpha and A beta d chains; in addition, the hybridomas responded to antigen presented by L cells expressing E alpha A beta d molecules, and made no response with L cells expressing I-Ad or I-Ed molecules. Two more groups of hybridomas isolated from DBA/2 and B10.D2 mice immunized with myoglobin also recognized peptide 110-121 presented by E alpha d A beta d. Thus, although it is expressed at biochemically undetectable levels on spleen cells, the E alpha d A beta d molecule is an important presenting element in normal H-2d mice making a conventional immune response to a protein antigen. These results suggest that high levels of class II expression are not a prerequisite for T cell activation. The Rockefeller University Press 1992-01-01 /pmc/articles/PMC2119090/ /pubmed/1730914 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 Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice |
title | Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice |
title_full | Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice |
title_fullStr | Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice |
title_full_unstemmed | Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice |
title_short | Presentation of antigen by mixed isotype class II molecules in normal H- 2d mice |
title_sort | presentation of antigen by mixed isotype class ii molecules in normal h- 2d mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119090/ https://www.ncbi.nlm.nih.gov/pubmed/1730914 |