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Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing
We examined the ability of a set of cloned chicken ovalbumin (cOVA)- specific, Id-restricted, T cell hybridomas to produce interleukin-2 in response to cOVA presented by the Ia+ B cell lymphoma line, A20-2J. Although viable A20-2J cells presented native, denatured, and fragmented cOVA more or less e...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1983
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187345/ https://www.ncbi.nlm.nih.gov/pubmed/6193218 |
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collection | PubMed |
description | We examined the ability of a set of cloned chicken ovalbumin (cOVA)- specific, Id-restricted, T cell hybridomas to produce interleukin-2 in response to cOVA presented by the Ia+ B cell lymphoma line, A20-2J. Although viable A20-2J cells presented native, denatured, and fragmented cOVA more or less equally well, A20-2J cells that were glutaraldehyde-fixed could present only enzymatically or chemically fragmented cOVA. These results suggest that antigen fragmentation may be both necessary and sufficient to define accessory cell processing of soluble antigens so that they may be recognized in association with I- region molecules by T cells. |
format | Text |
id | pubmed-2187345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1983 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21873452008-04-17 Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing J Exp Med Articles We examined the ability of a set of cloned chicken ovalbumin (cOVA)- specific, Id-restricted, T cell hybridomas to produce interleukin-2 in response to cOVA presented by the Ia+ B cell lymphoma line, A20-2J. Although viable A20-2J cells presented native, denatured, and fragmented cOVA more or less equally well, A20-2J cells that were glutaraldehyde-fixed could present only enzymatically or chemically fragmented cOVA. These results suggest that antigen fragmentation may be both necessary and sufficient to define accessory cell processing of soluble antigens so that they may be recognized in association with I- region molecules by T cells. The Rockefeller University Press 1983-08-01 /pmc/articles/PMC2187345/ /pubmed/6193218 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 Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing |
title | Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing |
title_full | Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing |
title_fullStr | Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing |
title_full_unstemmed | Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing |
title_short | Antigen recognition by H-2-restricted T cells. I. Cell-free antigen processing |
title_sort | antigen recognition by h-2-restricted t cells. i. cell-free antigen processing |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187345/ https://www.ncbi.nlm.nih.gov/pubmed/6193218 |