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Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens
Activated CTL can kill any cell to which they bind or by which they are bound. This observation has been used to determine whether alloreactive CTL can recognize cells bearing self-MHC. When activated by their specific targets, 19 CTL clones of 4 different specificities and origins killed bystander...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1989
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189386/ https://www.ncbi.nlm.nih.gov/pubmed/2787386 |
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collection | PubMed |
description | Activated CTL can kill any cell to which they bind or by which they are bound. This observation has been used to determine whether alloreactive CTL can recognize cells bearing self-MHC. When activated by their specific targets, 19 CTL clones of 4 different specificities and origins killed bystander targets bearing syngeneic but not third-party MHC antigens. Using target cells derived from MHC-recombinant animals, syngeneic bystander killing was shown to be restricted to a single self MHC-encoded molecule. These results provide the first clear demonstration that T cells, or more precisely CTL, are capable of self recognition in the absence of their specific antigen. Our findings support the model that T cell repertoire selection occurs as a result of positive selection during maturation in the thymus of precursor cells whose antigen receptors have low but real affinity for self-MHC. |
format | Text |
id | pubmed-2189386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21893862008-04-17 Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens J Exp Med Articles Activated CTL can kill any cell to which they bind or by which they are bound. This observation has been used to determine whether alloreactive CTL can recognize cells bearing self-MHC. When activated by their specific targets, 19 CTL clones of 4 different specificities and origins killed bystander targets bearing syngeneic but not third-party MHC antigens. Using target cells derived from MHC-recombinant animals, syngeneic bystander killing was shown to be restricted to a single self MHC-encoded molecule. These results provide the first clear demonstration that T cells, or more precisely CTL, are capable of self recognition in the absence of their specific antigen. Our findings support the model that T cell repertoire selection occurs as a result of positive selection during maturation in the thymus of precursor cells whose antigen receptors have low but real affinity for self-MHC. The Rockefeller University Press 1989-07-01 /pmc/articles/PMC2189386/ /pubmed/2787386 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 Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens |
title | Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens |
title_full | Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens |
title_fullStr | Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens |
title_full_unstemmed | Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens |
title_short | Self recognition by T cells. I. Bystander killing of target cells bearing syngeneic MHC antigens |
title_sort | self recognition by t cells. i. bystander killing of target cells bearing syngeneic mhc antigens |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189386/ https://www.ncbi.nlm.nih.gov/pubmed/2787386 |