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Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help
Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation....
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198964/ https://www.ncbi.nlm.nih.gov/pubmed/9206998 |
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author | Bennett, Sally R.M. Carbone, Francis R. Karamalis, Freda Miller, Jacques F.A.P. Heath, William R. |
author_facet | Bennett, Sally R.M. Carbone, Francis R. Karamalis, Freda Miller, Jacques F.A.P. Heath, William R. |
author_sort | Bennett, Sally R.M. |
collection | PubMed |
description | Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation. This is known to be effective for class I–restricted cytotoxic T lymphocyte (CTL) cross-priming directed against a variety of exogenous tumor, viral, and minor transplantation antigens. The related effect of cross-tolerance can also effectively eliminate responses to selected self components. In both cases, this presentation appears to require the active involvement of a bone marrow–derived antigen presenting cell (APC). Here, we show that CTL induction by cross-priming with cell-associated ovalbumin requires the active involvement of CD4(+) helper T cells. Importantly, this CD4(+) population is only effective when both the helper and CTL determinants are recognized on the same APC. Moreover, we would argue that the cognitive nature of this event suggests that the CD4(+) T cell actively modifies the APC, converting it into an effective stimulator for the successful priming of the CTL precursor. |
format | Text |
id | pubmed-2198964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21989642008-04-16 Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help Bennett, Sally R.M. Carbone, Francis R. Karamalis, Freda Miller, Jacques F.A.P. Heath, William R. J Exp Med Article Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation. This is known to be effective for class I–restricted cytotoxic T lymphocyte (CTL) cross-priming directed against a variety of exogenous tumor, viral, and minor transplantation antigens. The related effect of cross-tolerance can also effectively eliminate responses to selected self components. In both cases, this presentation appears to require the active involvement of a bone marrow–derived antigen presenting cell (APC). Here, we show that CTL induction by cross-priming with cell-associated ovalbumin requires the active involvement of CD4(+) helper T cells. Importantly, this CD4(+) population is only effective when both the helper and CTL determinants are recognized on the same APC. Moreover, we would argue that the cognitive nature of this event suggests that the CD4(+) T cell actively modifies the APC, converting it into an effective stimulator for the successful priming of the CTL precursor. The Rockefeller University Press 1997-07-07 /pmc/articles/PMC2198964/ /pubmed/9206998 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 | Article Bennett, Sally R.M. Carbone, Francis R. Karamalis, Freda Miller, Jacques F.A.P. Heath, William R. Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help |
title | Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help |
title_full | Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help |
title_fullStr | Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help |
title_full_unstemmed | Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help |
title_short | Induction of a CD8(+) Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4(+) T Cell Help |
title_sort | induction of a cd8(+) cytotoxic t lymphocyte response by cross-priming requires cognate cd4(+) t cell help |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198964/ https://www.ncbi.nlm.nih.gov/pubmed/9206998 |
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