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Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells
MHC class I–restricted tumor antigens can be presented to CD8(+) T cells by two distinct pathways: via direct and indirect presentation. The relative contribution of these two pathways toward the initial activation of tumor antigen–specific CD8(+) T cells and their subsequent tumor rejection is stil...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193872/ https://www.ncbi.nlm.nih.gov/pubmed/12695490 http://dx.doi.org/10.1084/jem.20021804 |
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author | Yu, Ping Spiotto, Michael T. Lee, Youjin Schreiber, Hans Fu, Yang-Xin |
author_facet | Yu, Ping Spiotto, Michael T. Lee, Youjin Schreiber, Hans Fu, Yang-Xin |
author_sort | Yu, Ping |
collection | PubMed |
description | MHC class I–restricted tumor antigens can be presented to CD8(+) T cells by two distinct pathways: via direct and indirect presentation. The relative contribution of these two pathways toward the initial activation of tumor antigen–specific CD8(+) T cells and their subsequent tumor rejection is still vigorously debated. Using a tumor model able to dissect the relative contributions of direct and indirect presentation, we show unequivocally the inefficiency of direct presentation and the essential requirement of indirect presentation for the priming of naive tumor antigen–specific T cells leading to tumor rejection. Moreover, we characterize the essential environment under which indirect presentation occurs, and find efficient cross-priming of tumor-specific CD8(+) T cells in the complete absence of secondary lymphoid tissues. The independence of this process from local lymph nodes is compromised, however, in the absence of CD4(+) T cell help. Therefore, our paper demonstrates that effective immune protection against tumors requires the cross-priming of CD8(+) T cells under conditions that require either CD4(+) T cell help, or draining lymph nodes. |
format | Text |
id | pubmed-2193872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21938722008-04-11 Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells Yu, Ping Spiotto, Michael T. Lee, Youjin Schreiber, Hans Fu, Yang-Xin J Exp Med Article MHC class I–restricted tumor antigens can be presented to CD8(+) T cells by two distinct pathways: via direct and indirect presentation. The relative contribution of these two pathways toward the initial activation of tumor antigen–specific CD8(+) T cells and their subsequent tumor rejection is still vigorously debated. Using a tumor model able to dissect the relative contributions of direct and indirect presentation, we show unequivocally the inefficiency of direct presentation and the essential requirement of indirect presentation for the priming of naive tumor antigen–specific T cells leading to tumor rejection. Moreover, we characterize the essential environment under which indirect presentation occurs, and find efficient cross-priming of tumor-specific CD8(+) T cells in the complete absence of secondary lymphoid tissues. The independence of this process from local lymph nodes is compromised, however, in the absence of CD4(+) T cell help. Therefore, our paper demonstrates that effective immune protection against tumors requires the cross-priming of CD8(+) T cells under conditions that require either CD4(+) T cell help, or draining lymph nodes. The Rockefeller University Press 2003-04-21 /pmc/articles/PMC2193872/ /pubmed/12695490 http://dx.doi.org/10.1084/jem.20021804 Text en Copyright © 2003, The Rockefeller University Press 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 Yu, Ping Spiotto, Michael T. Lee, Youjin Schreiber, Hans Fu, Yang-Xin Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells |
title | Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells |
title_full | Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells |
title_fullStr | Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells |
title_full_unstemmed | Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells |
title_short | Complementary Role of CD4(+) T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8(+) T Cells |
title_sort | complementary role of cd4(+) t cells and secondary lymphoid tissues for cross-presentation of tumor antigen to cd8(+) t cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193872/ https://www.ncbi.nlm.nih.gov/pubmed/12695490 http://dx.doi.org/10.1084/jem.20021804 |
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