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.
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21 April 2003
Article|
April 14 2003
Complementary Role of CD4+ T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8+ T Cells
Ping Yu,
Ping Yu
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
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Michael T. Spiotto,
Michael T. Spiotto
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
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Youjin Lee,
Youjin Lee
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
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Hans Schreiber,
Hans Schreiber
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
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Yang-Xin Fu
Yang-Xin Fu
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
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Ping Yu
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
Michael T. Spiotto
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
Youjin Lee
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
Hans Schreiber
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
Yang-Xin Fu
Department of Pathology, Committee on Immunology, The University of Chicago, Chicago, IL 60637
Address correspondence to Yang-Xin Fu, Dept. of Pathology, MC3083, 5841 S. Maryland, The University of Chicago, Chicago, IL 60637. Phone: 773-702-0929; Fax: 773-834-8940; E-mail: [email protected]
*
Abbreviations used in this paper: BM, bone marrow; CFSE, carboxyfluorescein diacetate succinimidyl ester; CTL, cytolytic T lymphocytes; DC, dendritic cells; DLN, draining LN; LN, lymph node; LT, lymphotoxin; LTβR-Ig, LTβ receptor-Ig; NDLN, nondraining lymph node; SIY, SIYRYYGL; TNFR55-Ig, TNF receptor-Ig; WT, wild-type.
Received:
October 14 2002
Revision Received:
December 12 2002
Accepted:
February 21 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2003
J Exp Med (2003) 197 (8): 985–995.
Article history
Received:
October 14 2002
Revision Received:
December 12 2002
Accepted:
February 21 2003
Citation
Ping Yu, Michael T. Spiotto, Youjin Lee, Hans Schreiber, Yang-Xin Fu; Complementary Role of CD4+ T Cells and Secondary Lymphoid Tissues for Cross-presentation of Tumor Antigen to CD8+ T Cells . J Exp Med 21 April 2003; 197 (8): 985–995. doi: https://doi.org/10.1084/jem.20021804
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