Tumor antigen cross-presentation and the dendritic cell: where it all begins?
- PMID: 20976125
- PMCID: PMC2957101
- DOI: 10.1155/2010/539519
Tumor antigen cross-presentation and the dendritic cell: where it all begins?
Abstract
Dendritic cells (DCs) are professional antigen-presenting cells (APCs) that are critical for the generation of effective cytotoxic T lymphocyte (CTL) responses; however, their function and phenotype are often defective or altered in tumor-bearing hosts, which may limit their capacity to mount an effective tumor-specific CTL response. In particular, the manner in which exogenous tumor antigens are acquired, processed, and cross-presented to CD8 T cells by DCs in tumor-bearing hosts is not well understood, but may have a profound effect on antitumor immunity. In this paper, we have examined the role of DCs in the cross-presentation of tumor antigen in terms of their subset, function, migration, and location with the intention of examining the early processes that contribute to the development of an ineffective anti-tumor immune response.
References
-
- Ochsenbein AF, Sierro S, Odermatt B, et al. Roles of tumour localization, second signals and cross priming in cytotoxic T-cell induction. Nature. 2001;411(6841):1058–1064. - PubMed
-
- Zinkernagel RM. On cross-priming of MHC class I-specific CTL: rule or exception? European Journal of Immunology. 2002;32(9):2385–2392. - PubMed
-
- Boonman ZFHM, Van Mierlo GJD, Fransen MF, et al. Intraocular tumor antigen drains specifically to submandibular lymph nodes, resulting in an abortive cytotoxic T cell reaction. Journal of Immunology. 2004;172(3):1567–1574. - PubMed
-
- Huang AYC, Golumbek P, Ahmadzadeh M, Jaffee E, Pardoll D, Levitsky H. Role of bone marrow-derived cells in presenting MHC class I-restricted tumor antigens. Science. 1994;264(5161):961–965. - PubMed
-
- McDonnell AM, Prosser AC, van Bruggen I, et al. CD8alpha+ DC are not the sole subset cross-presenting cell-associated tumor antigens from a solid tumor. European Journal of Immunology. 2010;40(6):1617–1627. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous
