Natural killer cells license dendritic cell cross-presentation of B lymphoma cell - Associated antigens

被引:14
作者
Dao, T [1 ]
Gomez-Nunez, M [1 ]
Antczak, C [1 ]
Kappel, B [1 ]
Jaggi, JS [1 ]
Korontsvit, T [1 ]
Zakhaleva, V [1 ]
Scheinberg, DA [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, New York, NY 10021 USA
关键词
D O I
10.1158/1078-0432.CCR-05-0975
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Presentation of exogenous antigen by MHC class I molecules, or cross-presentation, is a property of dendritic cells, which is considered crucial for the priming of cytotoxic T-cell response to tumor antigens. However, the precise mechanisms of this process are not fully understood, Experimental Design and Results: We show here in a human in vitro system, using B lymphoma cells as a tumor model, that the cross-presentation of cell-associated antigens to T cells by dendritic cells requires "help" from natural killer cells. When autologous dendritic cells that had taken up apoptotic B lymphoma cells and induced to a fully mature state were used to stimulate nonadherent cells of peripheral blood mononuclear cells from healthy donors, they induced strong cytotoxicity against B lymphoma cells in a HLA-A0201-restricted manner. The cells failed to induce cytotoxicity, however, when purified T cells were used as effector cells. Depletion of CD56(+) cells, but not CD14(+) or CD19(+) cells, abrogated the cytotoxicity of non- adherent cells, showing that the help was provided by natural killer cells. Further, when natural killer cells were present in the cultures, a strong and persistent production of interleukin-18, but not interleukin-12 and interleukin-15, was observed. Blocking interleukin-18 significantly reduced the cytotoxicity of nonadherent cells against B lymphoma cells. Conclusions: These results suggest that capture of tumor cells and a full maturation status of dendritic cells are not sufficient to cross-prime CD8 Tcells. Effective cross-priming requires further activation of dendritic cells by natural killer cells and an abundant production of interleukin-18, which, along with other yet undefined mechanisms, contribute to the generation of CTL response against B-cell lymphoma.
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收藏
页码:8763 / 8772
页数:10
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