CD103- and CD103+ bronchial lymph node dendritic cells are specialized in presenting and cross-presenting innocuous antigen to CD4+ and CD8+ T cells

被引:248
作者
del Rio, Maria-Luisa
Rodriguez-Barbosa, Jose-Ignacio
Kremmer, Elisabeth
Foerster, Reinhold
机构
[1] Hannover Med Sch, Inst Immunol, D-30625 Hannover, Germany
[2] Natl Res Ctr, Inst Mol Immunol, Munich, Germany
关键词
D O I
10.4049/jimmunol.178.11.6861
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Dendritic cells (DC) are able to capture, process, and present exogenous Ag to CD8(+) T lymphocytes through MHC class 1, a process referred to as cross-presentation. In this study, we demonstrate that CD103(+) (CD11c(high) CD11b(low)) and CD103(-)(CD11c(int)CD11b (high)) DC residing in the lung-draining bronchial lymph node (brLN) have evolved to acquire opposing functions in presenting innocuous inhaled Ag. Thus, under tolerogenic conditions, CD103(-) DC are specialized in presenting innocuous Ag to CD4(+) T cells, whereas CD103(+) DC, which do not express CD8 alpha, are specialized in presenting Ag exclusively to CD8(+) T cells. In CCR7-deficient but not in plt/plt mice, Ag-carrying CD103(+) DC are largely absent in the brLN, although CD103(+) DC are present in the lung of CCR7-deficient mice. As a consequence, adoptively transferred CD8(+) T cells can be activated under tolerizing conditions in plt/plt but not in CCR7-deficient mice. These data reveal that CD103(+) brLN DC are specialized in cross-presenting innocuous inhaled Ag in vivo. Because these cells are largely absent in CCR7(-/-) mice, our findings strongly suggest that brLN CD103(+) DC are lung-derived and that expression of CCR7 is required for their migration from the lung into its draining lymph node.
引用
收藏
页码:6861 / 6866
页数:6
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