Nucleotide Oligomerization Binding Domain-Like Receptor Signaling Enhances Dendritic Cell-Mediated Cross-Priming In Vivo

被引:35
作者
Asano, Jumpei [2 ]
Tada, Hiroyuki [2 ]
Onai, Nobuyuki [2 ,4 ]
Sato, Taku [2 ,4 ]
Horie, Yasuo [3 ]
Fujimoto, Yukari [5 ]
Fukase, Koichi [5 ]
Suzuki, Akira [6 ]
Mak, Tak W. [7 ]
Ohteki, Toshiaki [1 ,2 ,4 ]
机构
[1] Tokyo Med & Dent Univ, Med Res Inst, Dept Biodef Res, Chiyoda Ku, Tokyo 1010062, Japan
[2] Akita Univ, Grad Sch Med, Dept Immunol, Akita 010, Japan
[3] Akita Univ, Grad Sch Med, Dept Gastroenterol, Akita 010, Japan
[4] Japan Sci & Technol Agcy, Core Res Evolut Sci & Technol, Tokyo, Japan
[5] Osaka Univ, Grad Sch Sci, Dept Chem, Osaka, Japan
[6] Kyushu Univ, Med Inst Bioregulat, Dept Mol Genet, Fukuoka 812, Japan
[7] Univ Toronto, Campbell Family Inst Breast Canc Res, Toronto, ON, Canada
基金
日本科学技术振兴机构;
关键词
CD8(+) T-CELLS; NF-KAPPA-B; ADAPTIVE IMMUNITY; BACTERIAL PEPTIDOGLYCAN; HOST RECOGNITION; ANTIGEN CAPTURE; INNATE; NOD1; ACTIVATION; RESPONSES;
D O I
10.4049/jimmunol.0900726
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nucleotide oligomerization binding domain (Nod)-like receptors are critical cytosolic sensors for the recognition of bacterial peptidoglycan. However, their role in the induction of dendritic cell (DC)-mediated cross-priming remains unclear. In this study, we demonstrate that injecting ligands for Nod1 and Nod2 along with Ag into wild-type mice significantly enhanced the cross-priming of Ag-specific CD8(+) T cells by CD8 alpha(+) DCs, as assessed from the expansion of IFN-gamma(+) CD8(+) T cells, CTL activity against Ag-pulsed targets, and the rejection of transplanted tumors expressing the cognate Ag. The enhancement of CD8 alpha(+) DC-mediated cross-priming was likely due to the upregulation of Ag cross-presentation and of costimulatory molecules. Our findings collectively indicate that Nod1/2 signaling is critical for the optimal induction of DC cross-priming in vivo, which may offer an alternative therapeutic pathway in cancer and hosts refractory to TLR signals or paralyzed by viral evasion strategy. The Journal of Immunology, 2010,184: 736-745.
引用
收藏
页码:736 / 745
页数:10
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