Dendritic cells directly trigger NK cell functions:: Cross-talk relevant in innate anti-tumor immune responses in vivo

被引:854
作者
Fernandez, NC
Lozier, A
Flament, C
Ricciardi-Castagnoli, P
Bellet, D
Suter, M
Perricaudet, M
Tursz, T
Maraskovsky, E
Zitvogel, L [1 ]
机构
[1] Inst Gustave Roussy, Dept Biol Clin, Unite Immunol, Villejuif, France
[2] Inst Gustave Roussy, CNRS, UMR1582, Villejuif, France
[3] Univ Milan, Dept Biotechnol & Biosci, Milan, Italy
[4] Univ Zurich, Inst Virol, Zurich, Switzerland
[5] Immunex Res & Dev Corp, Dept Immunobiol, Seattle, WA 98101 USA
[6] Repatriat Med Ctr, Heidelberg, Vic, Australia
[7] Ludwig Oncol Unit, Austin, Australia
关键词
D O I
10.1038/7403
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytotoxic T lymphocytes and natural killer cells are essential effecters of anti-tumor immune responses in vivo. Dendritic cells (DC) 'prime' tumor antigen-specific cytotoxic T lymphocytes; thus, we investigated whether DC might also trigger the innate, NK cell-mediated anti-tumor immunity. In mice with MHC class I-negative tumors, adoptively transferred- or Flt3 ligand-expanded DC promoted NK cell-dependent anti-tumor effects. In vitro studies demonstrated a cell-to-cell contact between DC and resting NK cells that resulted in a substantial increase in both NK cell cytolytic activity and IFN-gamma production. Thus, DC are involved in the interaction between innate and adaptive immune responses.
引用
收藏
页码:405 / 411
页数:7
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