A novel dendritic cell subset involved in tumor immunosurveillance

被引:322
作者
Taieb, J
Chaput, N
Ménard, C
Apetoh, L
Ullrich, E
Bonmort, M
Péquignot, M
Casares, N
Terme, M
Flament, C
Opolon, P
Lecluse, Y
Métivier, D
Tomasello, E
Vivier, E
Ghiringhelli, F
Martin, F
Klatzmann, D
Poynard, T
Tursz, T
Raposo, G
Yagita, H
Ryffel, B
Kroemer, G
Zitvogel, L [1 ]
机构
[1] Inst Gustave Roussy, Fac Med Kremlin Bicetre, INSERM, ERM0208, Villejuif, France
[2] Inst Gustave Roussy, CNRS, UMR8125, Villejuif, France
[3] Inst Gustave Roussy, IFR54, Flow Cytometry Core Facil, Villejuif, France
[4] Univ Mediterranee, Ctr Immunol Marseille Luminy, CNRS, INSERM, Marseille, France
[5] Fac Med, INSERM, U517, Dijon, France
[6] Grp Hosp Pitie Salpetriere, CERVI, UPMC, CNRS,UMR7087, F-75634 Paris, France
[7] Hop La Pitie Salpetriere, AH HP, Dept Gastroenterol, Paris, France
[8] Inst Curie, CNRS, UMR144, F-75231 Paris, France
[9] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 113, Japan
[10] Inst Transgenose, CNRS, IEM 2815, Orleans, France
关键词
D O I
10.1038/nm1356
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
The interferon (IFN)-gamma-induced TRAIL effector mechanism is a vital component of cancer immunosurveillance by natural killer (NK) cells in mice(1,2). Here we show that the main source of IFN-gamma is not the conventional NK cell but a subset of B220(+)Ly6C(-) dendritic cells, which are atypical insofar as they express NK cell-surface molecules. Upon contact with a variety of tumor cells that are poorly recognized by NK cells, B220(+)NK1.1(+) dendritic cells secrete high levels of IFN-gamma and mediate TRAIL-dependent lysis of tumor cells. Adoptive transfer of these IFN-producing killer dendritic cells (IKDCs) into tumor-bearing Rag2(-/-)Il2rg(-/-) mice prevented tumor outgrowth, whereas transfer of conventional NK cells did not. In conclusion, we identified IKDCs as pivotal sensors and effectors of the innate antitumor immune response.
引用
收藏
页码:214 / 219
页数:6
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