NKT Cell-Plasmacytoid Dendritic Cell Cooperation via OX40 Controls Viral Infection in a Tissue-Specific Manner

被引:96
作者
Diana, Julien [1 ,2 ]
Griseri, Thibault [1 ,2 ]
Lagaye, Sylvie [1 ,2 ]
Beaudoin, Lucie [1 ,2 ]
Autrusseau, Elodie [1 ,2 ]
Gautron, Anne-Sophie [1 ,2 ]
Tomkiewicz, Celine [2 ,3 ]
Herbelin, Andre [2 ,6 ]
Barouki, Robert [2 ,3 ]
von Herrath, Matthias [5 ]
Dalod, Marc [4 ,7 ,8 ]
Lehuen, Agnes [1 ,2 ]
机构
[1] Hop Cochin St Vincent Paul, INSERM, U561, F-75014 Paris, France
[2] Univ Paris 05, F-75014 Paris, France
[3] INSERM, U747, F-75007 Paris, France
[4] CNRS, UMR6102, F-13288 Marseille, France
[5] La Jolla Inst Allergy & Immunol, San Diego, CA 92037 USA
[6] CNRS, UMR 8147, F-75015 Paris, France
[7] INSERM, U631, F-13288 Marseille, France
[8] Univ Mediterranee, CIML, F-13288 Marseille, France
关键词
KILLER T-CELLS; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; DEPENDENT DIABETES-MELLITUS; NATURAL-KILLER; IMMUNE-RESPONSE; ACTIVATION; MICE; LIGAND; TYPE-1; BETA;
D O I
10.1016/j.immuni.2008.12.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Invariant natural killer T (iNKT) cells promote immune responses to various pathogens, but exactly how iNKT cells control antiviral responses is unclear. Here, we showed that iNKT cells induced tissue-specific antiviral effects in mice infected by lymphocytic choriomeningitis virus (LCMV). Indeed, iNKT cells inhibited viral replication in the pancreas and liver but not in the spleen. In the pancreas, iNKT cells expressed the OX40 molecule and promoted type I interferon (IFN) production by plasmacytoid dendritic cells (pDCs) through OX40-OX40 ligand interaction. Subsequently, this iNKT cell-pDC cooperation attenuated the antiviral adaptive immune response in the pancreas but not in the spleen. The dampening of pancreatic anti-LCMV CD8(+) T cell response prevented tissue damage in transgenic mice expressing LCMV protein in islet beta cells. Thus, this study identifies pDCs as an essential partner of iNKT cells for mounting an efficient, nondeleterious antiviral response in peripheral tissue.
引用
收藏
页码:289 / 299
页数:11
相关论文
共 56 条
[1]   Interleukin-15 and natural killer and NKT cells play a critical role in innate protection against genital herpes simplex virus type 2 infection [J].
Ashkar, AA ;
Rosenthal, KL .
JOURNAL OF VIROLOGY, 2003, 77 (18) :10168-10171
[2]   Mouse strain differences in plasmacytoid dendritic cell frequency and function revealed by a novel monoclonal antibody [J].
Asselin-Paturel, C ;
Brizard, G ;
Pin, JJ ;
Brière, F ;
Trinchieri, G .
JOURNAL OF IMMUNOLOGY, 2003, 171 (12) :6466-6477
[3]   Plasmacytoid dendritic cells - In search of their niche in immune responses [J].
Barchet, W ;
Blasius, A ;
Cella, M ;
Colonna, M .
IMMUNOLOGIC RESEARCH, 2005, 32 (1-3) :75-83
[4]   NKT cells inhibit the onset of diabetes by impairing the development of pathogenic T cells specific for pancreatic β cells [J].
Beaudoin, L ;
Laloux, V ;
Novak, J ;
Lucas, B ;
Lehuen, A .
IMMUNITY, 2002, 17 (06) :725-736
[5]   The biology of NKT cells [J].
Bendelac, Albert ;
Savage, Paul B. ;
Teyton, Luc .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :297-336
[6]   Interferons α and β as immune regulators -: A new look [J].
Biron, CA .
IMMUNITY, 2001, 14 (06) :661-664
[7]   Mechanism of CD1d-restricted natural killer T cell activation during microbial infection [J].
Brigl, M ;
Bry, L ;
Kent, SC ;
Gumperz, JE ;
Brenner, MB .
NATURE IMMUNOLOGY, 2003, 4 (12) :1230-1237
[8]   CD1: Antigen presentation and T cell function [J].
Brigl, M ;
Brenner, MB .
ANNUAL REVIEW OF IMMUNOLOGY, 2004, 22 :817-890
[9]   Activated NKT cells inhibit autoimmune diabetes through tolerogenic recruitment of dendritic cells to pancreatic lymph nodes [J].
Chen, YG ;
Choisy-Rossi, CM ;
Holl, TM ;
Chapman, HD ;
Besra, GS ;
Porcelli, SA ;
Shaffer, DJ ;
Roopenian, D ;
Wilson, SB ;
Serreze, DV .
JOURNAL OF IMMUNOLOGY, 2005, 174 (03) :1196-1204
[10]   OX40 (CD 134) blockade inhibits the co-stimulatory cascade and promotes heart allograft survival [J].
Curry, AJ ;
Chikwe, J ;
Smith, XG ;
Cai, M ;
Schwarz, H ;
Bradley, JA ;
Bolton, EM .
TRANSPLANTATION, 2004, 78 (06) :807-814