Dynamics of immune cell recruitment during West Nile encephalitis and identification of a new CD19+B220-BST-2+ leukocyte population

被引:48
作者
Brehin, Anne-Claire [1 ,2 ]
Mouries, Juliette [3 ,5 ]
Frenkiel, Marie-Pascale [2 ]
Dadaglio, Gilles [3 ,5 ]
Despres, Philippe [2 ]
Lafon, Monique [1 ]
Couderc, Therese [1 ,4 ]
机构
[1] Inst Pasteur, Neuroimmunol Virale, Paris, France
[2] Inst Pasteur, Unite Interact Mol Flavivirus Hotes, Paris, France
[3] Inst Pasteur, Unite Regulat Immunitaire & Vaccinol, Paris, France
[4] Inst Pasteur, Dept Biol Cellulaire & Infect, Paris, France
[5] Inst Natl Sante & Rech Med, U883, Paris, France
关键词
D O I
10.4049/jimmunol.180.10.6760
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
West Nile virus (WNV) is an emerging neurotropic flavivirus. We investigated the dynamics of immune cell recruitment in peripheral tissues and in the CNS during WNV encephalitis in an immunocompetent mouse model. In the periphery, immune cell expansion can successfully limit viremia and lymphoid tissue infection. However, viral clearance in the periphery is too late to prevent viral invasion of the CNS. In the CNS, innate immune cells, including microglia/macrophages, NK cells, and plasmacytoid dendritic cells, greatly expand as the virus invades the brain, whereas B and T cells are recruited after viral invasion, and fail to control the spread of the virus. Thus, the onset of WNV encephalitis was correlated both with CNS viral infection and with a large local increase of innate immune cells. Interestingly, we identify a new immune cell type: CD19(+)B220(-) BST-2(+), which we name G8-ICs. These cells appear during peripheral infection and enter the CNS. G8-ICs express high levels of MHC class II, stain for viral Ag, and are localized in the paracortical zone of lymph nodes, strongly suggesting they are previously unidentified APCs that appear in response to viral infection.
引用
收藏
页码:6760 / 6767
页数:8
相关论文
共 41 条
[31]   Developmental plasticity of CNS microglia [J].
Santambrogio, L ;
Belyanskaya, SL ;
Fischer, FR ;
Cipriani, B ;
Brosnan, CF ;
Ricciardi-Castagnoli, P ;
Stern, LJ ;
Strominger, JL ;
Riese, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (11) :6295-6300
[32]   Intracerebral recruitment and maturation of dendritic cells in the onset and progression of experimental autoimmune encephalomyelitis [J].
Serafini, B ;
Columba-Cabezas, S ;
Di Rosa, F ;
Aloisi, F .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (06) :1991-2002
[33]   CD8+ T cells require perforin to clear West Nile virus from infected neurons [J].
Shrestha, B ;
Samuel, MA ;
Diamond, MS .
JOURNAL OF VIROLOGY, 2006, 80 (01) :119-129
[34]  
Shrestha B, 2004, J VIROL, V78, P8312, DOI [10.1128/JVI.78.15.8312-8321.2004, 10.1128/jvi.78.15.8312-8321.2004]
[35]   Gamma interferon plays a crucial early antiviral role in protection against West Nile virus infection [J].
Shrestha, Bimmi ;
Wang, Tian ;
Samuel, Melanie A. ;
Whitby, Kevin ;
Craft, Joe ;
Fikrig, Erol ;
Diamond, Michael S. .
JOURNAL OF VIROLOGY, 2006, 80 (11) :5338-5348
[36]   CD4+ T-cell responses are required for clearance of West Nile virus from the central nervous system [J].
Sitati, Elizabeth M. ;
Diamond, Michael S. .
JOURNAL OF VIROLOGY, 2006, 80 (24) :12060-12069
[37]   The use of flow cytometry to evaluate temporal changes in inflammatory cells following focal cerebral ischemia in mice [J].
Stevens, SL ;
Bao, JZ ;
Hollis, J ;
Lessov, NS ;
Clark, WM ;
Stenzel-Poore, MP .
BRAIN RESEARCH, 2002, 932 (1-2) :110-119
[38]   Toll-like receptor 3 mediates West Nile virus entry into the brain causing lethal encephalitis [J].
Wang, T ;
Town, T ;
Alexopoulou, L ;
Anderson, JF ;
Fikrig, E ;
Flavell, RA .
NATURE MEDICINE, 2004, 10 (12) :1366-1373
[39]   CD8+ T cells mediate recovery and immunopathology in west nile virus encephalitis [J].
Wang, Y ;
Lobigs, M ;
Lee, E ;
Müllbacher, A .
JOURNAL OF VIROLOGY, 2003, 77 (24) :13323-13334
[40]  
Wojtera M, 2005, FOLIA NEUROPATHOL, V43, P311