Influenza Virus and Poly(I:C) Inhibit MHC Class I-Restricted Presentation of Cell-Associated Antigens Derived from Infected Dead Cells Captured by Human Dendritic Cells

被引:15
|
作者
Frleta, Davor
Yu, Chun I.
Klechevsky, Eynav
Flamar, Anne-Laure
Zurawski, Gerard
Banchereau, Jacques
Palucka, A. Karolina [1 ]
机构
[1] Baylor Inst Immunol Res, Baylor Natl Inst Allergy & Infect Dis, Cooperat Ctr Translat Res Human Immunol & Biodef, Dallas, TX 75204 USA
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 182卷 / 05期
关键词
TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; CD8(+) T-CELLS; PHAGOSOME MATURATION; CROSS-PRESENTATION; CTL; RECOGNITION; INDUCTION; TOLERANCE; RESPONSES;
D O I
10.4049/jimmunol.0801720
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During viral infection, dendritic cells (DCs) capture infected cells and present viral Ags to CD8(+) T cells. However, activated DCs might potentially present cell-associated Ags derived from captured dead cells. In this study, we find that human DCs that captured dead cells containing the TLR3 agonist poly(I:C) produced cytokines and underwent maturation, but failed to elicit autologous CD8(+) T cell responses against Ags of dead cells. Accordingly, DCs that captured dead cells containing poly(I:C), or influenza virus, are unable to activate CD8(+) T cell clones specific to cell-associated Ags of captured dead cells. CD4(+) T cells are expanded with DCs that have captured poly (I:C)-containing dead cells, indicating the inhibition is specific for MHC class I-restricted cross-presentation. Furthermore, these DCs can expand naive allogeneic CD8(+) T cells. Finally, soluble or targeted Ag is presented when coloaded onto DCs that have captured poly(I:C)-containing dead cells, indicating the inhibition is specific for dead cell cargo that is accompanied by viral or poly(I:C) stimulus. Thus, DCs have a mechanism that prevents MHC class I-restricted cross-presentation of cell-associated Ag when they have captured dead infected cells. The Journal of Immunology, 2009, 182: 2766-2776.
引用
收藏
页码:2766 / 2776
页数:11
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