Temporal changes in dendritic cell subsets, cross-priming and costimulation via CD70 control CD8+ T cell responses to influenza

被引:217
|
作者
Ballesteros-Tato, Andre [1 ]
Leon, Beatriz [1 ]
Lund, Frances E. [1 ]
Randall, Troy D. [1 ]
机构
[1] Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA
基金
美国国家卫生研究院;
关键词
IN-VIVO; LYMPH-NODE; ANTIGEN PRESENTATION; ADAPTIVE IMMUNITY; EPITHELIAL-CELLS; LIGAND CD70; VIRUS; INDUCTION; ACTIVATION; INFECTION;
D O I
10.1038/ni.1838
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The question of which dendritic cells (DCs) respond to pulmonary antigens and cross-prime CD8(+) T cells remains controversial. We show here that influenza-specific CD8(+) T cell priming was controlled by different DCs at different times after infection. Whereas early priming was controlled by both CD103(+)CD11b(lo) and CD103-CD11b(hi) DCs, CD103-CD11b(hi) DCs dominated antigen presentation at the peak of infection. Moreover, CD103-CD11b(hi) DCs captured exogenous antigens in the lungs and directly cross-primed CD8(+) T cells in the draining lymph nodes without transferring antigen to CD8(alpha)(+) DCs. Finally, we show that CD103-CD11b(hi) DCs were the only DCs to express CD70 after influenza infection and that CD70 expression on CD103-CD11b(hi) DCs licensed them to expand CD8(+) T cell populations responding to both influenza and exogenous ovalbumin.
引用
收藏
页码:216 / U4
页数:10
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