共 43 条
Temporal changes in dendritic cell subsets, cross-priming and costimulation via CD70 control CD8+ T cell responses to influenza
被引:217
作者:

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Leon, Beatriz
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Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA

Lund, Frances E.
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h-index: 0
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Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA

Randall, Troy D.
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Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA Univ Rochester, Div Allergy Immunol & Rheumatol, Rochester, NY 14627 USA
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.
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页码:216 / U4
页数:10
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