Cross-presenting CD103+ dendritic cells are protected from influenza virus infection

被引:195
作者
Helft, Julie [1 ,2 ]
Manicassamy, Balaji [3 ,4 ]
Guermonprez, Pierre [5 ,6 ]
Hashimoto, Daigo [1 ,2 ]
Silvin, Aymeric [1 ,2 ]
Agudo, Judith [2 ,7 ]
Brown, Brian D. [2 ,7 ]
Schmolke, Mirco [3 ,4 ]
Miller, Jennifer C. [1 ,2 ]
Leboeuf, Marylene [1 ,2 ]
Murphy, Kenneth M. [8 ,9 ]
Garcia-Sastre, Adolfo [3 ,4 ,10 ]
Merad, Miriam [1 ,2 ,11 ]
机构
[1] Mt Sinai Sch Med, Dept Oncol Sci, New York, NY USA
[2] Mt Sinai Sch Med, Inst Immunol, New York, NY 10029 USA
[3] Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
[4] Mt Sinai Sch Med, Global Hlth & Emerging Pathogens Inst, New York, NY 10029 USA
[5] Kings Coll London, Ctr Mol & Cellular Biol Inflammat, London WC2R 2LS, England
[6] Kings Coll London, Div Immunol Infect & Inflammatory Dis, London WC2R 2LS, England
[7] Mt Sinai Sch Med, Dept Genet & Genom Sci, New York, NY 10029 USA
[8] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[9] Washington Univ, Sch Med, Howard Hughes Med Inst, St Louis, MO 63110 USA
[10] Mt Sinai Sch Med, Dept Med, Div Infect Dis, New York, NY 10029 USA
[11] NIAID, Mucosal Immunol Studies Team, Portland, OR USA
关键词
MHC CLASS-I; ANTIGEN; SUBSETS; RESPONSES; IMMUNITY; INNATE; INTERFERONS; INDUCTION; CAPACITY; DYNAMICS;
D O I
10.1172/JCI60659
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
CD8(+) cytotoxic T cells are critical for viral clearance from the lungs upon influenza virus infection. The contribution of antigen cross-presentation by DCs to the induction of anti-viral cytotoxic T cells remains controversial. Here, we used a recombinant influenza virus expressing a nonstructural 1-GFP (NS1-GFP) reporter gene to visualize the route of antigen presentation by lung DCs upon viral infection in mice. We found that lung CD103(+) DCs were the only subset of cells that carried intact GFP protein to the draining LNs. Strikingly, lung migratory CD103(+) DCs were not productively infected by influenza virus and thus were able to induce virus-specific CD8(+) T cells through the cross-presentation of antigens from virally infected cells. We also observed that CD103(+) DC resistance to infection correlates with an increased anti-viral state in these cells that is dependent on the expression of type I IFN receptor. These results show that efficient cross-priming by migratory lung DCs is coupled to the acquisition of an anti-viral status, which is dependent on the type I IFN signaling pathway.
引用
收藏
页码:4037 / 4047
页数:11
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