Dendritic cells at a DNA vaccination site express the encoded influenza nucleoprotein and prime MHC class I-restricted cytolytic lymphocytes upon adoptive transfer
被引:30
作者:
Bot, A
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机构:Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
Bot, A
Stan, AC
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机构:Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
Stan, AC
Inaba, K
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机构:Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
Inaba, K
Steinman, R
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机构:Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
Steinman, R
Bona, C
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机构:Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
Bona, C
机构:
[1] Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
[2] Kyoto Univ, Immunol Lab, Dept Zool, Kyoto 606, Japan
[3] Rockefeller Univ, Lab Cell Biol & Immunol, New York, NY 10021 USA
adoptive transfer;
cytotoxic cells;
dendritic cells;
DNA vaccination;
nucleoprotein;
D O I:
10.1093/intimm/12.6.825
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Intradermal inoculation of plasmids expressing antigens that contain MHC class I-restricted epitopes leads to the induction of specific CD8(+) cytotoxic T lymphocytes (CTL). The role of in situ transfected antigen-presenting cells (APC) in the priming of specific CTL subsequent to intradermal DNA immunization was investigated using a plasmid (NPV1) expressing the nucleoprotein (NP) of influenza virus that contains a nuclear targeting signal and a dominant class I/K-d-restricted epitope. Inoculation of NPV1 leads to in situ transfection of MHC class II+ and class II- cells, as revealed by the nuclear localization of NP. Between 2 and 3% of MHC class II+ and class II- cells with the ability to migrate out of the epidermis expressed NP. Upon adoptive transfer into naive recipients, class II+ migratory cells recovered from the area inoculated with NP-expressing plasmid were significantly superior regarding the ability to prime virus-specific CTL as compared to MHC class II- cells. Together, these results are consistent with the role of local dendritic cells loaded with antigen in the priming of CTL by intradermal DNA immunization.