Intramuscular and intracutaneous immunization with naked DNA can vaccinate animals to the encoded proteins, but the underlying mechanisms of antigen presentation are unclear. We used DNA that encodes an A/PR/8/34 influenza peptide for CD4 T cells and that elicits protective antiviral immunity. DNA-transfected, cultured muscle cells released the influenza polypeptide, which then could be presented on the major histocompatibility complex class II molecules of dendritic cells. When DNA was injected into muscles or skin, and antigen-presenting cells were isolated from either the draining lymph nodes or the skin, dendritic, but not B, cells presented antigen to T cells and carried plasmid DNA. We suggest that the uptake of DNA and/or the protein expressed by dendritic cells triggers immune responses to DNA vaccines.
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3 November 1997
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November 03 1997
Antigen Presentation by Dendritic Cells after Immunization with DNA Encoding a Major Histocompatibility Complex Class II–restricted Viral Epitope
Sofia Casares,
Sofia Casares
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
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Kayo Inaba,
Kayo Inaba
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
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Teodor-Doru Brumeanu,
Teodor-Doru Brumeanu
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
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Ralph M. Steinman,
Ralph M. Steinman
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
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Constantin A. Bona
Constantin A. Bona
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
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Sofia Casares
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
Kayo Inaba
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
Teodor-Doru Brumeanu
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
Ralph M. Steinman
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
Constantin A. Bona
From the *Department of Microbiology, Mount Sinai School of Medicine, New York 10029; the ‡Laboratory of Immunology, Department of Zoology, Faculty of Science, Kyoto University, Japan; and the §Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York 10021
Address correspondence to C.A. Bona, Department of Microbiology, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, Box 1124, New York, NY 10029. Phone: 212-241-6924; FAX: 212-423-0711; E-mail: [email protected]
1
Abbreviations used in this paper: HA, hemagglutinin; pC, plasmid control; TcH, T cell hybridoma.
Received:
June 26 1997
Revision Received:
August 20 1997
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1997
J Exp Med (1997) 186 (9): 1481–1486.
Article history
Received:
June 26 1997
Revision Received:
August 20 1997
Citation
Sofia Casares, Kayo Inaba, Teodor-Doru Brumeanu, Ralph M. Steinman, Constantin A. Bona; Antigen Presentation by Dendritic Cells after Immunization with DNA Encoding a Major Histocompatibility Complex Class II–restricted Viral Epitope . J Exp Med 3 November 1997; 186 (9): 1481–1486. doi: https://doi.org/10.1084/jem.186.9.1481
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