RRC ID 44418
著者 Shimizu K, Asakura M, Shinga J, Sato Y, Kitahara S, Hoshino K, Kaisho T, Schoenberger SP, Ezaki T, Fujii S.
タイトル Invariant NKT cells induce plasmacytoid dendritic cell (DC) cross-talk with conventional DCs for efficient memory CD8+ T cell induction.
ジャーナル J Immunol
Abstract A key goal of vaccine immunotherapy is the generation of long-term memory CD8(+) T cells capable of mediating immune surveillance. We discovered a novel intercellular pathway governing the development of potent memory CD8(+) T cell responses against cell-associated Ags that is mediated through cross-presentation by XCR1(+) dendritic cells (DCs). Generation of CD8(+) memory T cells against tumor cells pulsed with an invariant NKT cell ligand depended on cross-talk between XCR1(+) and plasmacytoid DCs that was regulated by IFN-α/IFN-αR signals. IFN-α production by plasmacytoid DCs was stimulated by an OX40 signal from the invariant NKT cells, as well as an HMGB1 signal from the dying tumor cells. These findings reveal a previously unknown pathway of intercellular collaboration for the generation of tumor-specific CD8(+) memory T cells that can be exploited for strategic vaccination in the setting of tumor immunotherapy.
巻・号 190(11)
ページ 5609-19
公開日 2013-6-1
DOI 10.4049/jimmunol.1300033
PII jimmunol.1300033
PMID 23630347
MeSH Animals CD8-Positive T-Lymphocytes / immunology* Cell Communication / immunology* Cell Line, Tumor Chemotaxis / immunology Dendritic Cells / immunology* Dendritic Cells / metabolism Immunologic Memory* Interferon Type I / immunology Interferon Type I / metabolism Interleukin-12 / biosynthesis Ligands Mice Natural Killer T-Cells / immunology* Neoplasms / immunology Signal Transduction
IF 4.886
引用数 24
WOS 分野 IMMUNOLOGY
リソース情報
ヒト・動物細胞