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タイトル
  • en Tumor-infiltrating DCs suppress nucleic acid-mediated innate immune responses through interactions between the receptor TIM-3 and the alarmin HMGB1
作成者
    • en Chiba, Shigeki
    • en Baghdadi, Muhammad
    • en Akiba, Hisaya
    • en Dosaka-Akita, Hirotoshi
    • en Fujioka, Yoichiro
    • en Gorman, Jacob V.
    • en Colgan, John D.
    • en Hirashima, Mitsuomi
    • en Yagita, Hideo
    • en Jinushi, Masahisa
アクセス権 open access
主題
  • Other en TIM-3
  • Other en HMGB1
  • Other en Nucleic acids
  • Other en Innate immunity
  • Other en Dendritic cells
  • NDC 493
内容注記
  • Abstract en The mechanisms by which tumor microenvironments modulate nucleic acid-mediated innate immunity remain unknown. Here, we identified the receptor TIM-3 as key to circumventing the stimulatory effects of nucleic acids in tumor immunity. TIM-3 is highly expressed on tumor-associated dendritic cells (DC) in murine tumors and cancer patients. DC-derived TIM-3 suppresses innate immune responses through Toll-like receptor and cytosolic sensor recognition of nucleic acids via a galectin-9 independent mechanism. Instead, TIM-3 interacts with the HMGB1 to interfere with recruitment of nucleic acids into DC endosomes and attenuates the therapeutic efficacy of DNA vaccination and chemotherapy by reducing immunogenicity of nucleic acids released from dying tumor cells. Together, these findings define a novel mechanism by which tumor microenvironments suppress antitumor immunity mediated by nucleic acids.
出版者 en Nature Publishing Group
日付
    Issued2012-09
言語
  • eng
資源タイプ journal article
出版タイプ AM
資源識別子 HDL http://hdl.handle.net/2115/52108
関連
  • isVersionOf DOI https://doi.org/10.1038/ni.2376
収録誌情報
    • PISSN 1529-2908
      • en Nature Immunology
      • 13 9 開始ページ832 終了ページ842
ファイル
コンテンツ更新日時 2023-07-26