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Satoshi Fukushima

Kumamoto University - Department of Dermatology and Plastic Surgery

2-39-1 Kurokami, Chuo Ward

Kumamoto, 860-0862

Japan

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Scholarly Papers (1)

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Type I Interferon Delivery by iPSC-Derived Myeloid Cells Elicits Antitumor Immunity Via XCR1 + Dendritic Cells

Number of pages: 100 Posted: 27 Feb 2019
Nobuhiro Tsuchiya, Rong Zhang, Tatsuaki Iwama, Norihiro Ueda, Tianyi Liu, Minako Tatsumi, Yutaka Sasaki, Ranmaru Shimoda, Yuki Osako, Yu Sawada, Yosuke Kubo, Azusa Miyashita, Satoshi Fukushima, Ryo Nakaki, Keiyo Takubo, Seiji Okada, Shin Kaneko, Hironobu Ihn, Tsuneyasu Kaisho, Yasuharu Nishimura, Satoru Senju, Itaru Endo, Tetsuya Nakatsura and Yasushi Uemura
National Cancer Center, Japan - Division of Cancer Immunotherapy, National Cancer Center, Japan - Division of Cancer Immunotherapy, National Cancer Center, Japan - Division of Cancer Immunotherapy, Kyoto University - Shin Kaneko Laboratory, Aichi Cancer Center - Division of Immunology, Aichi Cancer Center - Division of Immunology, Kansai Medical University - Department of Stem Cell Biology and Regenerative Medicine, Rhelixa Inc., Rhelixa Inc., Yokohama City University - Department of Gastroenterological Surgery, Kumamoto University - Department of Dermatology and Plastic Surgery, Kumamoto University - Department of Dermatology and Plastic Surgery, Kumamoto University - Department of Dermatology and Plastic Surgery, Rhelixa Inc., National Center for Global Health and Medicine - Department of Stem Cell Biology, Kumamoto University - Division of Hematopoiesis, Kyoto University - Shin Kaneko Laboratory, Kumamoto University - Department of Dermatology and Plastic Surgery, Wakayama Medical University - Department of Immunology, Kumamoto University - Department of Immunogenetics, Kumamoto University - Department of Immunogenetics, Yokohama City University - Department of Gastroenterological Surgery, National Cancer Center, Japan - Division of Cancer Immunotherapy and National Cancer Center, Japan - Division of Cancer Immunotherapy
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Abstract:

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Cancer immunotherapy, iPS cell, type I interferon, XCR1, dendritic cells, cross-presentation, checkpoint blockade, PD-1, STING, CXCR3