Improved safety of induced pluripotent stem cell-derived antigen-presenting cell-based cancer immunotherapy.

HSV-TK antigen-presenting cell c-Myc cancer immunotherapy granulocyte-macrophage colony-stimulating factor iCasp9 induced pluripotent stem cell suicide gene

Journal

Molecular therapy. Methods & clinical development
ISSN: 2329-0501
Titre abrégé: Mol Ther Methods Clin Dev
Pays: United States
ID NLM: 101624857

Informations de publication

Date de publication:
11 Jun 2021
Historique:
received: 22 09 2020
accepted: 02 03 2021
entrez: 5 4 2021
pubmed: 6 4 2021
medline: 6 4 2021
Statut: epublish

Résumé

The tumorigenicity and toxicity of induced pluripotent stem cells (iPSCs) and their derivatives are major safety concerns in their clinical application. Recently, we developed granulocyte-macrophage colony-stimulating factor (GM-CSF)-producing proliferating myeloid cells (GM-pMCs) from mouse iPSCs as a source of unlimited antigen-presenting cells for use in cancer immunotherapy. As GM-pMCs are generated by introducing

Identifiants

pubmed: 33816647
doi: 10.1016/j.omtm.2021.03.002
pii: S2329-0501(21)00041-3
pmc: PMC7994724
doi:

Types de publication

Journal Article

Langues

eng

Pagination

171-179

Informations de copyright

© 2021 The Author(s).

Déclaration de conflit d'intérêts

Y.U. received research funding from AGC, Inc., Japan. The remaining authors declare no competing interests.

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Auteurs

Hiroaki Mashima (H)

Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.
Department of Gastroenterological and Transplant Surgery, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima 734-8551, Japan.

Rong Zhang (R)

Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.

Tsuyoshi Kobayashi (T)

Department of Gastroenterological and Transplant Surgery, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima 734-8551, Japan.

Hirotake Tsukamoto (H)

Department of Immunology, Faculty of Life Sciences, Kumamoto University, Kumamoto 860-8556, Japan.

Tianyi Liu (T)

Key Laboratory of Cancer Center, Chinese PLA General Hospital, Beijing 100853, China.

Tatsuaki Iwama (T)

Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.

Yuichiro Hagiya (Y)

Biochemistry Team, Bio Science Division, Technology General Division, Materials Integration Laboratories, AGC, Inc., Yokohama 221-8755, Japan.

Masateru Yamamoto (M)

Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.
Department of Gastroenterological and Transplant Surgery, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima 734-8551, Japan.

Satoshi Fukushima (S)

Department of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto 860-8556, Japan.

Seiji Okada (S)

Division of Hematopoiesis, Center for AIDS Research, Kumamoto University, Kumamoto 860-8556, Japan.

Alimjan Idiris (A)

Biochemistry Team, Bio Science Division, Technology General Division, Materials Integration Laboratories, AGC, Inc., Yokohama 221-8755, Japan.

Shin Kaneko (S)

Shin Kaneko Laboratory, Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, 606-8507, Japan.

Tetsuya Nakatsura (T)

Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.

Hideki Ohdan (H)

Department of Gastroenterological and Transplant Surgery, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima 734-8551, Japan.

Yasushi Uemura (Y)

Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.

Classifications MeSH