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Large-scale generation of IL-12 secreting macrophages from human pluripotent stem cells for cancer therapy.
Kang, Baoqiang; Xing, Qi; Huang, Yuhua; Lin, Huaisong; Peng, Jiaojiao; Zhang, Zhishuai; Wang, Mingquan; Guo, Xinrui; Hu, Xing; Wang, Shuoting; Wang, Junwei; Gao, Minghui; Zhu, Yanling; Pan, Guangjin.
Afiliación
  • Kang B; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Xing Q; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Huang Y; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Lin H; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Peng J; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Zhang Z; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Wang M; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Guo X; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Hu X; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Wang S; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Wang J; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
  • Gao M; Key Lab for Rare & Uncommon Diseases of Shandong Province, Biomedical Sciences College & Shandong Medicinal Biotechnology Centre, Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan 250117, Shandong, China.
  • Zhu Y; Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan 250117, Shandong, China.
  • Pan G; CAS Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Hong Kong; Center for Cellular and Biotherapy, Guangzhou Institutes of Biomedicine and H
Mol Ther Methods Clin Dev ; 32(1): 101204, 2024 Mar 14.
Article en En | MEDLINE | ID: mdl-38390556
ABSTRACT
Genetically engineered macrophages (GEMs) have emerged as an appealing strategy to treat cancers, but they are largely impeded by the cell availability and technical challenges in gene transfer. Here, we develop an efficient approach to generate large-scale macrophages from human induced pluripotent stem cells (hiPSCs). Starting with 1 T150 dish of 106 hiPSCs, more than 109 mature macrophages (iMacs) could be generated within 1 month. The generated iMacs exhibit typical macrophage properties such as phagocytosis and polarization. We then generate hiPSCs integrated with an IL-12 expression cassette in the AAVS1 locus to produce iMacs secreting IL-12, a strong proimmunity cytokine. hiPSC-derived iMacs_IL-12 prevent cytotoxic T cell exhaustion and activate T cells to kill different cancer cells. Furthermore, iMacs_IL-12 display strong antitumor effects in a T cell-dependent manner in subcutaneously or systemically xenografted mice of human lung cancer. Therefore, we provide an off-the-shelf strategy to produce large-scale GEMs for cancer therapy.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Mol Ther Methods Clin Dev Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Mol Ther Methods Clin Dev Año: 2024 Tipo del documento: Article