Large-scale generation of IL-12 secreting macrophages from human pluripotent stem cells for cancer therapy

被引:2
|
作者
Kang, Baoqiang [1 ]
Xing, Qi [1 ,2 ]
Huang, Yuhua [1 ,2 ]
Lin, Huaisong [1 ]
Peng, Jiaojiao [1 ,2 ,8 ]
Zhang, Zhishuai [1 ,2 ]
Wang, Mingquan [1 ,8 ]
Guo, Xinrui [3 ,4 ,5 ]
Hu, Xing [1 ,2 ]
Wang, Shuoting [6 ,7 ]
Wang, Junwei [7 ]
Gao, Minghui [7 ]
Zhu, Yanling [1 ,2 ]
Pan, Guangjin [1 ,2 ,3 ]
机构
[1] Hong Kong Inst Sci & Innovat, Ctr Regenerat Med & Hlth, CAS Key Lab Regenerat Biol, Guangdong Prov Key Lab Stem Cell & Regenerat Med, Hong Kong, Peoples R China
[2] Chinese Acad Sci, Ctr Cellular & Biotherapy, Guangzhou Inst Biomed & Hlth, Guangzhou 510530, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Shandong First Med & Univ Shandong Acad Med Sci, Biomed Sci Coll, Key Lab Rare & Uncommon Dis Shandong Prov, Jinan 250117, Shandong, Peoples R China
[5] Shandong First Med & Univ Shandong Acad Med Sci, Shandong Med Biotechnol Ctr, Jinan 250117, Shandong, Peoples R China
[6] Shandong First Med Univ & Shandong Acad Med Sci, Jinan 250117, Shandong, Peoples R China
[7] Sun Yat Sen Univ, Affiliated Hosp 3, Guangzhou 510630, Peoples R China
[8] Chinese Acad Sci, Anal & Testing Ctr Guangzhou Inst Biomed & Hlth, Guangzhou 510530, Peoples R China
基金
中国国家自然科学基金;
关键词
TUMOR-ASSOCIATED MACROPHAGES; T-CELLS; INTERLEUKIN-12; RESISTANCE; PLATFORM; INNATE;
D O I
10.1016/j.omtm.2024.101204
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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. 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 systemicallyxenografted mice of human lung cancer. Therefore, we provide an off-the-shelf strategy to produce large-scale GEMs for cancer therapy.
引用
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页数:13
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