Immunogenicity and functional evaluation of iPSC-derived organs for transplantation

被引:26
作者
Wang, Libin [1 ,2 ]
Cao, Jiani [1 ]
Wang, Yukai [1 ]
Lan, Tianshu [3 ]
Liu, Lei [1 ]
Wang, Weixu [1 ]
Jin, Ning [3 ]
Gong, Jiaqi [1 ]
Zhang, Chao [1 ]
Teng, Fei [1 ]
Yan, Guoliang [3 ]
Li, Chun [3 ]
Li, Jiali [3 ]
Wan, Haifeng [1 ]
Hu, Baoyang [1 ]
Li, Wei [1 ]
Zhao, Xiaoyang [1 ]
Qi, Zhongquan [3 ]
Zhao, Tongbiao [1 ]
Zhou, Qi [1 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Reprod Biol, Beijing, Peoples R China
[2] Grad Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Xiamen Univ, Organ Transplantat Inst, Xiamen, Peoples R China
基金
中国国家自然科学基金;
关键词
iPSC-derived organs; immunogenicity; transplantation; PLURIPOTENT STEM-CELLS; DOPAMINE NEURONS; ES CELLS; MOUSE; GENERATION; TUMORIGENICITY; MICE; FIBROBLASTS; MODELS;
D O I
10.1038/celldisc.2015.15
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Whether physiologically induced pluripotent stem cell (iPSC)-derived organs are immunogenic and can be used for transplantation is unclear. Here, we generated iPSC-derived skin, islet, and heart representing three germ layers of the body through 4n complementation and evaluated their immunogenicity and therapeutic efficacy. Upon transplantation into recipient mice, iPSC-derived skin successfully survived and repaired local tissue wounds. In diabetic mouse models, explanted iPSC-derived islets effectively produced insulin and lowered blood glucose to basal levels. iPSC-derived heart grafts maintained normal beating for more than 3 months in syngeneic recipients. Importantly, no obvious immune rejection responses against iPSC-derived organs were detected long after transplantation. Our study not only demonstrates the fundamental immunogenicity and function of iPSC derivatives, but also provides preclinical evidence to support the feasibility of using iPSC-derived skin, islet, and heart for therapeutic use.
引用
收藏
页数:11
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