Current Challenges of iPSC-Based Disease Modeling and Therapeutic Implications

被引:319
作者
Doss, Michael Xavier [1 ]
Sachinidis, Agapios [2 ,3 ]
机构
[1] BioMarin Pharmaceut Inc, Technol Dev Div, 105 Digital Dr, Novato, CA 94949 USA
[2] Univ Cologne, Inst Neurophysiol, Robert Koch Str 39, D-50931 Cologne, Germany
[3] Univ Cologne, Ctr Mol Med, Robert Koch Str 39, D-50931 Cologne, Germany
关键词
induced pluripotent stem cells; cell replacement therapy; drug discovery; safety pharmacology; disease modeling; autologous cell therapy; allogenic cell therapy; clinical trials with stem cells; PLURIPOTENT STEM-CELLS; EPIGENETIC MEMORY; ENDOTHELIAL-CELLS; GENERATION; CANCER; MOUSE; CARDIOMYOCYTES; EFFICIENT; TOOL; DIFFERENTIATION;
D O I
10.3390/cells8050403
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Induced pluripotent stem cell (iPSC)-based disease modelling and the cell replacement therapy approach have proven to be very powerful and instrumental in biomedical research and personalized regenerative medicine as evidenced in the past decade by unraveling novel pathological mechanisms of a multitude of monogenic diseases at the cellular level and the ongoing and emerging clinical trials with iPSC-derived cell products. iPSC-based disease modelling has sparked widespread enthusiasm and has presented an unprecedented opportunity in high throughput drug discovery platforms and safety pharmacology in association with three-dimensional multicellular organoids such as personalized organs-on-chips, gene/base editing, artificial intelligence and high throughput omics methodologies. This critical review summarizes the progress made in the past decade with the advent of iPSC discovery in biomedical applications and regenerative medicine with case examples and the current major challenges that need to be addressed to unleash the full potential of iPSCs in clinical settings and pharmacology for more effective and safer regenerative therapy.
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页数:16
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