Pluripotent Stem Cells in Clinical Cell Transplantation: Focusing on Induced Pluripotent Stem Cell-Derived RPE Cell Therapy in Age-Related Macular Degeneration

被引:11
作者
Yang, Yi-Ping [1 ,2 ,3 ]
Hsiao, Yu-Jer [1 ,3 ]
Chang, Kao-Jung [1 ,3 ,4 ]
Foustine, Shania [2 ]
Ko, Yu-Ling [1 ]
Tsai, Yi-Ching [1 ]
Tai, Hsiao-Yun [1 ]
Ko, Yu-Chieh [5 ]
Chiou, Shih-Hwa [1 ,2 ,3 ,5 ,6 ]
Lin, Tai-Chi [3 ,5 ]
Chen, Shih-Jen [5 ]
Chien, Yueh [1 ,2 ,3 ]
Hwang, De-Kuang [3 ,4 ,5 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med Res, Taipei 112201, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Coll Med, Inst Pharmacol, Taipei 112304, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Sch Med, Taipei 112304, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Inst Clin Med, Taipei 112304, Taiwan
[5] Taipei Vet Gen Hosp, Dept Ophthalmol, Taipei 112201, Taiwan
[6] Acad Sinica, Genom Res Ctr, Taipei 115201, Taiwan
关键词
pluripotent stem cells; embryonic stem cells; induced pluripotent stem cell; clinical trials; retinal pigment epithelial cells; age-related macular degeneration; cell transplantation; RETINAL-PIGMENT EPITHELIUM; MODELS; MONKEY; MOUSE;
D O I
10.3390/ijms232213794
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human pluripotent stem cells (PSCs), including both embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), represent valuable cell sources to replace diseased or injured tissues in regenerative medicine. iPSCs exhibit the potential for indefinite self-renewal and differentiation into various cell types and can be reprogrammed from somatic tissue that can be easily obtained, paving the way for cell therapy, regenerative medicine, and personalized medicine. Cell therapies using various iPSC-derived cell types are now evolving rapidly for the treatment of clinical diseases, including Parkinson's disease, hematological diseases, cardiomyopathy, osteoarthritis, and retinal diseases. Since the first interventional clinical trial with autologous iPSC-derived retinal pigment epithelial cells (RPEs) for the treatment of age-related macular degeneration (AMD) was accomplished in Japan, several preclinical trials using iPSC suspensions or monolayers have been launched, or are ongoing or completed. The evolution and generation of human leukocyte antigen (HLA)-universal iPSCs may facilitate the clinical application of iPSC-based therapies. Thus, iPSCs hold great promise in the treatment of multiple retinal diseases. The efficacy and adverse effects of iPSC-based retinal therapies should be carefully assessed in ongoing and further clinical trials.
引用
收藏
页数:13
相关论文
共 61 条
[51]   Evaluation of Transplanted Autologous Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium in Exudative Age-Related Macular Degeneration [J].
Takagi, Seiji ;
Mandai, Michiko ;
Gocho, Kiyoko ;
Hirami, Yasuhiko ;
Yamamoto, Midori ;
Fujihara, Masashi ;
Sugita, Sunao ;
Kurimoto, Yasuo ;
Takahashi, Masayo .
OPHTHALMOLOGY RETINA, 2019, 3 (10) :850-859
[52]  
Takahashi Jun, 2020, Regen Ther, V13, P18, DOI 10.1016/j.reth.2020.06.002
[53]   Induction of pluripotent stem cells from adult human fibroblasts by defined factors [J].
Takahashi, Kazutoshi ;
Tanabe, Koji ;
Ohnuki, Mari ;
Narita, Megumi ;
Ichisaka, Tomoko ;
Tomoda, Kiichiro ;
Yamanaka, Shinya .
CELL, 2007, 131 (05) :861-872
[54]   Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors [J].
Takahashi, Kazutoshi ;
Yamanaka, Shinya .
CELL, 2006, 126 (04) :663-676
[55]   DICER1 Loss and Alu RNA Induce Age-Related Macular Degeneration via the NLRP3 Inflammasome and MyD88 [J].
Tarallo, Valeria ;
Hirano, Yoshio ;
Gelfand, Bradley D. ;
Dridi, Sami ;
Kerur, Nagaraj ;
Kim, Younghee ;
Cho, Won Gil ;
Kaneko, Hiroki ;
Fowler, Benjamin J. ;
Bogdanovich, Sasha ;
Albuquerque, Romulo J. C. ;
Hauswirth, William W. ;
Chiodo, Vince A. ;
Kugel, Jennifer F. ;
Goodrich, James A. ;
Ponicsan, Steven L. ;
Chaudhuri, Gautam ;
Murphy, Michael P. ;
Dunaief, Joshua L. ;
Ambati, Balamurali K. ;
Ogura, Yuichiro ;
Yoo, Jae Wook ;
Lee, Dong-ki ;
Provost, Patrick ;
Hinton, David R. ;
Nunez, Gabriel ;
Baffi, Judit Z. ;
Kleinman, Mark E. ;
Ambati, Jayakrishna .
CELL, 2012, 149 (04) :847-859
[56]   Transgenic Mice Expressing Variants of Complement Factor H Develop AMD-like Retinal Findings [J].
Ufret-Vincenty, Rafael L. ;
Aredo, Bogale ;
Liu, Xinran ;
McMahon, Anne ;
Chen, Peter W. ;
Sun, Hui ;
Niederkorn, Jerry Y. ;
Kedzierski, Wojciech .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (11) :5878-5887
[57]   Transplanted neurons integrate into adult retinas and respond to light [J].
Venugopalan, Praseeda ;
Wang, Yan ;
Tu Nguyen ;
Huang, Abigail ;
Muller, Kenneth J. ;
Goldberg, Jeffrey L. .
NATURE COMMUNICATIONS, 2016, 7
[58]   Antioxidant properties of melanin in retinal pigment epithelial cells [J].
Wang, Z ;
Dillon, J ;
Gaillard, ER .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 2006, 82 (02) :474-479
[59]   Transplanted Mouse Embryonic Stem Cell-Derived Retinal Ganglion Cells Integrate and Form Synapses in a Retinal Ganglion Cell-Depleted Mouse Model [J].
Wu, You-Ren ;
Hashiguchi, Tomoyo ;
Sho, Junki ;
Chiou, Shih-Hwa ;
Takahashi, Masayo ;
Mandai, Michiko .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (13)
[60]   An electroactive hybrid biointerface for enhancing neuronal differentiation and axonal outgrowth on bio-subretinal chip [J].
Yang, Jia-Wei ;
Chen, Chong-You ;
Yu, Zih-Yu ;
Chung, Johnson H. Y. ;
Liu, Xiao ;
Wu, Chung-Yu ;
Chen, Guan-Yu .
MATERIALS TODAY BIO, 2022, 14