Pluripotent stem cell therapy for retinal diseases

被引:21
作者
Ahmed, Ishrat [1 ]
Johnston, Robert J., Jr. [2 ]
Singh, Mandeep S. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
关键词
Retinitis pigmentosa (RP); age-related macular degeneration (AMD); embryonic stem cell (ESC); induced pluripotent stem cell (iPSC); retinal organoid; PIGMENT EPITHELIUM; MACULAR DEGENERATION; STARGARDT DISEASE; GENE-THERAPY; AUTOLOGOUS TRANSLOCATION; CHOROID TRANSLOCATION; EFFICIENT GENERATION; CLINICAL-TRIALS; VISUAL FUNCTION; TRANSPLANTATION;
D O I
10.21037/atm-20-4747
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pluripotent stem cells (PSCs), which include human embryonic stem cells (hESCs) and induced pluripotent stem cell (iPSC), have been used to study development of disease processes, and as potential therapies in multiple organ systems. In recent years, there has been increasing interest in the use of PSC-based transplantation to treat disorders of the retina in which retinal cells have been functionally damaged or lost through degeneration. The retina, which consists of neuronal tissue, provides an excellent system to test the therapeutic utility of PSC-based transplantation due to its accessibility and the availability of high -resolution imaging technology to evaluate effects. Preclinical trials in animal models of retinal diseases have shown improvement in visual outcomes following subretinal transplantation of PSC-derived photoreceptors or retinal pigment epithelium (RPE) cells. This review focuses on preclinical studies and clinical trials exploring the use of PSCs for retinal diseases. To date, several phase I/II clinical trials in patients with age-related macular degeneration (AMD) and Stargardt disease (STGD1) have demonstrated the safety and feasibility of PSC-derived RPE transplantation. Additional phase I/II clinical trials using PSC-derived RPE or photoreceptor cells for the treatment of AMD, STGD1, and also retinitis pigmentosa (RP) are currently in the pipeline. As this field continues to evolve, additional technologies may enhance PSC-derived cell transplantation through gene-editing of autologous cells, transplantation of more complex cellular structures such as organoids, and monitoring of transplanted cells through novel imaging technologies.
引用
收藏
页数:17
相关论文
共 118 条
[41]   Autologous translocation of the choroid and retinal pigment epithelium in patients with geographic atrophy [J].
Joussen, Antonia M. ;
Joeres, Sandra ;
Fawzy, Nader ;
Heussen, Florian M. A. ;
Llacer, Helene ;
van Meurs, Jan C. ;
Kirchhof, Bernd .
OPHTHALMOLOGY, 2007, 114 (03) :551-560
[42]   Autologous translocation of the choroid and retinal pigment epithelium in age-related macular degeneration. [J].
Joussen, Antonia M. ;
Heussen, Florian M. A. ;
Joeres, Sandra ;
Llacer, Helene ;
Prinz, Beate ;
Rohrschneider, Klaus ;
Maaijwee, Kristel J. M. ;
van Meurs, Jan ;
Kirchhof, Bernd .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 2006, 142 (01) :17-30
[43]   Scaffolds and stem cells: delivery of cell transplants for retinal degenerations [J].
Kador, Karl E. ;
Goldberg, Jeffrey L. .
EXPERT REVIEW OF OPHTHALMOLOGY, 2012, 7 (05) :459-470
[44]   Characterization of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium Cell Sheets Aiming for Clinical Application [J].
Kamao, Hiroyuki ;
Mandai, Michiko ;
Okamoto, Satoshi ;
Sakai, Noriko ;
Suga, Akiko ;
Sugita, Sunao ;
Kiryu, Junichi ;
Takahashi, Masayo .
STEM CELL REPORTS, 2014, 2 (02) :205-218
[45]   A bioengineered retinal pigment epithelial monolayer for advanced, dry age-related macular degeneration [J].
Kashani, Amir H. ;
Lebkowski, Jane S. ;
Rahhal, Firas M. ;
Avery, Robert L. ;
Salehi-Had, Hani ;
Dang, Wei ;
Lin, Chih-Min ;
Mitra, Debbie ;
Zhu, Danhong ;
Thomas, Biju B. ;
Hikita, Sherry T. ;
Pennington, Britney O. ;
Johnson, Lincoln V. ;
Clegg, Dennis O. ;
Hinton, David R. ;
Humayun, Mark S. .
SCIENCE TRANSLATIONAL MEDICINE, 2018, 10 (435)
[46]   Concise Review: Current Status of Three-Dimensional Organoids as Preclinical Models [J].
Kaushik, Garima ;
Ponnusamy, Moorthy P. ;
Batra, Surinder K. .
STEM CELLS, 2018, 36 (09) :1329-1340
[47]   Induction of rod versus cone photoreceptor-specific progenitors from retinal precursor cells [J].
Khalili, Saeed ;
Ballios, Brian G. ;
Belair-Hickey, Justin ;
Donaldson, Laura ;
Liu, Jeff ;
Coles, Brenda L. K. ;
Grise, Kenneth N. ;
Baakdhah, Tahani ;
Bader, Gary D. ;
Wallace, Valerie A. ;
Bernier, Gilbert ;
Shoichet, Molly S. ;
van der Kooy, Derek .
STEM CELL RESEARCH, 2018, 33 :215-227
[48]   Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids [J].
Kim, Sangbae ;
Lowe, Albert ;
Dharmat, Rachayata ;
Lee, Seunghoon ;
Owen, Leah A. ;
Wang, Jun ;
Shakoor, Akbar ;
Li, Yumei ;
Morgan, Denise J. ;
Hejazi, Andre A. ;
Cvekl, Ales ;
DeAngelis, Margaret M. ;
Zhou, Z. Jimmy ;
Chen, Rui ;
Liu, Wei .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (22) :10824-10833
[49]   Stem cells in clinical trials for treatment of retinal degeneration [J].
Klassen, Henry .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2016, 16 (01) :7-14
[50]   Derivation and comparative assessment of retinal pigment epithelium from human embryonic stem cells using transcriptomics [J].
Klimanskaya, I ;
Hipp, J ;
Rezai, KA ;
West, M ;
Atala, A ;
Lanza, R .
CLONING AND STEM CELLS, 2004, 6 (03) :217-245