Cell-based therapies for retinal diseases: a review of clinical trials and direct to consumer "cell therapy" clinics

被引:28
作者
Hinkle, John W. [1 ]
Mahmoudzadeh, Raziyeh [1 ]
Kuriyan, Ajay E. [1 ]
机构
[1] Thomas Jefferson Univ, Wills Eye Hosp, Mid Atlantic Retina, Philadelphia, PA 19107 USA
关键词
Age-related macular degeneration; Cell therapy clinics; Human embryonic stem cells; Human umbilical tissue-derived cells; Induced pluripotent stem cells; Retinal pigment epithelium; Stargardt's macular dystrophy; TISSUE-DERIVED CELLS; EMBRYONIC STEM-CELLS; INTRAVITREAL INJECTION; MACULAR DEGENERATION; VISION LOSS; GENERATION; RESOLUTION; SECONDARY; SURGERY;
D O I
10.1186/s13287-021-02546-9
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background The retinal pigment epithelium (RPE) is implicated in the pathophysiology of many retinal degenerative diseases. This cell layer is also an ideal target for cell-based therapies. Several early phase clinical trials evaluating cell therapy approaches for diseases involving the RPE, such as age-related macular degeneration and Stargardt's macular dystrophy have been published. However, there have also been numerous reports of complications from unproven "cell therapy" treatments marketed by "cell therapy" clinics. This review aims to outline the particular approaches in the different published clinical trials for cell-based therapies for retinal diseases. Additionally, the controversies surrounding experimental treatments offered outside of legitimate studies are presented. Main body Cell-based therapies can be applied to disorders that involve the RPE via a variety of techniques. A defining characteristic of any cell therapy treatment is the cell source used: human embryonic stem cells, induced pluripotent stem cells, and human umbilical tissue-derived cells have all been studied in published trials. In addition to the cell source, various trials have evaluated particular immunosuppression regiments, surgical approaches, and outcome measures. Data from early phase studies investigating cell-based therapies in non-neovascular age-related macular degeneration (70 patients, five trials), neovascular age-related macular degeneration (12 patients, four trials), and Stargardt's macular dystrophy (23 patients, three trials) have demonstrated safety related to the cell therapies, though evidence of significant efficacy has not been reported. This is in contrast to the multiple reports of serious complications and permanent vision loss in patients treated at "cell therapy" clinics. These interventions are marketed directly to patients, funded by the patient, lack Food and Drug Administration approval, and lack significant oversight. Conclusion Currently, there are no proven effective cell-based treatments for retinal diseases, although several trials have investigated potential therapies. These studies reported favorable safety profiles with multiple surgical approaches, with cells derived from multiple sources, and with utilized different immunosuppressive regiments. However, data demonstrating the efficacy and long-term safety are still pending. Nevertheless, "cell therapy" clinics continue to conduct direct-to consumer marketing for non-FDA-approved treatments with potentially blinding complications.
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页数:9
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共 44 条
[1]   Brain-derived neurotrophic factor produced by human umbilical tissue-derived cells is required for its effect on hippocampal dendritic differentiation [J].
Alder, Janet ;
Kramer, Brian C. ;
Hoskin, Casey ;
Thakker-Varia, Smita .
DEVELOPMENTAL NEUROBIOLOGY, 2012, 72 (06) :755-765
[2]  
Astellas Institute for Regenerative Medicine, 2017, REPORT NO NCT0146983
[3]  
Astellas Institute for Regenerative Medicine, 2017, REPORT NO NCT0134500
[4]  
Astellas Institute for Regenerative Medicine, 2017, REPORT NO NCT0134499
[5]   Induced pluripotent stem cell-based therapy for age-related macular degeneration [J].
Bracha, Peter ;
Moore, Nicholas A. ;
Ciulla, Thomas A. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2017, 17 (09) :1113-1126
[6]   Human Umbilical Tissue-Derived Cells Rescue Retinal Pigment Epithelium Dysfunction in Retinal Degeneration [J].
Cao, Jing ;
Murat, Christopher ;
An, Weijun ;
Yao, Xiang ;
Lee, John ;
Santulli-Marotto, Sandra ;
Harris, Ian R. ;
Inana, George .
STEM CELLS, 2016, 34 (02) :367-379
[7]  
CHABiotech CO. Ltd, 2019, REPORT NO NCT0167482
[8]   Phase 1 clinical study of an embryonic stem cell-derived retinal pigment epithelium patch in age-related macular degeneration [J].
da Cruz, Lyndon ;
Fynes, Kate ;
Georgiadis, Odysseas ;
Kerby, Julie ;
Luo, Yvonne H. ;
Ahmado, Ahmad ;
Vernon, Amanda ;
Daniels, Julie T. ;
Nommiste, Britta ;
Hasan, Shazeen M. ;
Gooljar, Sakina B. ;
Carr, Amanda-Jayne F. ;
Vugler, Anthony ;
Ramsden, Conor M. ;
Bictash, Magda ;
Fenster, Mike ;
Steer, Juliette ;
Harbinson, Tricia ;
Wilbrey, Anna ;
Tufail, Adnan ;
Feng, Gang ;
Whitlock, Mark ;
Robson, Anthony G. ;
Holder, Graham E. ;
Sagoo, Mandeep S. ;
Loudon, Peter T. ;
Whiting, Paul ;
Coffey, Peter J. .
NATURE BIOTECHNOLOGY, 2018, 36 (04) :1-+
[9]   Effect of sham surgery on retinal function after subretinal transplantation of the artificial silicone retina [J].
Del Priore, LV .
ARCHIVES OF OPHTHALMOLOGY, 2005, 123 (08) :1156-1156
[10]   Xenotransplantation of retinal pigment epithelial cells into RCS rats [J].
Grisanti, S ;
Szurman, P ;
Jordan, J ;
Kociok, N ;
Bartz-Schmidt, KU ;
Heimann, K .
JAPANESE JOURNAL OF OPHTHALMOLOGY, 2002, 46 (01) :36-44