Stem cells in clinical trials for treatment of retinal degeneration

被引:57
作者
Klassen, Henry [1 ,2 ]
机构
[1] Univ Calif Irvine, Gavin Herbert Eye Inst, Sue & Bill Gross Hall,Room 2006,845 Hlth Sci Rd, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Stem Cell Res Ctr, Sue & Bill Gross Hall,Room 2006,845 Hlth Sci Rd, Irvine, CA 92697 USA
关键词
age-related macular degeneration; cell-based; intravitreal; photoreceptor; progenitor; retinal pigment epithelial; retinitis pigmentosa; Stargardt; subretinal; transplantation; RETINITIS-PIGMENTOSA PATIENTS; PROGENITOR CELLS; MACULAR DEGENERATION; INTRAVITREAL USE; VISUAL FUNCTION; RCS RAT; TRANSPLANTATION; EPITHELIUM; RPE; RESCUE;
D O I
10.1517/14712598.2016.1093110
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: After decades of basic science research involving the testing of regenerative strategies in animal models of retinal degenerative diseases, a number of clinical trials are now underway, with additional trials set to begin shortly. These efforts will evaluate the safety and preliminary efficacy of cell-based products in the eyes of patients with a number of retinal conditions, notably including age-related macular degeneration, retinitis pigmentosa and Stargardt's disease.Areas covered: This review considers the scientific work and early trials with fetal cells and tissues that set the stage for the current clinical investigatory work, as well the trials themselves, specifically those either now completed, underway or close to initiation. The cells of interest include retinal pigment epithelial cells derived from embryonic stem or induced pluripotent stem cells, undifferentiated neural or retinal progenitors or cells from the vascular/bone marrow compartment or umbilical cord tissue.Expert opinion: Degenerative diseases of the retina represent a popular target for emerging cell-based therapeutics and initial data from early stage clinical trials suggest that short-term safety objectives can be met in at least some cases. The question of efficacy will require additional time and testing to be adequately resolved.
引用
收藏
页码:7 / 14
页数:8
相关论文
共 53 条
[1]   Long-term outcome of RPE allografts in non-immunosuppressed patients with AMD [J].
Algvere, PV ;
Gouras, P ;
Kopp, ED .
EUROPEAN JOURNAL OF OPHTHALMOLOGY, 1999, 9 (03) :217-230
[2]   Transplantation of RPE in age-related macular degeneration: Observations in disciform lesions and dry RPE atrophy [J].
Algvere, PV ;
Berglin, L ;
Gouras, P ;
Sheng, YH ;
Kopp, ED .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1997, 235 (03) :149-158
[3]  
[Anonymous], 2014, NEWS NATURE
[4]  
ARAMANT R, 1990, RESTOR NEUROL NEUROS, V2, P9, DOI 10.3233/RNN-1990-2102
[5]  
BioTime's Subsidiary Cell Cure Neurosciences Ltd, 2015, AW 1 6 MILL GRANT IS
[6]   FUNCTIONAL REACTIVATION OF THE DEAFFERENTED NEOSTRIATUM BY NIGRAL TRANSPLANTS [J].
BJORKLUND, A ;
STENEVI, U ;
DUNNETT, SB ;
IVERSEN, SD .
NATURE, 1981, 289 (5797) :497-499
[7]  
Blenkinsop Timothy A, 2013, Methods Mol Biol, V945, P45, DOI 10.1007/978-1-62703-125-7_4
[8]   Derivation of Functional Retinal Pigmented Epithelium from Induced Pluripotent Stem Cells [J].
Buchholz, David E. ;
Hikita, Sherry T. ;
Rowland, Teisha J. ;
Friedrich, Amy M. ;
Hinman, Cassidy R. ;
Johnson, Lincoln V. ;
Clegg, Dennis O. .
STEM CELLS, 2009, 27 (10) :2427-2434
[9]  
ClinicalTrials, 2015, STUD HUM CENTR NERV
[10]  
ClinicalTrials. gov A service of the National Institutes of Health, 2015, STUD HUCNS SC SUBR T