Toward cell replacement therapy: promises and caveats

被引:32
作者
Ginis, I [1 ]
Rao, MS [1 ]
机构
[1] NIA, Gerontol Res Ctr, Stem Cell Biol Unit, Neurosci Lab,NIH, Baltimore, MD 21224 USA
关键词
transplantation; neurons; glia; neural precursors; mouse models; immune response; allelic variability; clinical trials; neurological disease;
D O I
10.1016/S0014-4886(03)00256-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Studies in animal models have suggested a role for stem cells in repair and regeneration of the nervous system. Human equivalents of stem and precursor cells have been isolated and their efficacy is being evaluated in rodent and primate models. Difficulties exist in translating results of these preclinical models to therapy in humans. Evolutionary differences among rodents, primates, and humans; fundamental differences in the anatomy and physiology; differences in immune responses in xenotransplant models; the paucity of good transplant models of chronic disease; and allelic variability in the cells themselves make any study evaluating the efficacy of cells in transplant models difficult to interpret. As no better alternatives to testing in animals exist, we suggest that at this early stage a considered step-by-step approach to testing and comparison of different transplant strategies in isolation will prepare us better for clinical trials than simple evaluation of functional outcomes in various models of disease. We emphasize that we do not recommend delaying or abandoning clinical trials; rather, we suggest that one anticipate failures and design experiments and data collection such that we learn from these failures to ensure future success in as rapid a time frame as possible. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:61 / 77
页数:17
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