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Impaired Arm Function and Finger Dexterity in a Nonhuman Primate Model of Stroke: Motor and Cognitive Assessments.中风非人灵长类动物模型中的手臂功能和手指灵活性受损:运动和认知评估
Stroke. 2016 Apr;47(4):1109-16. doi: 10.1161/STROKEAHA.115.012506. Epub 2016 Mar 8.
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Long-term glycemic control using polymer-encapsulated human stem cell-derived beta cells in immune-competent mice.在具有免疫活性的小鼠中使用聚合物封装的人干细胞衍生的β细胞进行长期血糖控制。
Nat Med. 2016 Mar;22(3):306-11. doi: 10.1038/nm.4030. Epub 2016 Jan 25.
3
Insulin-Producing Endocrine Cells Differentiated In Vitro From Human Embryonic Stem Cells Function in Macroencapsulation Devices In Vivo.体外从人胚胎干细胞分化而来的胰岛素分泌内分泌细胞在体内的大封装装置中发挥功能。
Stem Cells Transl Med. 2015 Oct;4(10):1214-22. doi: 10.5966/sctm.2015-0079. Epub 2015 Aug 24.
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Successful pharmaceutical-grade streptozotocin (STZ)-induced hyperglycemia in a conscious tethered baboon (Papio hamadryas) model.在有意识的束缚狒狒(阿拉伯狒狒)模型中成功诱导出药物级链脲佐菌素(STZ)所致的高血糖症。
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Human embryonic-stem-cell-derived cardiomyocytes regenerate non-human primate hearts.人类胚胎干细胞衍生的心肌细胞可使非人类灵长类动物的心脏再生。
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Scientific Rigor Recommendations for Optimizing the Clinical Applicability of Translational Research.优化转化研究临床适用性的科学严谨性建议。
J Neurol Neurophysiol. 2012;3. doi: 10.4172/2155-9562.1000e111.
7
Direct comparison of autologous and allogeneic transplantation of iPSC-derived neural cells in the brain of a non-human primate.自体和异体 iPSC 源性神经细胞移植于非人类灵长类动物脑内的直接比较。
Stem Cell Reports. 2013 Sep 26;1(4):283-92. doi: 10.1016/j.stemcr.2013.08.007. eCollection 2013.
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Long-term clinical outcome of fetal cell transplantation for Parkinson disease: two case reports.胎儿细胞移植治疗帕金森病的长期临床疗效:两例报告
JAMA Neurol. 2014 Jan;71(1):83-7. doi: 10.1001/jamaneurol.2013.4749.
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Intracerebral transplantation of differentiated human embryonic stem cells to hemiparkinsonian monkeys.脑内移植分化的人胚胎干细胞到偏侧帕金森病猴。
Cell Transplant. 2013;22(5):831-8. doi: 10.3727/096368912X647144.
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Induced pluripotent stem cell-derived neural cells survive and mature in the nonhuman primate brain.诱导多能干细胞衍生的神经细胞在非人类灵长类动物大脑中存活和成熟。
Cell Rep. 2013 Mar 28;3(3):646-50. doi: 10.1016/j.celrep.2013.02.016. Epub 2013 Mar 14.

用于干细胞治疗疾病临床建模的非人灵长类动物模型。

Nonhuman primate model in clinical modeling of diseases for stem cell therapy.

作者信息

Choudhury Gourav R, Kim Jeffrey, Frost Patrice A, Bastarrachea Raul A, Daadi Marcel M

机构信息

Southwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, Texas, USA.

Department of Cellular and Structural Biology, UT Health Science Center, San Antonio, Texas, USA.

出版信息

Brain Circ. 2016 Jul-Sep;2(3):141-145. doi: 10.4103/2394-8108.192524. Epub 2016 Oct 18.

DOI:10.4103/2394-8108.192524
PMID:30276291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6126269/
Abstract

Nonhuman primates (NHPs) are alike humans in size, behavior, physiology, biochemistry, and immunology. Given close similarities to humans, the NHP model offers exceptional opportunities to understand the biological mechanisms and translational applications with direct relevance to human conditions. Here, we evaluate the opportunities and limitations of NHPs as animal models for translational regenerative medicine. NHP models of human disease propose exceptional opportunities to advance stem cell-based therapy by addressing pertinent translational concerns related to this research. Nonetheless, the value of these primates must be carefully assessed, taking into account the expense of specialized equipment and requirement of highly specialized staff. Well-designed initial fundamental studies in small animal models are essential before translating research into NHP models and eventually into human trials. In addition, we suggest that applying a directed and collaborative approach, as seen in the evolution of stroke NHP models, will greatly benefit the translation of stem cell therapy in other NHP disease models.

摘要

非人灵长类动物(NHPs)在体型、行为、生理学、生物化学和免疫学方面与人类相似。鉴于与人类的密切相似性,NHP模型为理解与人类疾病直接相关的生物学机制和转化应用提供了绝佳机会。在此,我们评估NHP作为转化再生医学动物模型的机会和局限性。人类疾病的NHP模型通过解决与该研究相关的相关转化问题,为推进基于干细胞的治疗提供了绝佳机会。尽管如此,必须仔细评估这些灵长类动物的价值,同时考虑到专用设备的成本和对高度专业化工作人员的要求。在将研究转化为NHP模型并最终转化为人体试验之前,在小动物模型中进行精心设计的初始基础研究至关重要。此外,我们建议采用一种定向且协作的方法,就像在中风NHP模型的发展过程中所看到的那样,这将极大地有利于干细胞治疗在其他NHP疾病模型中的转化。