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本文引用的文献

1
Stem Cell Ophthalmology Treatment Study (SCOTS): bone marrow-derived stem cells in the treatment of Leber's hereditary optic neuropathy.干细胞眼科治疗研究(SCOTS):骨髓源性干细胞治疗Leber遗传性视神经病变
Neural Regen Res. 2016 Oct;11(10):1685-1694. doi: 10.4103/1673-5374.193251.
2
EPIRETINAL MEMBRANE FORMATION AFTER INTRAVITREAL AUTOLOGOUS STEM CELL IMPLANTATION IN A RETINITIS PIGMENTOSA PATIENT.视网膜色素变性患者玻璃体内自体干细胞植入术后的视网膜前膜形成
Retin Cases Brief Rep. 2017;11(3):227-231. doi: 10.1097/ICB.0000000000000327.
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Stem Cell Ophthalmology Treatment Study (SCOTS) for retinal and optic nerve diseases: a case report of improvement in relapsing auto-immune optic neuropathy.视网膜和视神经疾病的干细胞眼科治疗研究(SCOTS):复发性自身免疫性视神经病变改善的病例报告
Neural Regen Res. 2015 Sep;10(9):1507-15. doi: 10.4103/1673-5374.165525.
4
Stem Cell Ophthalmology Treatment Study (SCOTS) for retinal and optic nerve diseases: a preliminary report.干细胞眼科治疗研究(SCOTS)治疗视网膜和视神经疾病:初步报告。
Neural Regen Res. 2015 Jun;10(6):982-8. doi: 10.4103/1673-5374.158365.
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Paracrine Factors Secreted by MSCs Promote Astrocyte Survival Associated With GFAP Downregulation After Ischemic Stroke via p38 MAPK and JNK.间充质干细胞分泌的旁分泌因子通过p38丝裂原活化蛋白激酶和c-Jun氨基末端激酶促进缺血性中风后与胶质纤维酸性蛋白下调相关的星形胶质细胞存活。
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Stem cell treatment of degenerative eye disease.干细胞治疗退行性眼病。
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Immunomodulatory role of microRNAs transferred by extracellular vesicles.细胞外囊泡转运的微小RNA的免疫调节作用
Biol Cell. 2015 Mar;107(3):61-77. doi: 10.1111/boc.201400081. Epub 2015 Feb 12.
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Distribution of mesenchymal stem cells and effects on neuronal survival and axon regeneration after optic nerve crush and cell therapy.视神经挤压伤及细胞治疗后间充质干细胞的分布及其对神经元存活和轴突再生的影响
PLoS One. 2014 Oct 27;9(10):e110722. doi: 10.1371/journal.pone.0110722. eCollection 2014.
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Paracrine-mediated neuroprotection and neuritogenesis of axotomised retinal ganglion cells by human dental pulp stem cells: comparison with human bone marrow and adipose-derived mesenchymal stem cells.人牙髓干细胞旁分泌介导的视网膜神经节细胞轴突切断后的神经保护和神经突生成:与人类骨髓和脂肪来源的间充质干细胞的比较
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Medical management of hereditary optic neuropathies.遗传性视神经病变的医学管理
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干细胞眼科治疗研究(SCOTS):骨髓来源的干细胞治疗显性遗传性视神经萎缩

Stem Cell Ophthalmology Treatment Study (SCOTS): bone marrow derived stem cells in the treatment of Dominant Optic Atrophy.

作者信息

Weiss Jeffrey N, Levy Steven

机构信息

The Healing Institute, Margate, FL, USA.

MD Stem Cells, Westport, CT, USA.

出版信息

Stem Cell Investig. 2019 Dec 5;6:41. doi: 10.21037/sci.2019.11.01. eCollection 2019.

DOI:10.21037/sci.2019.11.01
PMID:32039263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6987313/
Abstract

BACKGROUND

We report the results of 6 patients with Dominant Optic Atrophy (DOA) who met inclusion criteria and were treated in the Stem Cell Ophthalmology Treatment Study (SCOTS). SCOTS/SCOTS 2 is an Institutional Review Board approved and NIH registered (NCT03011541) clinical study that uses autologous bone marrow derived stem cells (BMSC) in the treatment of optic nerve and retinal disease.

METHODS

This is an open label, non-randomized clinical study using natural history of the disease as the comparator. BMSC were separated from aspirated autologous bone marrow with minimal manipulation using an FDA cleared Class II medical device. Patients were treated with combinations of retrobulbar, subtenons, intravitreal or subretinal placement of BMSC followed by intravenous injection of BMSC depending on the arm of the study chosen. There were no surgical complications.

RESULTS

Of the patients treated, 83.3% (5 of 6 patients) experienced visual improvements and in all of these cases both eyes improved. Ten eyes or 83.3% experienced gains in visual acuity with a median improvement of 2.125 Snellen lines, or approximately 10.63 letters. Two eyes were considered unchanged compared to longstanding measurements. Using LogMAR, the average improvement in vision for all eyes was 29.5%. The averagevisual acuity increasein eyes that improved was 33.3%. Findings were statistically significant with P<0.001.

CONCLUSIONS

Using autologous BMSC per protocols developed in the SCOTS/SCOTS 2 clinical studies resulted in statistically significant visual acuity improvements in patients with DOA or Kjers Optic Neuropathy. Improvements occurred in 83.3% of eyes and averaged 29.5%. Mitochondrial transfer and neuroprotective exosome secretions from the BMSC may have been key to the improvements observed in this mitochondrial disease.

摘要

背景

我们报告了6例符合纳入标准并在干细胞眼科治疗研究(SCOTS)中接受治疗的显性遗传性视神经萎缩(DOA)患者的结果。SCOTS/SCOTS 2是一项经机构审查委员会批准并在美国国立卫生研究院注册(NCT03011541)的临床研究,该研究使用自体骨髓来源的干细胞(BMSC)治疗视神经和视网膜疾病。

方法

这是一项开放标签、非随机的临床研究,以疾病的自然病程作为对照。使用经美国食品药品监督管理局批准的II类医疗设备,通过最少的操作从抽取的自体骨髓中分离出BMSC。根据所选研究组,患者接受球后、腱下、玻璃体内或视网膜下注射BMSC的联合治疗,随后静脉注射BMSC。未出现手术并发症。

结果

在接受治疗的患者中,83.3%(6例中的5例)视力得到改善,且所有这些病例的双眼均有改善。10只眼(即83.3%)视力提高,平均提高2.125行斯内伦视力表视力,约相当于10.63个字母。与长期测量结果相比,有2只眼被认为无变化。使用最小分辨角对数视力表(LogMAR),所有眼睛的平均视力改善为29.5%。视力改善的眼睛平均视力提高33.3%。结果具有统计学意义,P<0.001。

结论

按照SCOTS/SCOTS 2临床研究制定的方案使用自体BMSC,可使DOA或凯尔氏视神经病变患者的视力得到具有统计学意义的改善。83.3%的眼睛视力得到改善,平均改善率为29.5%。BMSC的线粒体转移和神经保护性外泌体分泌可能是在这种线粒体疾病中观察到改善的关键。