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Stroke. 2009 Mar;40(3 Suppl):S146-8. doi: 10.1161/STROKEAHA.108.533091. Epub 2008 Dec 8.
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Who's in favor of translational cell therapy for stroke: STEPS forward please?有谁支持中风的转化细胞治疗:请举手示意?
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本文引用的文献

1
Stem Cell Therapies as an Emerging Paradigm in Stroke (STEPS): bridging basic and clinical science for cellular and neurogenic factor therapy in treating stroke.干细胞疗法作为中风治疗的新兴范式(STEPS):为中风的细胞和神经源性因子治疗搭建基础科学与临床科学的桥梁。
Stroke. 2009 Feb;40(2):510-5. doi: 10.1161/STROKEAHA.108.526863. Epub 2008 Dec 18.
2
Potential of stem/progenitor cells in treating stroke: the missing steps in translating cell therapy from laboratory to clinic.干细胞/祖细胞治疗中风的潜力:将细胞疗法从实验室转化到临床过程中缺失的环节。
Regen Med. 2008 May;3(3):249-50. doi: 10.2217/17460751.3.3.249.
3
Severity of leukoaraiosis and susceptibility to infarct growth in acute stroke.急性卒中患者脑白质疏松症的严重程度与梗死灶扩大的易感性
Stroke. 2008 May;39(5):1409-13. doi: 10.1161/STROKEAHA.107.501932. Epub 2008 Mar 13.
4
Responses of endothelial cell and astrocyte matrix-integrin receptors to ischemia mimic those observed in the neurovascular unit.内皮细胞和星形胶质细胞基质整合素受体对缺血的反应与在神经血管单元中观察到的反应相似。
Stroke. 2008 Jan;39(1):191-7. doi: 10.1161/STROKEAHA.107.486134. Epub 2007 Nov 21.
5
Hippocampal CA1 cell loss in a non-human primate model of transient global ischemia: a pilot study.短暂性全脑缺血非人类灵长类动物模型中海马CA1区细胞损失:一项初步研究。
Brain Res Bull. 2007 Sep 14;74(1-3):164-71. doi: 10.1016/j.brainresbull.2007.06.014.
6
Niaspan increases angiogenesis and improves functional recovery after stroke.烟酸缓释片可促进中风后的血管生成并改善功能恢复。
Ann Neurol. 2007 Jul;62(1):49-58. doi: 10.1002/ana.21160.
7
Long-term monitoring of transplanted human neural stem cells in developmental and pathological contexts with MRI.利用磁共振成像对发育和病理环境下移植的人神经干细胞进行长期监测。
Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10211-6. doi: 10.1073/pnas.0608519104. Epub 2007 Jun 6.
8
Transplantation of bone marrow-derived stem cells: a promising therapy for stroke.骨髓源性干细胞移植:一种有前景的中风治疗方法。
Cell Transplant. 2007;16(2):159-69.
9
Making stem cell lines suitable for transplantation.
Cell Transplant. 2007;16(2):101-15.
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Pattern of cortex and white matter involvement in severe middle cerebral artery ischemia.大脑中动脉严重缺血时皮质和白质受累模式
J Neuroimaging. 2007 Apr;17(2):131-40. doi: 10.1111/j.1552-6569.2007.00102.x.

中风的细胞治疗:开展临床试验前有待解决的遗留问题。

Cell therapy for stroke: remaining issues to address before embarking on clinical trials.

作者信息

Borlongan Cesar V

机构信息

Department of Neurology, Medical College of Georgia, BI-3080, Augusta, GA 30912, USA.

出版信息

Stroke. 2009 Mar;40(3 Suppl):S146-8. doi: 10.1161/STROKEAHA.108.533091. Epub 2008 Dec 8.

DOI:10.1161/STROKEAHA.108.533091
PMID:19064801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4810678/
Abstract

BACKGROUND AND PURPOSE

Stroke remains a significant clinical unmet condition, with only 3% of ischemic patient population benefiting from the thrombolytic drug tissue plasminogen activator largely because of the drug's narrow 3-hour therapeutic window. Extending the stroke therapeutic window will greatly impact on treatment, care, and management of patients. Summary of Review- Cell therapy is appealing in this regard as it widens the stroke treatment opportunity by targeting the neurorestorative phase (ie, several hours to days and even weeks or months after stroke). Although compelling preclinical evidence reveals that transplantation of stem/progenitor cells is safe and effective in animal models of stroke, the laboratory data need to be evaluated on their translational relevance for clinical application. In addressing this issue, I borrow heavily from the conference proceedings of the 2007 STEPS (Stem Cell Therapeutics as an Emerging Paradigm in Stroke).

CONCLUSIONS

Translational research guidelines are being adapted by academic institutes, industry, National Institutes of Health (NIH), and Food and Drug Administration (FDA), and adhering to these preclinical criteria will provide the basis for advancing cell therapy in stroke from the laboratory to the clinic.

摘要

背景与目的

中风仍然是一个尚未得到有效临床解决的重大问题,仅有3%的缺血性中风患者能从溶栓药物组织型纤溶酶原激活剂中获益,这主要是因为该药物的治疗窗口期仅3小时,非常狭窄。延长中风治疗窗口期将对患者的治疗、护理及管理产生重大影响。综述总结——在这方面,细胞疗法颇具吸引力,因为它通过针对神经修复阶段(即中风后数小时至数天甚至数周或数月)拓宽了中风治疗机会。尽管有令人信服的临床前证据表明,在中风动物模型中,干细胞/祖细胞移植是安全有效的,但这些实验室数据的临床转化相关性仍需评估。在解决这个问题时,我大量借鉴了2007年“干细胞疗法作为中风新范例”(STEM)会议的会议记录。

结论

学术机构、产业界、美国国立卫生研究院(NIH)和美国食品药品监督管理局(FDA)正在调整转化研究指南,遵循这些临床前标准将为把中风细胞疗法从实验室推进到临床提供基础。