首页> 美国卫生研究院文献>Molecular Therapy >Repeated Mesenchymal Stromal Cell Treatment Sustainably Alleviates Machado-Joseph Disease
【2h】

Repeated Mesenchymal Stromal Cell Treatment Sustainably Alleviates Machado-Joseph Disease

机译:反复间充质基质细胞治疗可持续缓解马查多-约瑟夫病

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3, the most common dominant spinocerebellar ataxia (SCA) worldwide, is caused by over-repetition of a CAG repeat in the ATXN3/MJD1 gene, which translates into a polyglutamine tract within the ataxin-3 protein. There is no treatment for this fatal disorder. Despite evidence of the safety and efficacy of mesenchymal stromal cells (MSCs) in delaying SCA disease progression in exploratory clinical trials, unanticipated regression of patients to the status prior to treatment makes the investigation of causes and solutions urgent and imperative. In the present study, we compared the efficacy of a single intracranial injection with repeated systemic MSC administration in alleviating the MJD phenotype of two strongly severe genetic rodent models. We found that a single MSC transplantation only produces transient effects, whereas periodic administration promotes sustained motor behavior and neuropathology alleviation, suggesting that MSC therapies should be re-designed to get sustained beneficial results in clinical practice. Furthermore, MSC promoted neuroprotection, increased the levels of GABA and glutamate, and decreased the levels of Myo-inositol, which correlated with motor improvements, indicating that these metabolites may serve as valid neurospectroscopic biomarkers of disease and treatment. This study makes important contributions to the design of new clinical approaches for MJD and other SCAs/polyglutamine disorders.
机译:Machado-Joseph病(MJD)或3型脊髓小脑共济失调(全世界最常见的脊髓小脑共济失调(SCA))是由ATXN3 / MJD1基因中CAG重复序列的过度重复引起的,该基因转化为紫杉醇内的多聚谷氨酰胺-3蛋白。没有针对这种致命疾病的治疗方法。尽管在探索性临床试验中有证据表明间充质基质细胞(MSCs)可以延缓SCA疾病的发展,但其安全性和有效性已得到证实,但是,患者意外退缩至治疗前的状况使得对原因和解决方案的研究变得迫在眉睫。在本研究中,我们比较了一次颅内注射与重复全身性MSC给药在缓解两个强效遗传啮齿动物模型的MJD表型方面的功效。我们发现单次MSC移植只会产生短暂的效果,而定期给药则可以促进持续的运动行为和神经病理学缓解,这表明应该重新设计MSC疗法以在临床实践中获得持续的有益效果。此外,MSC促进了神经保护,增加了GABA和谷氨酸的水平,并降低了肌醇的水平,这与运动能力的改善相关,表明这些代谢物可作为疾病和治疗的有效神经光谱生物标志物。这项研究为MJD和其他SCA /多谷氨酰胺疾病的新临床方法设计做出了重要贡献。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号