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溶酶体贮积病中枢神经系统的干细胞治疗

Stem Cell Therapy for the Central Nervous System in Lysosomal Storage Diseases.

作者信息

Siddiqi Faez, Wolfe John H

机构信息

1 Research Institute of Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

2 Department of Pediatrics, Perelman School of Medicine and W.F. Goodman Center for Comparative Medical Genetics, School of Veterinary Medicine, University of Pennsylvania , Philadelphia, Pennsylvania.

出版信息

Hum Gene Ther. 2016 Oct;27(10):749-757. doi: 10.1089/hum.2016.088. Epub 2016 Jul 13.

Abstract

Neurological diseases with genetic etiologies result in the loss or dysfunction of neural cells throughout the CNS. At present, few treatment options exist for the majority of neurogenetic diseases. Stem cell transplantation (SCT) into the CNS has the potential to be an effective treatment modality because progenitor cells may replace lost cells in the diseased brain, provide multiple trophic factors, or deliver missing proteins. This review focuses on the use of SCT in lysosomal storage diseases (LSDs), a large group of monogenic disorders with prominent CNS disease. In most patients the CNS disease results in intellectual disability that is refractory to current standard-of-care treatment. A large amount of preclinical work on brain-directed SCT has been performed in rodent LSD models. Cell types that have been used for direct delivery into the CNS include neural stem cells, embryonic and induced pluripotent stem cells, and mesenchymal stem cells. Hematopoietic stem cells have been an effective therapy for the CNS in a few LSDs and may be augmented by overexpression of the missing gene. Current barriers and potential strategies to improve SCT for translation into effective patient therapies are discussed.

摘要

具有遗传病因的神经系统疾病会导致整个中枢神经系统(CNS)神经细胞的丧失或功能障碍。目前,大多数神经遗传疾病几乎没有治疗选择。将干细胞移植(SCT)到中枢神经系统有可能成为一种有效的治疗方式,因为祖细胞可以替代患病大脑中丢失的细胞,提供多种营养因子,或递送缺失的蛋白质。本综述重点关注干细胞移植在溶酶体贮积症(LSDs)中的应用,溶酶体贮积症是一大类具有突出中枢神经系统疾病的单基因疾病。在大多数患者中,中枢神经系统疾病会导致智力残疾,而目前的标准治疗方法对此无效。在啮齿动物溶酶体贮积症模型中已经开展了大量针对脑靶向干细胞移植的临床前研究。已用于直接递送至中枢神经系统的细胞类型包括神经干细胞、胚胎干细胞和诱导多能干细胞以及间充质干细胞。造血干细胞已成为少数几种溶酶体贮积症中枢神经系统疾病的有效治疗方法,并且可以通过缺失基因的过表达来增强疗效。本文还讨论了目前的障碍以及将干细胞移植转化为有效的患者治疗方法的潜在策略。

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