Targeted Delivery and Tolerability of MRI-Guided CED Infusion into the Cerebellum of Nonhuman Primates.

Q1 Immunology and Microbiology Human Gene Therapy Methods Pub Date : 2018-08-01 Epub Date: 2018-08-13 DOI:10.1089/hgtb.2018.049
Ernesto A Salegio, Michael V Campagna, Philip C Allen, Diane E Stockinger, Yuanquan Song, Granger G C Hwa
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引用次数: 1

Abstract

This study explored the feasibility of intraparenchymal delivery (gadoteridol and/or Serotype 5 Adeno-Associated Viral Vector-enhanced Green Fluorescent Protein [AAV5-eGFP]) into the cerebellum of nonhuman primates using real-time magnetic resonance imaging-guided convection enhanced delivery (MRI-CED) technology. All animals tolerated the neurosurgical procedure without any clinical sequela. Gene expression was detected within the cerebellar parenchyma at the site of infusion and resulted in transduction of neuronal cell bodies and fibers. Histopathology indicated localized damage along the stem of the cannula tract. These findings demonstrate the potential of real-time MRI-CED to deliver therapeutics into the cerebellum, which has extensive reciprocal connections and may be used as a target for the treatment of neurological disorders.

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非人类灵长类动物小脑mri引导下CED输注的靶向递送和耐受性。
本研究探讨了利用实时磁共振成像引导对流增强递送(MRI-CED)技术,将肺实质内递送(gadoteridol和/或血清型5腺相关病毒载体增强型绿色荧光蛋白[AAV5-eGFP])送入非人灵长类动物小脑的可行性。所有动物都能耐受神经外科手术,没有任何临床后遗症。在输注部位的小脑实质内检测到基因表达,并导致神经元细胞体和纤维的转导。组织病理学显示沿管束茎部局部损伤。这些发现证明了实时MRI-CED将治疗药物输送到小脑的潜力,小脑具有广泛的相互连接,可能被用作治疗神经系统疾病的靶点。
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来源期刊
Human Gene Therapy Methods
Human Gene Therapy Methods BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Human Gene Therapy is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes in-depth coverage of DNA, RNA, and cell therapies by delivering the latest breakthroughs in research and technologies. Human Gene Therapy provides a central forum for scientific and clinical information, including ethical, legal, regulatory, social, and commercial issues, which enables the advancement and progress of therapeutic procedures leading to improved patient outcomes, and ultimately, to curing diseases. The Journal is divided into three parts. Human Gene Therapy, the flagship, is published 12 times per year. HGT Methods, a bimonthly journal, focuses on the applications of gene therapy to product testing and development. HGT Clinical Development, a quarterly journal, serves as a venue for publishing data relevant to the regulatory review and commercial development of cell and gene therapy products.
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