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Vectofusin-1,一种新的病毒进入增强子,可显著促进慢病毒对人造血干细胞的转导。

Vectofusin-1, a new viral entry enhancer, strongly promotes lentiviral transduction of human hematopoietic stem cells.

机构信息

1] Généthon, Evry, France [2] INSERM, UMR_S951, Généthon, Evry, France [3] Université Evry Val d'Essonne, UMR_S951, Evry, France.

出版信息

Mol Ther Nucleic Acids. 2013 May 7;2(5):e90. doi: 10.1038/mtna.2013.17.

Abstract

Gene transfer into hCD34(+) hematopoietic stem/progenitor cells (HSCs) using human immunodeficiency virus type 1 (HIV-1)-based lentiviral vectors (LVs) has several promising therapeutic applications. Yet, efficiency, safety, and cost of LV gene therapy could be ameliorated by enhancing target cell transduction levels and reducing the amount of LV used on the cells. Several transduction enhancers already exist such as fibronectin fragments and cationic compounds, but all present limitations. In this study, we describe a new transduction enhancer called Vectofusin-1, which is a short cationic peptide, active on several LV pseudotypes. Vectofusin-1 is used as a soluble additive to safely increase the frequency of transduced HSCs and to augment the level of transduction to one or two copies of vector per cell in a vector dose-dependent manner. Vectofusin-1 acts at the entry step by promoting the adhesion and the fusion between viral and cellular membranes. Vectofusin-1 is therefore a promising additive that could significantly ameliorate hCD34(+) cell-based gene therapy.Molecular Therapy-Nucleic Acids (2013) 2, e90; doi:10.1038/mtna.2013.17; published online 7 May 2013.

摘要

使用基于人类免疫缺陷病毒 1(HIV-1)的慢病毒载体(LVs)将基因转入人 CD34(+)造血干细胞/祖细胞(HSCs)具有多种很有前途的治疗应用。然而,通过提高靶细胞转导水平和减少细胞上使用的 LV 量,可以改善 LV 基因治疗的效率、安全性和成本。已经存在几种转导增强剂,如纤维连接蛋白片段和阳离子化合物,但都存在局限性。在这项研究中,我们描述了一种称为 Vectofusin-1 的新型转导增强剂,它是一种短的阳离子肽,对几种 LV 假型有效。Vectofusin-1 被用作可溶性添加剂,以安全地增加转导的 HSCs 的频率,并以载体剂量依赖性的方式增加每个细胞的转导水平至一个或两个拷贝的载体。Vectofusin-1 通过促进病毒和细胞膜之间的粘附和融合来在进入步骤中发挥作用。因此,Vectofusin-1 是一种很有前途的添加剂,可以显著改善基于 hCD34(+)细胞的基因治疗。分子治疗-核酸(2013)2,e90; doi:10.1038/mtna.2013.17; 2013 年 5 月 7 日在线发表。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ea6/4817938/041e66ca2104/mtna201317f1.jpg

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