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开发具有改进安全性特征的新型高效 SIN 载体,用于基于 Wiskott-Aldrich 综合征干细胞的基因治疗。

Development of novel efficient SIN vectors with improved safety features for Wiskott-Aldrich syndrome stem cell based gene therapy.

机构信息

Department of Pediatric Hematology/Oncology, Hannover Medical School, Hannover, Germany.

出版信息

Mol Pharm. 2011 Oct 3;8(5):1525-37. doi: 10.1021/mp200132u. Epub 2011 Aug 31.

Abstract

Gene therapy is a promising therapeutic approach to treat primary immunodeficiencies. Indeed, the clinical trial for the Wiskott-Aldrich Syndrome (WAS) that is currently ongoing at the Hannover Medical School (Germany) has recently reported the correction of all affected cell lineages of the hematopoietic system in the first treated patients. However, an extensive study of the clonal inventory of those patients reveals that LMO2, CCND2 and MDS1/EVI1 were preferentially prevalent. Moreover, a first leukemia case was observed in this study, thus reinforcing the need of developing safer vectors for gene transfer into HSC in general. Here we present a novel self-inactivating (SIN) vector for the gene therapy of WAS that combines improved safety features. We used the elongation factor 1 alpha (EFS) promoter, which has been extensively evaluated in terms of safety profile, to drive a codon-optimized human WASP cDNA. To test vector performance in a more clinically relevant setting, we transduced murine HSPC as well as human CD34+ cells and also analyzed vector efficacy in their differentiated myeloid progeny. Our results show that our novel vector generates comparable WAS protein levels and is as effective as the clinically used LTR-driven vector. Therefore, the described SIN vectors appear to be good candidates for potential use in a safer new gene therapy protocol for WAS, with decreased risk of insertional mutagenesis.

摘要

基因治疗是治疗原发性免疫缺陷的一种有前途的治疗方法。事实上,目前正在德国汉诺威医学院进行的威斯科特-奥尔德里奇综合征(WAS)的临床试验最近报告称,第一批接受治疗的患者的造血系统所有受影响的细胞谱系都得到了纠正。然而,对这些患者的克隆库存进行的广泛研究表明,LMO2、CCND2 和 MDS1/EVI1 更为普遍。此外,在这项研究中观察到首例白血病病例,因此需要开发更安全的载体,将基因转移到造血干细胞中。在这里,我们提出了一种用于 WAS 基因治疗的新型自失活(SIN)载体,该载体结合了改进的安全性特征。我们使用了延伸因子 1 阿尔法(EFS)启动子,该启动子在安全性方面已经得到了广泛的评估,以驱动密码子优化的人类 WASP cDNA。为了在更具临床相关性的环境中测试载体的性能,我们转导了鼠 HSPC 以及人 CD34+细胞,并分析了它们在分化的髓系祖细胞中的载体功效。我们的结果表明,我们的新型载体产生了可比的 WAS 蛋白水平,并且与临床使用的 LTR 驱动载体一样有效。因此,所描述的 SIN 载体似乎是一种潜在的候选物,可用于更安全的新 WAS 基因治疗方案,降低插入突变的风险。

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