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对转基因编码蛋白的免疫反应限制了注射复制缺陷型腺病毒载体后基因表达的稳定性。

Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors.

作者信息

Tripathy S K, Black H B, Goldwasser E, Leiden J M

机构信息

Department of Pathology, University of Chicago, Illinois 60637, USA.

出版信息

Nat Med. 1996 May;2(5):545-50. doi: 10.1038/nm0596-545.

Abstract

The use of replication-defective adenoviruses (RDAd) for human gene therapy has been limited by host immune responses that result in transient recombinant gene expression in vivo. It remained unclear whether these immune responses were directed predominantly against viral proteins or, alternatively, against foreign transgene-encoded proteins. In this report, we have compared the stability of recombinant gene expression in adult immunocompetent mice following intramuscular (i.m.) injection with identical RDAd encoding self (murine) or foreign (human) erythropoietin. Our results demonstrate that immune responses direct against foreign transgene-encoded proteins are the major determinants of the stability of gene expression following i.m. injection of RDAd. Moreover, we demonstrate long-term recombinant gene expression in immunocompetent animals following a single i.m. injection of RDAd encoding a self protein. These findings are important for the design of future preclinical and clinical gene therapy trials.

摘要

复制缺陷型腺病毒(RDAd)用于人类基因治疗时,会受到宿主免疫反应的限制,导致体内重组基因表达短暂。目前尚不清楚这些免疫反应主要是针对病毒蛋白,还是针对外源转基因编码的蛋白。在本报告中,我们比较了成年免疫活性小鼠肌肉注射相同的编码自身(小鼠)或外源(人类)促红细胞生成素的RDAd后,重组基因表达的稳定性。我们的结果表明,针对外源转基因编码蛋白的免疫反应是肌肉注射RDAd后基因表达稳定性的主要决定因素。此外,我们还证明了在免疫活性动物单次肌肉注射编码自身蛋白的RDAd后,可实现重组基因的长期表达。这些发现对于未来临床前和临床基因治疗试验的设计具有重要意义。

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