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使用重组腺病毒载体将基因转移至脑和脊髓。

Gene transfer to brain and spinal cord using recombinant adenoviral vectors.

作者信息

Alisky Joseph M, Davidson Beverly L

机构信息

Marshfield Clinic Research Foundation, Marshfield, WI, USA.

出版信息

Methods Mol Biol. 2004;246:91-120. doi: 10.1385/1-59259-650-9:91.

DOI:10.1385/1-59259-650-9:91
PMID:14970587
Abstract

Recombinant adenoviral (Ad) vectors are derived from human adenoviruses: nonenveloped, encapsidated linear, double-stranded DNA viruses that commonly cause respiratory and gastrointestinal infections. Forty-three different human adenovirus serotypes have been characterized. Details about production of recombinant Ad vectors are given in Chapter 1. Ad vectors in widespread use are derived from human Ad serotypes 2 and 5 (Ad2 and Ad5), Ad5 being more common for applications in the central nervous system (CNS). Ad5 replication-impaired vectors most often contain deletions in the E1 and E3 regions, with transgenes driven by a variety of promoters including viral promoters, and those that are neuron-specific (2). Recently fiber-modified and "gutless" Ad vectors, and those based on canine adenovirus serotype 2, have been developed for use in brain (3-9).

摘要

重组腺病毒(Ad)载体源自人类腺病毒:无包膜、衣壳化的线性双链DNA病毒,通常引起呼吸道和胃肠道感染。已鉴定出43种不同的人类腺病毒血清型。第1章给出了重组Ad载体生产的详细信息。广泛使用的Ad载体源自人类Ad血清型2和5(Ad2和Ad5),Ad5在中枢神经系统(CNS)应用中更为常见。Ad5复制缺陷型载体最常包含E1和E3区域的缺失,转基因由多种启动子驱动,包括病毒启动子和神经元特异性启动子(2)。最近,已开发出纤维修饰的“无内脏”Ad载体以及基于犬腺病毒血清型2的载体用于脑部(3 - 9)。

相似文献

1
Gene transfer to brain and spinal cord using recombinant adenoviral vectors.使用重组腺病毒载体将基因转移至脑和脊髓。
Methods Mol Biol. 2004;246:91-120. doi: 10.1385/1-59259-650-9:91.
2
Circumvention of anti-adenovirus neutralizing immunity by administration of an adenoviral vector of an alternate serotype.通过给予不同血清型的腺病毒载体规避抗腺病毒中和免疫。
Hum Gene Ther. 1997 Jan 1;8(1):99-109. doi: 10.1089/hum.1997.8.1-99.
3
Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons.辅助依赖型腺病毒载体的给药及不同载体血清型的序贯递送用于狒狒的长期肝靶向基因转移
Proc Natl Acad Sci U S A. 1999 Oct 26;96(22):12816-21. doi: 10.1073/pnas.96.22.12816.
4
Development of oncolytic and gene therapy vectors based on adenovirus serotype 4 as an alternative to adenovirus serotype 5.基于腺病毒血清型 4 的溶瘤和基因治疗载体的开发,作为腺病毒血清型 5 的替代物。
J Gene Med. 2024 Jan;26(1):e3576. doi: 10.1002/jgm.3576. Epub 2023 Aug 14.
5
New serotypes of adenoviral vectors.腺病毒载体的新型血清型
Curr Opin Mol Ther. 2006 Oct;8(5):423-31.
6
Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration.使用不同血清型的辅助依赖型腺病毒载体可允许重复给予载体。
Gene Ther. 1999 Sep;6(9):1565-73. doi: 10.1038/sj.gt.3300995.
7
Targeted adenoviral vectors.靶向腺病毒载体
Biochim Biophys Acta. 2002 May 3;1575(1-3):1-14. doi: 10.1016/s0167-4781(02)00249-x.
8
Fiber-chimeric adenoviruses expressing fibers from serotype 16 and 50 improve gene transfer to human pancreatic adenocarcinoma.表达16型和50型纤维的纤维嵌合腺病毒可改善对人胰腺腺癌的基因转移。
Cancer Gene Ther. 2009 Jul;16(7):585-97. doi: 10.1038/cgt.2009.4. Epub 2009 Jan 30.
9
Adenoviral nerve growth factor and beta-galactosidase transfer to spinal cord: a behavioral and histological analysis.腺病毒介导的神经生长因子和β-半乳糖苷酶向脊髓的转移:行为学和组织学分析。
J Neurosurg. 1999 Jan;90(1 Suppl):99-108. doi: 10.3171/spi.1999.90.1.0099.
10
High-capacity 'gutless' adenoviral vectors.高容量“无内脏”腺病毒载体
Curr Opin Mol Ther. 2001 Oct;3(5):454-63.

引用本文的文献

1
The assessment of adeno-associated vectors as potential intrinsic treatments for brainstem axon regeneration.腺相关病毒作为潜在的脑干轴突再生内在治疗方法的评估。
J Gene Med. 2012 Jan;14(1):20-34. doi: 10.1002/jgm.1628.
2
Adenoviral-mediated modulation of Sim1 expression in the paraventricular nucleus affects food intake.腺病毒介导的室旁核中Sim1表达的调节影响食物摄入。
J Neurosci. 2006 Jun 28;26(26):7116-20. doi: 10.1523/JNEUROSCI.0672-06.2006.