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病毒感染的识别和非包膜病毒载体的早期先天反应。

Virus infection recognition and early innate responses to non-enveloped viral vectors.

机构信息

Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195-7720, USA.

出版信息

Viruses. 2010 Jan;2(1):244-261. doi: 10.3390/v2010244. Epub 2010 Jan 19.

DOI:10.3390/v2010244
PMID:21994609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3185565/
Abstract

Numerous human genetic and acquired diseases could be corrected or ameliorated if viruses are harnessed to safely and effectively deliver therapeutic genes to diseased cells and tissues in vivo. Innate immune and inflammatory response represents one of the key stumbling blocks during the development of viral-based therapies. In this review, current data on the early innate immune responses to viruses and to the most commonly used gene therapy vectors (using adenovirus and adeno-associated virus) will be discussed. Recent findings in the field may help develop new approaches to moderate these innate immune anti-viral responses and thus improve the safety of viral vectors for human gene therapy applications.

摘要

如果能够利用病毒将治疗基因安全有效地递送到体内患病细胞和组织中,许多人类遗传性和获得性疾病都可以得到纠正或改善。先天免疫和炎症反应是病毒治疗发展过程中的关键障碍之一。在这篇综述中,将讨论目前关于病毒和最常用的基因治疗载体(使用腺病毒和腺相关病毒)的早期先天免疫反应的相关数据。该领域的最新发现可能有助于开发新方法来调节这些先天免疫抗病毒反应,从而提高病毒载体用于人类基因治疗应用的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98b5/3185565/4ce5ebb6dc86/viruses-02-00244f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98b5/3185565/4ce5ebb6dc86/viruses-02-00244f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98b5/3185565/4ce5ebb6dc86/viruses-02-00244f1.jpg

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J Clin Invest. 2009 Aug;119(8):2388-98. doi: 10.1172/JCI37607. Epub 2009 Jul 1.
2
Virus binding to a plasma membrane receptor triggers interleukin-1 alpha-mediated proinflammatory macrophage response in vivo.病毒与质膜受体的结合在体内触发白细胞介素-1α介导的促炎性巨噬细胞反应。
Immunity. 2009 Jul 17;31(1):110-21. doi: 10.1016/j.immuni.2009.04.015. Epub 2009 Jul 2.
3
5'-triphosphate RNA requires base-paired structures to activate antiviral signaling via RIG-I.
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PLoS One. 2022 May 9;17(5):e0263901. doi: 10.1371/journal.pone.0263901. eCollection 2022.
4
T cell receptor signaling pathway and cytokine-cytokine receptor interaction affect the rehabilitation process after respiratory syncytial virus infection.T细胞受体信号通路和细胞因子-细胞因子受体相互作用影响呼吸道合胞病毒感染后的康复过程。
PeerJ. 2019 Jun 12;7:e7089. doi: 10.7717/peerj.7089. eCollection 2019.
5
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Mol Ther. 2018 Oct 3;26(10):2337-2356. doi: 10.1016/j.ymthe.2018.07.011. Epub 2018 Jul 17.
6
Oncolytic virotherapy for osteosarcoma using midkine promoter-regulated adenoviruses.使用中期因子启动子调控腺病毒的骨肉瘤溶瘤病毒疗法
Cancer Gene Ther. 2014 Mar;21(3):126-32. doi: 10.1038/cgt.2014.7. Epub 2014 Feb 28.
7
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7
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