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本文引用的文献

1
Interferon response and viral evasion by members of the family rhabdoviridae.弹状病毒科成员的干扰素反应和病毒逃逸。
Viruses. 2009 Dec;1(3):832-51. doi: 10.3390/v1030832. Epub 2009 Nov 9.
2
Monosynaptic circuit tracing in vivo through Cre-dependent targeting and complementation of modified rabies virus.通过 Cre 依赖性靶向和修饰后的狂犬病毒的互补作用进行体内单突触回路示踪。
Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21848-53. doi: 10.1073/pnas.1011756107. Epub 2010 Nov 29.
3
Rabies virus expressing dendritic cell-activating molecules enhances the innate and adaptive immune response to vaccination.表达树突状细胞激活分子的狂犬病病毒增强了疫苗接种的先天和适应性免疫反应。
J Virol. 2011 Feb;85(4):1634-44. doi: 10.1128/JVI.01552-10. Epub 2010 Nov 24.
4
Rabies virus (RV) glycoprotein expression levels are not critical for pathogenicity of RV.狂犬病病毒 (RV) 糖蛋白的表达水平对于 RV 的致病性并不关键。
J Virol. 2011 Jan;85(2):697-704. doi: 10.1128/JVI.01309-10. Epub 2010 Nov 10.
5
Monosynaptic rabies virus reveals premotor network organization and synaptic specificity of cholinergic partition cells.单突触狂犬病病毒揭示了胆碱能隔区细胞的运动前网络组织和突触特异性。
Neuron. 2010 Nov 4;68(3):456-72. doi: 10.1016/j.neuron.2010.10.019.
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Experimental rabies vaccines for humans.人用狂犬病实验疫苗。
Expert Rev Vaccines. 2010 Oct;9(10):1177-86. doi: 10.1586/erv.10.105.
7
Ascending multisynaptic pathways from the trigeminal ganglion to the anterior cingulate cortex.三叉神经节至前扣带回皮层的上行多突触通路。
Exp Neurol. 2011 Jan;227(1):69-78. doi: 10.1016/j.expneurol.2010.09.013. Epub 2010 Sep 18.
8
Dendritic cells infected by recombinant rabies virus vaccine vector expressing HIV-1 Gag are immunogenic even in the presence of vector-specific immunity.表达 HIV-1 Gag 的重组狂犬病病毒疫苗载体感染的树突状细胞具有免疫原性,即使存在载体特异性免疫。
Vaccine. 2010 Dec 10;29(1):130-40. doi: 10.1016/j.vaccine.2010.08.042. Epub 2010 Aug 20.
9
Generation of recombinant European bat lyssavirus type 1 and inter-genotypic compatibility of lyssavirus genotype 1 and 5 antigenome promoters.重组欧洲蝙蝠 1 型 lyssavirus 的生成和 lyssavirus 基因型 1 和 5 基因组启动子的种间兼容性。
Arch Virol. 2010 Oct;155(10):1631-41. doi: 10.1007/s00705-010-0743-8. Epub 2010 Jul 8.
10
Expression of MIP-1alpha (CCL3) by a recombinant rabies virus enhances its immunogenicity by inducing innate immunity and recruiting dendritic cells and B cells.重组狂犬病病毒表达的 MIP-1alpha(CCL3)通过诱导先天免疫和募集树突状细胞和 B 细胞增强其免疫原性。
J Virol. 2010 Sep;84(18):9642-8. doi: 10.1128/JVI.00326-10. Epub 2010 Jun 30.

狂犬病病毒作为研究工具和病毒疫苗载体。

Rabies virus as a research tool and viral vaccine vector.

机构信息

Department of Microbiology and Immunology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.

出版信息

Adv Virus Res. 2011;79:139-64. doi: 10.1016/B978-0-12-387040-7.00009-3.

DOI:10.1016/B978-0-12-387040-7.00009-3
PMID:21601047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7150175/
Abstract

Until recently, single-stranded negative sense RNA viruses (ssNSVs) were one of only a few important human viral pathogens, which could not be created from cDNA. The inability to manipulate their genomes hindered their detailed genetic analysis. A key paper from Conzelmann's laboratory in 1994 changed this with the publication of a method to recover rabies virus (RABV) from cDNA. This discovery not only dramatically changed the broader field of ssNSV biology but also opened a whole new avenue for studying RABV pathogenicity, developing novel RABV vaccines as well a new generation of RABV-based vaccine vectors, and creating research tools important in neuroscience such as neuronal tracing.

摘要

直到最近,单链负义 RNA 病毒 (ssNSVs) 还是少数几种重要的人类病毒病原体之一,它们不能从 cDNA 中产生。无法操纵它们的基因组阻碍了对其遗传的详细分析。1994 年,Conzelmann 实验室的一篇重要论文发表,该文公布了一种从 cDNA 中回收狂犬病病毒 (RABV) 的方法,改变了这一状况。这一发现不仅极大地改变了 ssNSV 生物学的更广泛领域,也为研究 RABV 的致病性、开发新型 RABV 疫苗和新一代基于 RABV 的疫苗载体开辟了全新的途径,并为神经科学中的研究工具(如神经元示踪)创造了重要条件。