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本文引用的文献

1
Inhibition of Innate Immune Responses Is Key to Pathogenesis by Arenaviruses.抑制先天免疫反应是沙粒病毒发病机制的关键。
J Virol. 2016 Mar 28;90(8):3810-3818. doi: 10.1128/JVI.03049-15. Print 2016 Apr.
2
A Novel Live Pichinde Virus-Based Vaccine Vector Induces Enhanced Humoral and Cellular Immunity after a Booster Dose.一种新型的基于皮钦德活病毒的疫苗载体在加强剂量后可诱导增强的体液免疫和细胞免疫。
J Virol. 2015 Dec 16;90(5):2551-60. doi: 10.1128/JVI.02705-15.
3
Arenavirus reverse genetics for vaccine development.沙粒病毒反向遗传学在疫苗开发中的应用。
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4
Expanded potential for recombinant trisegmented lymphocytic choriomeningitis viruses: protein production, antibody production, and in vivo assessment of biological function of genes of interest.扩展重组三片段淋巴细胞脉络丛脑膜炎病毒的潜力:目的基因的蛋白生产、抗体生产和体内生物学功能评估。
J Virol. 2011 Aug;85(15):7928-32. doi: 10.1128/JVI.00486-11. Epub 2011 May 25.
5
Development of replication-defective lymphocytic choriomeningitis virus vectors for the induction of potent CD8+ T cell immunity.复制缺陷型淋巴细胞脉络丛脑膜炎病毒载体的构建及其诱导强烈的 CD8+ T 细胞免疫反应的研究。
Nat Med. 2010 Mar;16(3):339-45. doi: 10.1038/nm.2104. Epub 2010 Feb 7.
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The mouse model for influenza.流感小鼠模型。
Curr Protoc Microbiol. 2009 May;Chapter 15:Unit 15G.3. doi: 10.1002/9780471729259.mc15g03s13.
7
Development of infectious clones for virulent and avirulent pichinde viruses: a model virus to study arenavirus-induced hemorrhagic fevers.强毒和无毒皮钦德病毒感染性克隆的构建:一种用于研究沙粒病毒引起的出血热的模型病毒
J Virol. 2009 Jul;83(13):6357-62. doi: 10.1128/JVI.00019-09. Epub 2009 Apr 22.
8
Generation of recombinant lymphocytic choriomeningitis viruses with trisegmented genomes stably expressing two additional genes of interest.具有稳定表达两个额外感兴趣基因的三段式基因组的重组淋巴细胞性脉络丛脑膜炎病毒的产生。
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3473-8. doi: 10.1073/pnas.0900088106. Epub 2009 Feb 10.
9
Pichindé virus, a new virus of the Tacaribe group from Colombia.皮钦德病毒,一种来自哥伦比亚的塔卡里贝病毒群的新型病毒。
Am J Trop Med Hyg. 1971 Jul;20(4):631-41.

重组三段式皮钦德病毒作为一种新型活病毒疫苗平台。

Recombinant Tri-Segmented Pichinde Virus as a Novel Live Viral Vaccine Platform.

作者信息

Dhanwani Rekha, Ly Hinh, Liang Yuying

机构信息

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, 1988 Fitch Ave., Ste 295, Animal Science/Veterinary Medicine Building, Saint Paul, MN, 55108, USA.

La Jolla Institute for Allergy & Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA.

出版信息

Methods Mol Biol. 2017;1581:169-179. doi: 10.1007/978-1-4939-6869-5_10.

DOI:10.1007/978-1-4939-6869-5_10
PMID:28374249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6340294/
Abstract

Pichinde virus (PICV) is a nonpathogenic arenavirus with a bi-segmented RNA genome (L and S segments) that encodes four viral genes. We have developed a reverse genetics system to generate recombinant tri-segmented PICV (rP18tri) that packages three RNA segments (L, S1, and S2) and can encode up to two foreign genes. Using influenza virus HA and NP as model antigens, we show that the rP18tri vector can induce strong humoral and cell-mediated immunity, which further increases upon a booster dose. We propose that this novel rP18tri vector can be developed into a useful vaccine platform for other antigens, particularly when strong cellular immunity and prime-boost vaccination strategy are desired.

摘要

皮钦德病毒(PICV)是一种非致病性沙粒病毒,其RNA基因组由两个片段(L和S片段)组成,编码四种病毒基因。我们开发了一种反向遗传学系统,以产生重组三段式PICV(rP18tri),该病毒包装三个RNA片段(L、S1和S2),最多可编码两个外源基因。以流感病毒HA和NP作为模型抗原,我们发现rP18tri载体可诱导强烈的体液免疫和细胞介导免疫,加强免疫后免疫反应进一步增强。我们认为,这种新型rP18tri载体可开发成为针对其他抗原的有效疫苗平台,特别是在需要强大细胞免疫和初免-加强免疫策略的情况下。