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1
Virus-like particle vaccines containing F or F and G proteins confer protection against respiratory syncytial virus without pulmonary inflammation in cotton rats.含有F蛋白或F蛋白与G蛋白的病毒样颗粒疫苗可使棉鼠免受呼吸道合胞病毒感染,且不会引发肺部炎症。
Hum Vaccin Immunother. 2017 May 4;13(5):1031-1039. doi: 10.1080/21645515.2016.1272743. Epub 2017 Jan 27.
2
Combined virus-like particle and fusion protein-encoding DNA vaccination of cotton rats induces protection against respiratory syncytial virus without causing vaccine-enhanced disease.联合病毒样颗粒和编码融合蛋白的DNA疫苗接种棉鼠可诱导对呼吸道合胞病毒的保护作用,且不会引起疫苗增强性疾病。
Virology. 2016 Jul;494:215-24. doi: 10.1016/j.virol.2016.04.014. Epub 2016 Apr 26.
3
Virus-Like Particle Vaccine Containing the F Protein of Respiratory Syncytial Virus Confers Protection without Pulmonary Disease by Modulating Specific Subsets of Dendritic Cells and Effector T Cells.含有呼吸道合胞病毒F蛋白的病毒样颗粒疫苗通过调节树突状细胞和效应T细胞的特定亚群提供无肺部疾病的保护。
J Virol. 2015 Nov;89(22):11692-705. doi: 10.1128/JVI.02018-15. Epub 2015 Sep 9.
4
Soluble F proteins exacerbate pulmonary histopathology after vaccination upon respiratory syncytial virus challenge but not when presented on virus-like particles.可溶性 F 蛋白在呼吸道合胞病毒攻击后加重疫苗接种后的肺部组织病理学,但在病毒样颗粒上呈现时则不会。
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A Single-Dose Recombinant Parainfluenza Virus 5-Vectored Vaccine Expressing Respiratory Syncytial Virus (RSV) F or G Protein Protected Cotton Rats and African Green Monkeys from RSV Challenge.一种表达呼吸道合胞病毒(RSV)F或G蛋白的单剂量重组副流感病毒5载体疫苗可保护棉鼠和非洲绿猴免受RSV攻击。
J Virol. 2017 May 12;91(11). doi: 10.1128/JVI.00066-17. Print 2017 Jun 1.
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Novel Respiratory Syncytial Virus-Like Particle Vaccine Composed of the Postfusion and Prefusion Conformations of the F Glycoprotein.由F糖蛋白的融合后和融合前构象组成的新型呼吸道合胞病毒样颗粒疫苗。
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Characterization of Epitope-Specific Anti-Respiratory Syncytial Virus (Anti-RSV) Antibody Responses after Natural Infection and after Vaccination with Formalin-Inactivated RSV.自然感染及用福尔马林灭活呼吸道合胞病毒(RSV)疫苗接种后表位特异性抗呼吸道合胞病毒(抗RSV)抗体反应的特征分析
J Virol. 2016 Jun 10;90(13):5965-5977. doi: 10.1128/JVI.00235-16. Print 2016 Jul 1.
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Efficacy of a respiratory syncytial virus vaccine candidate in a maternal immunization model.一种呼吸道合胞病毒候选疫苗在母体免疫模型中的功效。
Nat Commun. 2018 May 15;9(1):1904. doi: 10.1038/s41467-018-04216-6.
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A single intranasal administration of virus-like particle vaccine induces an efficient protection for mice against human respiratory syncytial virus.单次鼻腔内给予病毒样颗粒疫苗可有效保护小鼠免受人类呼吸道合胞病毒感染。
Antiviral Res. 2017 Aug;144:57-69. doi: 10.1016/j.antiviral.2017.05.005. Epub 2017 May 18.

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2
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Natural killer cells contribute to enhanced respiratory disease after oil-in-water emulsion adjuvanted vaccination against respiratory syncytial virus and infection.自然杀伤细胞有助于增强水包油乳剂佐剂疫苗接种呼吸道合胞病毒和感染后的呼吸道疾病。
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Curr Top Microbiol Immunol. 2021;433:77-106. doi: 10.1007/82_2021_232.
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Recombinant Live Attenuated Influenza Virus Expressing Conserved G-Protein Domain in a Chimeric Hemagglutinin Molecule Induces G-Specific Antibodies and Confers Protection against Respiratory Syncytial Virus.在嵌合血凝素分子中表达保守G蛋白结构域的重组减毒活流感病毒可诱导产生G特异性抗体并赋予对呼吸道合胞病毒的保护作用。
Vaccines (Basel). 2020 Dec 1;8(4):716. doi: 10.3390/vaccines8040716.
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Adjuvant effects of killed Lactobacillus casei DK128 on enhancing T helper type 1 immune responses and the efficacy of influenza vaccination in normal and CD4-deficient mice.干酪乳杆菌 DK128 对增强 T 辅助细胞 1 型免疫应答和流感疫苗效果的辅助作用在正常和 CD4 缺陷小鼠中的研究
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Progress in the development of virus-like particle vaccines against respiratory viruses.抗呼吸道病毒的病毒样颗粒疫苗的研发进展。
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本文引用的文献

1
Combined virus-like particle and fusion protein-encoding DNA vaccination of cotton rats induces protection against respiratory syncytial virus without causing vaccine-enhanced disease.联合病毒样颗粒和编码融合蛋白的DNA疫苗接种棉鼠可诱导对呼吸道合胞病毒的保护作用,且不会引起疫苗增强性疾病。
Virology. 2016 Jul;494:215-24. doi: 10.1016/j.virol.2016.04.014. Epub 2016 Apr 26.
2
Cotton rat immune responses to virus-like particles containing the pre-fusion form of respiratory syncytial virus fusion protein.棉鼠对含有呼吸道合胞病毒融合蛋白前融合形式的病毒样颗粒的免疫反应。
J Transl Med. 2015 Nov 5;13:350. doi: 10.1186/s12967-015-0705-8.
3
Virus-Like Particle Vaccine Containing the F Protein of Respiratory Syncytial Virus Confers Protection without Pulmonary Disease by Modulating Specific Subsets of Dendritic Cells and Effector T Cells.含有呼吸道合胞病毒F蛋白的病毒样颗粒疫苗通过调节树突状细胞和效应T细胞的特定亚群提供无肺部疾病的保护。
J Virol. 2015 Nov;89(22):11692-705. doi: 10.1128/JVI.02018-15. Epub 2015 Sep 9.
4
A Randomized, Blinded, Controlled, Dose-Ranging Study of a Respiratory Syncytial Virus Recombinant Fusion (F) Nanoparticle Vaccine in Healthy Women of Childbearing Age.一项在健康育龄期女性中进行的呼吸道合胞病毒重组融合(F)纳米颗粒疫苗的随机、双盲、对照、剂量范围研究。
J Infect Dis. 2016 Feb 1;213(3):411-22. doi: 10.1093/infdis/jiv406. Epub 2015 Aug 10.
5
Additive protection induced by mixed virus-like particles presenting respiratory syncytial virus fusion or attachment glycoproteins.呈现呼吸道合胞病毒融合或附着糖蛋白的混合病毒样颗粒诱导的附加保护作用。
Antiviral Res. 2014 Nov;111:129-35. doi: 10.1016/j.antiviral.2014.09.005. Epub 2014 Sep 18.
6
Co-immunization with virus-like particle and DNA vaccines induces protection against respiratory syncytial virus infection and bronchiolitis.病毒样颗粒与DNA疫苗联合免疫可诱导对呼吸道合胞病毒感染和细支气管炎的保护作用。
Antiviral Res. 2014 Oct;110:115-23. doi: 10.1016/j.antiviral.2014.07.016. Epub 2014 Aug 7.
7
Modification of the respiratory syncytial virus f protein in virus-like particles impacts generation of B cell memory.呼吸道合胞病毒F蛋白在病毒样颗粒中的修饰影响B细胞记忆的产生。
J Virol. 2014 Sep 1;88(17):10165-76. doi: 10.1128/JVI.01250-14. Epub 2014 Jun 25.
8
Safety and immunogenicity of a Sf9 insect cell-derived respiratory syncytial virus fusion protein nanoparticle vaccine.Sf9 昆虫细胞来源的呼吸道合胞病毒融合蛋白纳米颗粒疫苗的安全性和免疫原性。
Vaccine. 2013 Jan 7;31(3):524-32. doi: 10.1016/j.vaccine.2012.11.009. Epub 2012 Nov 12.
9
A stabilized respiratory syncytial virus reverse genetics system amenable to recombination-mediated mutagenesis.一种稳定的呼吸道合胞病毒反向遗传学系统,适用于重组介导的诱变。
Virology. 2012 Dec 5;434(1):129-36. doi: 10.1016/j.virol.2012.09.022. Epub 2012 Oct 11.
10
Long-term and memory immune responses in mice against Newcastle disease virus-like particles containing respiratory syncytial virus glycoprotein ectodomains.含呼吸道合胞病毒糖蛋白胞外域的新城疫病毒样颗粒在小鼠体内的长期和记忆免疫应答。
J Virol. 2012 Nov;86(21):11654-62. doi: 10.1128/JVI.01510-12. Epub 2012 Aug 15.

含有F蛋白或F蛋白与G蛋白的病毒样颗粒疫苗可使棉鼠免受呼吸道合胞病毒感染,且不会引发肺部炎症。

Virus-like particle vaccines containing F or F and G proteins confer protection against respiratory syncytial virus without pulmonary inflammation in cotton rats.

作者信息

Hwang Hye Suk, Kim Ki-Hye, Lee Youri, Lee Young-Tae, Ko Eun-Ju, Park SooJin, Lee Jong Seok, Lee Byung-Cheol, Kwon Young-Man, Moore Martin L, Kang Sang-Moo

机构信息

a Center for Inflammation, Immunity & Infection , Institute for Biomedical Sciences, Georgia State University , Atlanta , GA , USA.

b National Institute of Biological Resources , Incheon , South Korea.

出版信息

Hum Vaccin Immunother. 2017 May 4;13(5):1031-1039. doi: 10.1080/21645515.2016.1272743. Epub 2017 Jan 27.

DOI:10.1080/21645515.2016.1272743
PMID:28129031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5443399/
Abstract

Vaccine-enhanced disease has been a major obstacle in developing a safe vaccine against respiratory syncytial virus (RSV). This study demonstrates the immunogenicity, efficacy, and safety of virus-like particle (VLP) vaccines containing RSV F (F VLP), G (G VLP), or F and G proteins (FG VLP) in cotton rats. RSV specific antibodies were effectively induced by vaccination of cotton rats with F VLP or FG VLP vaccines. After challenge, lung RSV clearance was observed with RSV F, G, FG VLP, and formalin inactivated RSV (FI-RSV) vaccines. Upon RSV infection, cotton rats with RSV VLP vaccines were protected against airway hyper-responsiveness and weight loss, which are different from FI-RSV vaccination exhibiting vaccine-enhanced disease of airway obstruction, weight loss, and severe histopathology with eosinophilia and mucus production. FG VLP and F VLP vaccines did not cause pulmonary inflammation whereas G VLP induced moderate lung inflammation with eosinophilia and mucus production. In particular, F VLP and FG VLP vaccines were found to be effective in inducing antibody secreting cell responses in bone marrow and lymphoid organs as well as avoiding the induction of T helper type 2 cytokines. These results provide further evidence to develop a safe RSV vaccine based on VLP platforms.

摘要

疫苗增强型疾病一直是开发安全的呼吸道合胞病毒(RSV)疫苗的主要障碍。本研究证明了含RSV F(F VLP)、G(G VLP)或F和G蛋白(FG VLP)的病毒样颗粒(VLP)疫苗在棉鼠中的免疫原性、有效性和安全性。用F VLP或FG VLP疫苗接种棉鼠可有效诱导RSV特异性抗体。攻毒后,RSV F、G、FG VLP和福尔马林灭活RSV(FI-RSV)疫苗均观察到肺内RSV清除。RSV感染后,接种RSV VLP疫苗的棉鼠可免受气道高反应性和体重减轻的影响,这与接种FI-RSV疫苗后出现的疫苗增强型疾病不同,后者表现为气道阻塞、体重减轻以及伴有嗜酸性粒细胞增多和黏液产生的严重组织病理学变化。FG VLP和F VLP疫苗未引起肺部炎症,而G VLP诱导了伴有嗜酸性粒细胞增多和黏液产生的中度肺部炎症。特别是,发现F VLP和FG VLP疫苗可有效诱导骨髓和淋巴器官中的抗体分泌细胞反应,并避免诱导2型辅助性T细胞细胞因子。这些结果为基于VLP平台开发安全的RSV疫苗提供了进一步的证据。