• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

植物源亚单位肺炎鼠疫和腺鼠疫疫苗在小鼠中具有口服免疫原性。

Plant-made subunit vaccine against pneumonic and bubonic plague is orally immunogenic in mice.

作者信息

Alvarez M Lucrecia, Pinyerd Heidi L, Crisantes Jason D, Rigano M Manuela, Pinkhasov Julia, Walmsley Amanda M, Mason Hugh S, Cardineau Guy A

机构信息

Center for Infectious Diseases and Vaccinology (CIDV), The Biodesign Institute at Arizona State University, 1001 South McAllister Avenue, Tempe, AZ 85287-4501, USA.

出版信息

Vaccine. 2006 Mar 24;24(14):2477-90. doi: 10.1016/j.vaccine.2005.12.057. Epub 2006 Jan 13.

DOI:10.1016/j.vaccine.2005.12.057
PMID:16442673
Abstract

Yersinia pestis, the causative agent of plague, is an extremely virulent bacterium but there are no approved vaccines for protection against it. Our goal was to produce a vaccine that would address: ease of delivery, mucosal efficacy, safety, rapid scalability, and cost. We developed a novel production and delivery system for a plague vaccine of a Y. pestis F1-V antigen fusion protein expressed in tomato. Immunogenicity of the F1-V transgenic tomatoes was confirmed in mice that were primed subcutaneously with bacterially-produced F1-V and boosted orally with transgenic tomato fruit. Expression of the plague antigens in fruit allowed producing an oral vaccine candidate without protein purification and with minimal processing technology.

摘要

鼠疫耶尔森菌是鼠疫的病原体,是一种极具毒性的细菌,但目前尚无经批准用于预防鼠疫的疫苗。我们的目标是研发一种疫苗,该疫苗应具备:易于接种、黏膜有效性、安全性、快速可扩展性以及低成本等特性。我们开发了一种新型的生产和接种系统,用于生产在番茄中表达的鼠疫耶尔森菌F1-V抗原融合蛋白的鼠疫疫苗。在先用细菌生产的F1-V进行皮下初免,然后用转基因番茄果实进行口服加强免疫的小鼠中,证实了F1-V转基因番茄的免疫原性。鼠疫抗原在果实中的表达使得无需进行蛋白质纯化且采用最少的加工技术就能生产出一种口服疫苗候选物。

相似文献

1
Plant-made subunit vaccine against pneumonic and bubonic plague is orally immunogenic in mice.植物源亚单位肺炎鼠疫和腺鼠疫疫苗在小鼠中具有口服免疫原性。
Vaccine. 2006 Mar 24;24(14):2477-90. doi: 10.1016/j.vaccine.2005.12.057. Epub 2006 Jan 13.
2
Intranasal delivery of a protein subunit vaccine using a Tobacco Mosaic Virus platform protects against pneumonic plague.使用烟草花叶病毒平台进行鼻内递送蛋白质亚基疫苗可预防肺鼠疫。
Vaccine. 2016 Nov 11;34(47):5768-5776. doi: 10.1016/j.vaccine.2016.09.063. Epub 2016 Oct 13.
3
Prevention of bubonic and pneumonic plague using plant-derived vaccines.植物源疫苗在预防腺鼠疫和肺鼠疫中的应用。
Biotechnol Adv. 2010 Jan-Feb;28(1):184-96. doi: 10.1016/j.biotechadv.2009.11.006.
4
Complete Protection against Pneumonic and Bubonic Plague after a Single Oral Vaccination.单次口服疫苗接种后对肺鼠疫和腺鼠疫的完全防护
PLoS Negl Trop Dis. 2015 Oct 16;9(10):e0004162. doi: 10.1371/journal.pntd.0004162. eCollection 2015.
5
Effective plague vaccination via oral delivery of plant cells expressing F1-V antigens in chloroplasts.通过口服表达叶绿体中F1-V抗原的植物细胞实现有效的鼠疫疫苗接种。
Infect Immun. 2008 Aug;76(8):3640-50. doi: 10.1128/IAI.00050-08. Epub 2008 May 27.
6
Developing subunit immunogens using B and T cell epitopes and their constructs derived from the F1 antigen of Yersinia pestis using novel delivery vehicles.利用新型递送载体,开发使用B细胞和T细胞表位及其源自鼠疫耶尔森氏菌F1抗原构建体的亚单位免疫原。
FEMS Immunol Med Microbiol. 2003 Oct 15;38(3):215-29. doi: 10.1016/S0928-8244(03)00170-6.
7
Expression of an immunogenic F1-V fusion protein in lettuce as a plant-based vaccine against plague.生菜中表达免疫原性 F1-V 融合蛋白作为抗鼠疫植物疫苗。
Planta. 2010 Jul;232(2):409-16. doi: 10.1007/s00425-010-1176-z. Epub 2010 May 12.
8
Recombinant V antigen protects mice against pneumonic and bubonic plague caused by F1-capsule-positive and -negative strains of Yersinia pestis.重组V抗原可保护小鼠免受由鼠疫耶尔森氏菌F1荚膜阳性和阴性菌株引起的肺鼠疫和腺鼠疫。
Infect Immun. 1996 Nov;64(11):4580-5. doi: 10.1128/iai.64.11.4580-4585.1996.
9
Prevention of pneumonic plague in mice, rats, guinea pigs and non-human primates with clinical grade rV10, rV10-2 or F1-V vaccines.用临床级 rV10、rV10-2 或 F1-V 疫苗预防鼠、大鼠、豚鼠和非人类灵长类动物的肺鼠疫。
Vaccine. 2011 Sep 2;29(38):6572-83. doi: 10.1016/j.vaccine.2011.06.119. Epub 2011 Jul 16.
10
Complete Protection Against in BALB/c Mouse Model Elicited by Immunization With Inhalable Formulations of rF1-V10 Fusion Protein Aerosolized Intratracheal Inoculation.通过雾化吸入途径接种 rF1-V10 融合蛋白吸入制剂免疫 BALB/c 小鼠模型诱导产生的 完全保护作用。
Front Immunol. 2022 Jan 26;13:793382. doi: 10.3389/fimmu.2022.793382. eCollection 2022.

引用本文的文献

1
Live Plague Vaccine Development: Past, Present, and Future.鼠疫活疫苗的研发:过去、现在与未来
Vaccines (Basel). 2025 Jan 13;13(1):66. doi: 10.3390/vaccines13010066.
2
Exploring recent progress of molecular farming for therapeutic and recombinant molecules in plant systems.探索植物系统中用于治疗性和重组分子的分子农业的最新进展。
Heliyon. 2024 Sep 7;10(18):e37634. doi: 10.1016/j.heliyon.2024.e37634. eCollection 2024 Sep 30.
3
Immunogenicity and efficacy of recombinant subunit SARS-CoV-2 vaccine candidate in the Syrian hamster model.
重组亚单位SARS-CoV-2候选疫苗在叙利亚仓鼠模型中的免疫原性和疗效
Biotechnol Rep (Amst). 2023 Mar;37:e00779. doi: 10.1016/j.btre.2022.e00779. Epub 2022 Dec 13.
4
Plant Platforms for Efficient Heterologous Protein Production.用于高效异源蛋白生产的植物平台
Biotechnol Bioprocess Eng. 2021;26(4):546-567. doi: 10.1007/s12257-020-0374-1. Epub 2021 Aug 7.
5
Induction of Immune Response in Animal Model Using Recombinant Anti-NDV Vaccine.使用重组抗新城疫病毒疫苗在动物模型中诱导免疫反应
Iran J Biotechnol. 2019 Jan 11;17(1):e2215. doi: 10.21859/ijb.2215. eCollection 2019 Jan.
6
Disease Prevention: An Opportunity to Expand Edible Plant-Based Vaccines?疾病预防:拓展可食用植物性疫苗的契机?
Vaccines (Basel). 2017 May 30;5(2):14. doi: 10.3390/vaccines5020014.
7
A Perspective on the Development of Plant-Made Vaccines in the Fight against Ebola Virus.关于植物源疫苗在抗击埃博拉病毒方面发展的展望
Front Immunol. 2017 Mar 10;8:252. doi: 10.3389/fimmu.2017.00252. eCollection 2017.
8
The Last Ten Years of Advancements in Plant-Derived Recombinant Vaccines against Hepatitis B.植物源重组乙肝疫苗的十年进展
Int J Mol Sci. 2016 Oct 13;17(10):1715. doi: 10.3390/ijms17101715.
9
Plague Vaccines: Status and Future.鼠疫疫苗:现状与未来
Adv Exp Med Biol. 2016;918:313-360. doi: 10.1007/978-94-024-0890-4_12.
10
A Replication-Defective Human Type 5 Adenovirus-Based Trivalent Vaccine Confers Complete Protection against Plague in Mice and Nonhuman Primates.一种基于复制缺陷型人5型腺病毒的三价疫苗可使小鼠和非人灵长类动物获得针对鼠疫的完全保护。
Clin Vaccine Immunol. 2016 Jul 5;23(7):586-600. doi: 10.1128/CVI.00150-16. Print 2016 Jul.