• 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

一种展示口蹄疫病毒中和表位的基于铁蛋白的纳米颗粒在豚鼠中赋予部分保护作用。

A ferritin-based nanoparticle displaying a neutralizing epitope for foot-and-mouth disease virus (FMDV) confers partial protection in guinea pigs.

机构信息

College of Veterinary Medicine, Gansu Agricultural University, Lanzhou, 730070, China.

State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.

出版信息

BMC Vet Res. 2024 Jul 6;20(1):301. doi: 10.1186/s12917-024-04159-9.

DOI:10.1186/s12917-024-04159-9
PMID:38971791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11227194/
Abstract

BACKGROUND

Foot-and-mouth disease (FMD) is a devastating disease affecting cloven-hoofed animals, that leads to significant economic losses in affected countries and regions. Currently, there is an evident inclination towards the utilization of nanoparticles as powerful platforms for innovative vaccine development. Therefore, this study developed a ferritin-based nanoparticle (FNP) vaccine that displays a neutralizing epitope of foot-and-mouth disease virus (FMDV) VP1 (aa 140-158) on the surface of FNP, and evaluated the immunogenicity and protective efficacy of these FNPs in mouse and guinea pig models to provide a strategy for developing potential FMD vaccines.

RESULTS

This study expressed the recombinant proteins Hpf, HPF-NE and HPF-T34E via an E. coli expression system. The results showed that the recombinant proteins Hpf, Hpf-NE and Hpf-T34E could be effectively assembled into nanoparticles. Subsequently, we evaluated the immunogenicity of the Hpf, Hpf-NE and Hpf-T34E proteins in mice, as well as the immunogenicity and protectiveness of the Hpf-T34E protein in guinea pigs. The results of the mouse experiment showed that the immune efficacy in the Hpf-T34E group was greater than the Hpf-NE group. The results from guinea pigs immunized with Hpf-T34E showed that the immune efficacy was largely consistent with the immunogenicity of the FMD inactivated vaccine (IV) and could confer partial protection against FMDV challenge in guinea pigs.

CONCLUSIONS

The Hpf-T34E nanoparticles stand out as a superior choice for a subunit vaccine candidate against FMD, offering effective protection in FMDV-infected model animals. FNP-based vaccines exhibit excellent safety and immunogenicity, thus representing a promising strategy for the continued development of highly efficient and safe FMD vaccines.

摘要

背景

口蹄疫(FMD)是一种严重影响偶蹄动物的疾病,会给受影响的国家和地区带来重大经济损失。目前,纳米粒子作为创新疫苗开发的强大平台的应用趋势明显。因此,本研究开发了一种基于铁蛋白的纳米颗粒(FNP)疫苗,该疫苗在 FNP 表面展示了口蹄疫病毒(FMDV)VP1(aa 140-158)的中和表位,评估了这些 FNPs 在小鼠和豚鼠模型中的免疫原性和保护效力,为开发潜在的 FMD 疫苗提供了一种策略。

结果

本研究通过大肠杆菌表达系统表达了重组蛋白 Hpf、HPF-NE 和 HPF-T34E。结果表明,重组蛋白 Hpf、Hpf-NE 和 Hpf-T34E 可以有效地组装成纳米颗粒。随后,我们评估了 Hpf、Hpf-NE 和 Hpf-T34E 蛋白在小鼠中的免疫原性,以及 Hpf-T34E 蛋白在豚鼠中的免疫原性和保护效力。小鼠实验结果表明,Hpf-T34E 组的免疫效果大于 Hpf-NE 组。用 Hpf-T34E 免疫的豚鼠的结果表明,免疫效果与口蹄疫灭活疫苗(IV)的免疫原性基本一致,可对豚鼠的 FMDV 攻毒提供部分保护。

结论

Hpf-T34E 纳米颗粒作为 FMD 亚单位疫苗候选物具有优势,可有效保护 FMDV 感染的模型动物。基于 FNP 的疫苗具有良好的安全性和免疫原性,因此代表了继续开发高效、安全的 FMD 疫苗的有前途的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/60aed7bd7d4d/12917_2024_4159_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/d3c0f6ad797d/12917_2024_4159_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/c65126201a67/12917_2024_4159_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/e549aef9f813/12917_2024_4159_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/6b2a944dcb92/12917_2024_4159_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/60aed7bd7d4d/12917_2024_4159_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/d3c0f6ad797d/12917_2024_4159_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/c65126201a67/12917_2024_4159_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/e549aef9f813/12917_2024_4159_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/6b2a944dcb92/12917_2024_4159_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ead/11227194/60aed7bd7d4d/12917_2024_4159_Fig5_HTML.jpg

相似文献

1
A ferritin-based nanoparticle displaying a neutralizing epitope for foot-and-mouth disease virus (FMDV) confers partial protection in guinea pigs.一种展示口蹄疫病毒中和表位的基于铁蛋白的纳米颗粒在豚鼠中赋予部分保护作用。
BMC Vet Res. 2024 Jul 6;20(1):301. doi: 10.1186/s12917-024-04159-9.
2
Immunogenicity of T7 bacteriophage nanoparticles displaying G-H loop of foot-and-mouth disease virus (FMDV).展示口蹄疫病毒(FMDV)G-H环的T7噬菌体纳米颗粒的免疫原性
Vet Microbiol. 2017 Jun;205:46-52. doi: 10.1016/j.vetmic.2017.04.023. Epub 2017 May 4.
3
Immune responses of recombinant adenovirus co-expressing VP1 of foot-and-mouth disease virus and porcine interferon alpha in mice and guinea pigs.共表达口蹄疫病毒VP1和猪α干扰素的重组腺病毒在小鼠和豚鼠体内的免疫反应
Vet Immunol Immunopathol. 2008 Aug 15;124(3-4):274-83. doi: 10.1016/j.vetimm.2008.04.011. Epub 2008 Apr 22.
4
A Heat-Induced Mutation on VP1 of Foot-and-Mouth Disease Virus Serotype O Enhanced Capsid Stability and Immunogenicity.口蹄疫病毒 O 型 VP1 热诱导突变增强了衣壳稳定性和免疫原性。
J Virol. 2021 Jul 26;95(16):e0017721. doi: 10.1128/JVI.00177-21.
5
Foot-and-mouth disease virus-like particles produced by a SUMO fusion protein system in Escherichia coli induce potent protective immune responses in guinea pigs, swine and cattle.大肠杆菌中 SUMO 融合蛋白系统产生的口蹄疫病毒样颗粒在豚鼠、猪和牛中诱导强烈的保护性免疫应答。
Vet Res. 2013 Jul 4;44(1):48. doi: 10.1186/1297-9716-44-48.
6
A ferritin nanoparticle vaccine for foot-and-mouth disease virus elicited partial protection in mice.口蹄疫病毒铁蛋白纳米颗粒疫苗在小鼠中引发部分保护。
Vaccine. 2020 Jul 31;38(35):5647-5652. doi: 10.1016/j.vaccine.2020.06.063. Epub 2020 Jul 3.
7
Immunogenicity and protective efficacy of recombinant proteins consisting of multiple epitopes of foot-and-mouth disease virus fused with flagellin.融合了口蹄疫病毒多个表位的鞭毛蛋白的重组蛋白的免疫原性和保护效力。
Appl Microbiol Biotechnol. 2019 Apr;103(8):3367-3379. doi: 10.1007/s00253-019-09691-5. Epub 2019 Mar 19.
8
Sindbis virus replicase-based DNA vaccine construct encoding FMDV-specific multivalent epitope gene: studies on its immune responses in guinea pigs.基于辛德毕斯病毒复制酶的 DNA 疫苗构建体,编码口蹄疫病毒特异性多价表位基因:在豚鼠中的免疫应答研究。
Scand J Immunol. 2012 Oct;76(4):345-53. doi: 10.1111/j.1365-3083.2012.02733.x.
9
Enhanced immunogenicity of multiple-epitopes of foot-and-mouth disease virus fused with porcine interferon alpha in mice and protective efficacy in guinea pigs and swine.口蹄疫病毒多表位与猪α干扰素融合物在小鼠中的免疫原性增强及在豚鼠和猪中的保护效果
J Virol Methods. 2008 Apr;149(1):144-52. doi: 10.1016/j.jviromet.2007.12.018. Epub 2008 Feb 21.
10
BacMam Expressing Highly Glycosylated Porcine Interferon Alpha Induces Robust Antiviral and Adjuvant Effects against Foot-and-Mouth Disease Virus in Pigs.BacMam 表达的高度糖基化猪干扰素 α 可在猪中诱导针对口蹄疫病毒的强大抗病毒和佐剂作用。
J Virol. 2022 Jun 22;96(12):e0052822. doi: 10.1128/jvi.00528-22. Epub 2022 May 23.

引用本文的文献

1
Preparation and Immunogenicity Evaluation of a Ferritin-Based GnRH Nanoparticle Vaccine.基于铁蛋白的促性腺激素释放激素纳米颗粒疫苗的制备及免疫原性评估
Vaccines (Basel). 2025 Jul 23;13(8):781. doi: 10.3390/vaccines13080781.
2
A meta-analysis on the effectiveness of serotype O foot-and-mouth disease vaccines.O型口蹄疫疫苗有效性的荟萃分析。
Sci Rep. 2025 May 2;15(1):15381. doi: 10.1038/s41598-025-99518-3.
3
Self-Assembled Ferritin Nanoparticles for Delivery of Antigens and Development of Vaccines: From Structure and Property to Applications.

本文引用的文献

1
Editorial: Foot-and-mouth disease epidemiology, vaccines and vaccination: moving forward.社论:口蹄疫流行病学、疫苗与接种:迈向未来
Front Vet Sci. 2023 Jun 20;10:1231005. doi: 10.3389/fvets.2023.1231005. eCollection 2023.
2
A Ferritin Nanoparticle-Based Zika Virus Vaccine Candidate Induces Robust Humoral and Cellular Immune Responses and Protects Mice from Lethal Virus Challenge.一种基于铁蛋白纳米颗粒的寨卡病毒候选疫苗可诱导强烈的体液免疫和细胞免疫反应,并保护小鼠免受致命病毒攻击。
Vaccines (Basel). 2023 Apr 10;11(4):821. doi: 10.3390/vaccines11040821.
3
A ferritin-based COVID-19 nanoparticle vaccine that elicits robust, durable, broad-spectrum neutralizing antisera in non-human primates.
自组装铁蛋白纳米颗粒用于抗原传递和疫苗开发:从结构和性质到应用。
Molecules. 2024 Sep 5;29(17):4221. doi: 10.3390/molecules29174221.
一种基于铁蛋白的 COVID-19 纳米颗粒疫苗,在非人类灵长类动物中引发了强大、持久、广谱的中和抗体血清。
Nat Commun. 2023 Apr 17;14(1):2149. doi: 10.1038/s41467-023-37417-9.
4
Development of Foot-and-Mouth Disease Vaccines in Recent Years.近年来口蹄疫疫苗的发展
Vaccines (Basel). 2022 Oct 28;10(11):1817. doi: 10.3390/vaccines10111817.
5
Self-Assembling Protein Nanoparticles in the Design of Vaccines: 2022 Update.疫苗设计中的自组装蛋白纳米颗粒:2022年更新
Vaccines (Basel). 2022 Sep 2;10(9):1447. doi: 10.3390/vaccines10091447.
6
Self-Assembling Nanovaccine Confers Complete Protection Against Zika Virus Without Causing Antibody-Dependent Enhancement.自组装纳米疫苗可提供针对寨卡病毒的完全保护,而不会引起抗体依赖性增强作用。
Front Immunol. 2022 May 9;13:905431. doi: 10.3389/fimmu.2022.905431. eCollection 2022.
7
Generation of Replication Deficient Human Adenovirus 5 (Ad5) Vectored FMD Vaccines.复制缺陷型人 5 型腺病毒(Ad5)载体口蹄疫疫苗的研制。
Methods Mol Biol. 2022;2465:155-175. doi: 10.1007/978-1-0716-2168-4_9.
8
Elicitation of Neutralizing Antibody Responses to HIV-1 Immunization with Nanoparticle Vaccine Platforms.纳米颗粒疫苗平台诱导 HIV-1 免疫的中和抗体反应。
Viruses. 2021 Jul 2;13(7):1296. doi: 10.3390/v13071296.
9
Chimeric RHDV Virus-Like Particles Displaying Foot-and-Mouth Disease Virus Epitopes Elicit Neutralizing Antibodies and Confer Partial Protection in Pigs.展示口蹄疫病毒表位的嵌合兔出血症病毒样颗粒可诱导中和抗体并在猪中提供部分保护。
Vaccines (Basel). 2021 May 7;9(5):470. doi: 10.3390/vaccines9050470.
10
Multivalent Display of SARS-CoV-2 Spike (RBD Domain) of COVID-19 to Nanomaterial, Protein Ferritin Nanocages.COVID-19 的 SARS-CoV-2 刺突(RBD 结构域)多价展示到纳米材料、蛋白铁蛋白纳米笼上。
Biomolecules. 2021 Feb 17;11(2):297. doi: 10.3390/biom11020297.