• 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

基于体外转录RNA的平台疫苗:过去、现在与未来

In Vitro Transcribed RNA-Based Platform Vaccines: Past, Present, and Future.

作者信息

Perenkov Alexey D, Sergeeva Alena D, Vedunova Maria V, Krysko Dmitri V

机构信息

Institute of Biology and Biomedicine, National Research Lobachevsky State University of Nizhny Novgorod, 603022 Nizhny Novgorod, Russia.

Cell Death Investigation and Therapy (CDIT) Laboratory, Anatomy and Embryology Unit, Department of Human Structure and Repair, Faculty of Medicine and Health Science, Ghent University, 9000 Ghent, Belgium.

出版信息

Vaccines (Basel). 2023 Oct 16;11(10):1600. doi: 10.3390/vaccines11101600.

DOI:10.3390/vaccines11101600
PMID:37897003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10610676/
Abstract

mRNA was discovered in 1961, but it was not used as a vaccine until after three decades. Recently, the development of mRNA vaccine technology gained great impetus from the pursuit of vaccines against COVID-19. To improve the properties of RNA vaccines, and primarily their circulation time, self-amplifying mRNA and trans-amplifying mRNA were developed. A separate branch of mRNA technology is circular RNA vaccines, which were developed with the discovery of the possibility of translation on their protein matrix. Circular RNA has several advantages over mRNA vaccines and is considered a fairly promising platform, as is trans-amplifying mRNA. This review presents an overview of the mRNA platform and a critical discussion of the more modern self-amplifying mRNA, trans-amplifying mRNA, and circular RNA platforms created on its basis. Finally, the main features, advantages, and disadvantages of each of the presented mRNA platforms are discussed. This discussion will facilitate the decision-making process in selecting the most appropriate platform for creating RNA vaccines against cancer or viral diseases.

摘要

信使核糖核酸(mRNA)于1961年被发现,但直到三十年后才被用作疫苗。最近,mRNA疫苗技术的发展因对抗新冠病毒疫苗的研发而获得了巨大推动力。为了改善RNA疫苗的特性,主要是其循环时间,人们开发了自我扩增mRNA和转扩增mRNA。mRNA技术的一个独立分支是环状RNA疫苗,它是随着在其蛋白质基质上进行翻译的可能性被发现而开发的。环状RNA相对于mRNA疫苗具有若干优势,并且被认为是一个相当有前景的平台,转扩增mRNA也是如此。本文综述了mRNA平台,并对在其基础上创建的更现代的自我扩增mRNA、转扩增mRNA和环状RNA平台进行了批判性讨论。最后,讨论了所介绍的每个mRNA平台的主要特点、优点和缺点。这一讨论将有助于在选择最适合的平台来研发针对癌症或病毒性疾病的RNA疫苗时的决策过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/65b682aaa999/vaccines-11-01600-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/0a86bf0777bf/vaccines-11-01600-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/daa7800f2853/vaccines-11-01600-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/ecf34bc3ba31/vaccines-11-01600-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/2bf4a1fefb27/vaccines-11-01600-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/0322869597cf/vaccines-11-01600-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/8d71e9f0deac/vaccines-11-01600-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/1e4ad4b3d62c/vaccines-11-01600-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/eb79b3cd402a/vaccines-11-01600-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/65b682aaa999/vaccines-11-01600-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/0a86bf0777bf/vaccines-11-01600-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/daa7800f2853/vaccines-11-01600-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/ecf34bc3ba31/vaccines-11-01600-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/2bf4a1fefb27/vaccines-11-01600-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/0322869597cf/vaccines-11-01600-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/8d71e9f0deac/vaccines-11-01600-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/1e4ad4b3d62c/vaccines-11-01600-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/eb79b3cd402a/vaccines-11-01600-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ae/10610676/65b682aaa999/vaccines-11-01600-g009.jpg

相似文献

1
In Vitro Transcribed RNA-Based Platform Vaccines: Past, Present, and Future.基于体外转录RNA的平台疫苗:过去、现在与未来
Vaccines (Basel). 2023 Oct 16;11(10):1600. doi: 10.3390/vaccines11101600.
2
The Importance of RNA-Based Vaccines in the Fight against COVID-19: An Overview.基于RNA的疫苗在抗击新冠疫情中的重要性:概述
Vaccines (Basel). 2021 Nov 17;9(11):1345. doi: 10.3390/vaccines9111345.
3
Trans-Amplifying RNA: A Journey from Alphavirus Research to Future Vaccines.反式扩增RNA:从甲病毒研究到未来疫苗的历程
Viruses. 2024 Mar 25;16(4):503. doi: 10.3390/v16040503.
4
Trans-Amplifying RNA Vaccines Against Infectious Diseases: A Comparison with Non-Replicating and Self-Amplifying RNA.针对传染病的反式扩增RNA疫苗:与非复制型和自我扩增型RNA的比较
Methods Mol Biol. 2024;2786:135-144. doi: 10.1007/978-1-0716-3770-8_5.
5
mRNA vaccines: Past, present, future.信使核糖核酸疫苗:过去、现在与未来。
Asian J Pharm Sci. 2022 Jul;17(4):491-522. doi: 10.1016/j.ajps.2022.05.003. Epub 2022 Jun 30.
6
Immunogenicity and safety of a booster dose of a self-amplifying RNA COVID-19 vaccine (ARCT-154) versus BNT162b2 mRNA COVID-19 vaccine: a double-blind, multicentre, randomised, controlled, phase 3, non-inferiority trial.一种自我扩增 RNA COVID-19 疫苗(ARCT-154)与 BNT162b2 mRNA COVID-19 疫苗加强针的免疫原性和安全性:一项双盲、多中心、随机、对照、3 期、非劣效性试验。
Lancet Infect Dis. 2024 Apr;24(4):351-360. doi: 10.1016/S1473-3099(23)00650-3. Epub 2023 Dec 20.
7
Self-amplifying mRNA-Based Vaccine Technology and Its Mode of Action.基于自我扩增信使 RNA 的疫苗技术及其作用模式。
Curr Top Microbiol Immunol. 2022;440:31-70. doi: 10.1007/82_2021_233.
8
The role of nanoparticle format and route of administration on self-amplifying mRNA vaccine potency.纳米颗粒形式和给药途径对自扩增 mRNA 疫苗效力的影响。
J Control Release. 2022 Feb;342:388-399. doi: 10.1016/j.jconrel.2021.12.008. Epub 2021 Dec 10.
9
[New Hopes in Vaccine Technology: mRNA Vaccines].[疫苗技术的新希望:信使核糖核酸疫苗]
Mikrobiyol Bul. 2021 Apr;55(2):265-284. doi: 10.5578/mb.20219912.
10
Amplifying mRNA vaccines: potential versatile magicians for oncotherapy.mRNA 疫苗增效剂:肿瘤治疗的潜在多面手。
Front Immunol. 2023 Oct 23;14:1261243. doi: 10.3389/fimmu.2023.1261243. eCollection 2023.

引用本文的文献

1
Research progress of mRNA vaccines for infectious diseases.传染病mRNA疫苗的研究进展
Eur J Med Res. 2025 Aug 23;30(1):792. doi: 10.1186/s40001-025-03060-x.
2
Unraveling the advances of non-coding RNAs on the tumor microenvironment: innovative strategies for cancer therapies.解析非编码RNA在肿瘤微环境中的进展:癌症治疗的创新策略。
J Transl Med. 2025 Jun 2;23(1):614. doi: 10.1186/s12967-025-06629-6.
3
Revolutionizing immunization: a comprehensive review of mRNA vaccine technology and applications.免疫接种的变革:mRNA疫苗技术与应用的全面综述

本文引用的文献

1
Engineering a Circular Riboregulator in .在……中构建一个环状核糖调节子
Biodes Res. 2020 Sep 12;2020:1916789. doi: 10.34133/2020/1916789. eCollection 2020.
2
Efficient circular RNA engineering by end-to-end self-targeting and splicing reaction using group I intron ribozyme.利用I组内含子核酶通过端到端自靶向和剪接反应实现高效环状RNA工程。
Mol Ther Nucleic Acids. 2023 Aug 1;33:587-598. doi: 10.1016/j.omtn.2023.07.034. eCollection 2023 Sep 12.
3
Recent Advancement in mRNA Vaccine Development and Applications.mRNA疫苗开发与应用的最新进展
Virol J. 2025 Mar 12;22(1):71. doi: 10.1186/s12985-025-02645-6.
4
mRNA cancer vaccines from bench to bedside: a new era in cancer immunotherapy.从实验室到临床的mRNA癌症疫苗:癌症免疫治疗的新时代。
Biomark Res. 2024 Dec 18;12(1):157. doi: 10.1186/s40364-024-00692-9.
5
New insights for the development of efficient DNA vaccines.为开发高效的 DNA 疫苗提供新的见解。
Microb Biotechnol. 2024 Nov;17(11):e70053. doi: 10.1111/1751-7915.70053.
6
mRNA vaccines in tumor targeted therapy: mechanism, clinical application, and development trends.mRNA疫苗在肿瘤靶向治疗中的作用机制、临床应用及发展趋势
Biomark Res. 2024 Aug 31;12(1):93. doi: 10.1186/s40364-024-00644-3.
7
Biogenesis and Function of circRNAs in Pulmonary Fibrosis.环状 RNA 在肺纤维化中的生成和功能。
Curr Gene Ther. 2024;24(5):395-409. doi: 10.2174/0115665232284076240207073542.
8
The inorganic pyrophosphatases of microorganisms: a structural and functional review.微生物的无机焦磷酸酶:结构与功能综述。
PeerJ. 2024 Jun 24;12:e17496. doi: 10.7717/peerj.17496. eCollection 2024.
9
Recent Findings on Therapeutic Cancer Vaccines: An Updated Review.治疗性癌症疫苗的最新研究成果:最新综述
Biomolecules. 2024 Apr 21;14(4):503. doi: 10.3390/biom14040503.
Pharmaceutics. 2023 Jul 18;15(7):1972. doi: 10.3390/pharmaceutics15071972.
4
Cap-Independent Circular mRNA Translation Efficiency.帽依赖性环状mRNA翻译效率
Vaccines (Basel). 2023 Jan 20;11(2):238. doi: 10.3390/vaccines11020238.
5
Differences in the immunogenicity of engineered circular RNAs.工程化环状RNA免疫原性的差异。
J Mol Cell Biol. 2023 Jun 1;15(1). doi: 10.1093/jmcb/mjad002.
6
A Comprehensive Review of mRNA Vaccines.mRNA 疫苗的全面综述。
Int J Mol Sci. 2023 Jan 31;24(3):2700. doi: 10.3390/ijms24032700.
7
mRNA vaccines: The future of prevention of viral infections?信使核糖核酸疫苗:预防病毒感染的未来方向?
J Med Virol. 2023 Feb;95(2):e28572. doi: 10.1002/jmv.28572.
8
Research progress on circular RNA vaccines.环状 RNA 疫苗的研究进展。
Front Immunol. 2023 Jan 12;13:1091797. doi: 10.3389/fimmu.2022.1091797. eCollection 2022.
9
A trans-amplifying RNA simplified to essential elements is highly replicative and robustly immunogenic in mice.一种简化为基本元件的跨扩增 RNA 在小鼠中具有高度的复制能力和强大的免疫原性。
Mol Ther. 2023 Jun 7;31(6):1636-1646. doi: 10.1016/j.ymthe.2023.01.019. Epub 2023 Jan 23.
10
Self-Amplifying RNA Vaccine Candidates: Alternative Platforms for mRNA Vaccine Development.自我扩增RNA疫苗候选物:mRNA疫苗开发的替代平台
Pathogens. 2023 Jan 13;12(1):138. doi: 10.3390/pathogens12010138.