• 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

作为治疗手段的信使核糖核酸:了解信使核糖核酸疫苗。

mRNA as a Therapeutics: Understanding mRNA Vaccines.

作者信息

Oğuz Ferdi, Atmaca Harika

机构信息

Section of Molecular Biology, Department of Biology, Institute of Natural and Applied Sciences, Manisa Celal Bayar University, Muradiye, Manisa, Turkey.

Section of Molecular Biology, Department of Biology, Faculty of Science and Letters, Manisa Celal Bayar University, Muradiye, Manisa, Turkey.

出版信息

Adv Pharm Bull. 2022 Mar;12(2):274-282. doi: 10.34172/apb.2022.028. Epub 2021 May 16.

DOI:10.34172/apb.2022.028
PMID:35620336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9106950/
Abstract

Vaccination is one of the important approaches in the prevention and control of diseases. Although the capacity to present antigens other than the disease-specific antigen in the traditional vaccine composition provides a potential benefit by increasing its protective efficacy, many components that are not needed for the related disease are also transferred. These components can reduce vaccine activity by lowering immunity against protective antigens. The reasons such as the low effectiveness of traditional vaccines and the high cost of production and time-consuming reasons show that it is necessary to develop a new vaccine method for our world, which is struggling with epidemics almost every year. Among nucleic acids, mRNA has many advantages, such as genomic integration, induction of anti-DNA autoantibodies, and immune tolerance induced by long-term antigen expression. mRNA vaccines have become a therapeutic target for reasons such as efficacy, safety, fast and non-expensive production. The fact that mRNA triggers both humoral and cellular immunity and goes only to the cytoplasm, not to the nucleus, makes it highly efficient. The mRNA must cross the lipid bilayer barrier and entry to the cytoplasm where it is translated into protein. There are two main ways of mRNA vaccine delivery for this: ex vivo loading of mRNA into dendritic cells (DCs) and direct injection of mRNA with or without a carrier. Studies continue to understand which delivery system is therapeutically more efficient. Preclinical and clinical trials showed that mRNA vaccines trigger a long-lasting and safe immune response.

摘要

疫苗接种是疾病预防和控制的重要手段之一。尽管传统疫苗组合物中呈现疾病特异性抗原以外的抗原的能力通过提高其保护效力提供了潜在益处,但许多与相关疾病无关的成分也会被传递。这些成分会通过降低对保护性抗原的免疫力来降低疫苗活性。传统疫苗有效性低、生产成本高以及耗时等原因表明,对于几乎每年都在与流行病作斗争的我们的世界而言,开发一种新的疫苗方法是必要的。在核酸中,信使核糖核酸(mRNA)具有许多优势,例如基因组整合、诱导抗DNA自身抗体以及长期抗原表达诱导的免疫耐受。由于有效性、安全性、生产快速且成本低等原因,mRNA疫苗已成为一个治疗靶点。mRNA既能触发体液免疫又能触发细胞免疫,并且仅进入细胞质而非细胞核,这使其具有高效性。mRNA必须穿过脂质双层屏障并进入细胞质,在那里它被翻译成蛋白质。为此,mRNA疫苗递送主要有两种方式:将mRNA体外加载到树突状细胞(DC)中以及直接注射有或没有载体的mRNA。研究仍在继续,以了解哪种递送系统在治疗上更有效。临床前和临床试验表明,mRNA疫苗能触发持久且安全的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3653/9106950/2360236404c9/apb-12-274-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3653/9106950/2360236404c9/apb-12-274-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3653/9106950/2360236404c9/apb-12-274-g001.jpg

相似文献

1
mRNA as a Therapeutics: Understanding mRNA Vaccines.作为治疗手段的信使核糖核酸:了解信使核糖核酸疫苗。
Adv Pharm Bull. 2022 Mar;12(2):274-282. doi: 10.34172/apb.2022.028. Epub 2021 May 16.
2
The Rapid Development and Early Success of Covid 19 Vaccines Have Raised Hopes for Accelerating the Cancer Treatment Mechanism.新冠疫苗的快速研发和早期成功为加速癌症治疗机制带来了希望。
Arch Razi Inst. 2021 Mar;76(1):1-6. doi: 10.22092/ari.2021.353761.1612. Epub 2021 Mar 1.
3
Idiotypic vaccination for B-cell malignancies as a model for therapeutic cancer vaccines: from prototype protein to second generation vaccines.用于B细胞恶性肿瘤的独特型疫苗作为治疗性癌症疫苗的模型:从原型蛋白到第二代疫苗。
Haematologica. 2002 Sep;87(9):989-1001.
4
Fc receptor-targeting of immunogen as a strategy for enhanced antigen loading, vaccination, and protection using intranasally administered antigen-pulsed dendritic cells.将免疫原靶向Fc受体作为一种策略,用于通过鼻内给药的抗原脉冲树突状细胞增强抗原负载、疫苗接种和保护作用。
Vaccine. 2014 Sep 8;32(40):5212-20. doi: 10.1016/j.vaccine.2014.07.050. Epub 2014 Jul 26.
5
[Novel vaccines against M. tuberculosis].[新型抗结核分枝杆菌疫苗]
Kekkaku. 2006 Dec;81(12):745-51.
6
Development of an Antigen Delivery System for a B Cell-Targeted Vaccine as an Alternative to Dendritic Cell-Targeted Vaccines.开发一种用于 B 细胞靶向疫苗的抗原递呈系统,作为树突状细胞靶向疫苗的替代方案。
Chem Pharm Bull (Tokyo). 2022;70(5):341-350. doi: 10.1248/cpb.c22-00047.
7
Lipid-Based Delivery Systems in Development of Genetic and Subunit Vaccines.正在研发中的基因和亚单位疫苗的基于脂质的传递系统。
Mol Biotechnol. 2023 May;65(5):669-698. doi: 10.1007/s12033-022-00624-8. Epub 2022 Dec 3.
8
Preclinical evaluation of mRNA trimannosylated lipopolyplexes as therapeutic cancer vaccines targeting dendritic cells.mRNA 三甘露糖基化脂多聚复合物作为针对树突状细胞的治疗性癌症疫苗的临床前评价。
J Control Release. 2018 May 28;278:110-121. doi: 10.1016/j.jconrel.2018.03.035. Epub 2018 Apr 6.
9
mRNA Vaccines to Protect Against Diseases.用于预防疾病的mRNA疫苗。
Methods Mol Biol. 2022;2410:111-129. doi: 10.1007/978-1-0716-1884-4_5.
10
[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.

引用本文的文献

1
Exploring the Potential and Advancements of Circular RNA Therapeutics.探索环状RNA疗法的潜力与进展。
Exploration (Beijing). 2025 May 1;5(4):e20240044. doi: 10.1002/EXP.20240044. eCollection 2025 Aug.
2
Albumin-recruiting lipid nanoparticle potentiates the safety and efficacy of mRNA vaccines by avoiding liver accumulation.白蛋白募集脂质纳米颗粒通过避免肝脏蓄积增强了mRNA疫苗的安全性和有效性。
Nat Mater. 2025 Aug 1. doi: 10.1038/s41563-025-02284-w.
3
mRNA vaccines in the context of cancer treatment: from concept to application.

本文引用的文献

1
Intracellular Delivery of mRNA in Adherent and Suspension Cells by Vapor Nanobubble Photoporation.通过蒸汽纳米气泡光穿孔实现mRNA在贴壁细胞和悬浮细胞中的细胞内递送。
Nanomicro Lett. 2020 Sep 27;12(1):185. doi: 10.1007/s40820-020-00523-0.
2
mRNA vaccine for cancer immunotherapy.用于癌症免疫治疗的信使核糖核酸疫苗
Mol Cancer. 2021 Feb 25;20(1):41. doi: 10.1186/s12943-021-01335-5.
3
Vaccine Therapies for Cancer: Then and Now.癌症的疫苗疗法:过去与现在。
癌症治疗背景下的mRNA疫苗:从概念到应用
J Transl Med. 2025 Jan 6;23(1):12. doi: 10.1186/s12967-024-06033-6.
4
HBV Vaccines: Advances and Development.乙肝疫苗:进展与发展
Vaccines (Basel). 2023 Dec 18;11(12):1862. doi: 10.3390/vaccines11121862.
5
Just Keep Rolling?-An Encompassing Review towards Accelerated Vaccine Product Life Cycles.持续推进?——关于加速疫苗产品生命周期的全面综述
Vaccines (Basel). 2023 Jul 27;11(8):1287. doi: 10.3390/vaccines11081287.
Target Oncol. 2021 Mar;16(2):121-152. doi: 10.1007/s11523-020-00788-w. Epub 2021 Jan 29.
4
Neo-Antigen mRNA Vaccines.新抗原mRNA疫苗
Vaccines (Basel). 2020 Dec 18;8(4):776. doi: 10.3390/vaccines8040776.
5
Recent advances in mRNA vaccine technology.mRNA 疫苗技术的最新进展。
Curr Opin Immunol. 2020 Aug;65:14-20. doi: 10.1016/j.coi.2020.01.008. Epub 2020 Mar 31.
6
Editorial: Role of CD1- and MR1-Restricted T Cells in Immunity and Disease.社论:CD1 及 MR1 限制型 T 细胞在免疫与疾病中的作用
Front Immunol. 2019 Aug 6;10:1837. doi: 10.3389/fimmu.2019.01837. eCollection 2019.
7
Inside out: optimization of lipid nanoparticle formulations for exterior complexation and in vivo delivery of saRNA.从内到外:用于 saRNA 外部复合和体内递释的脂质纳米粒制剂的优化。
Gene Ther. 2019 Sep;26(9):363-372. doi: 10.1038/s41434-019-0095-2. Epub 2019 Jul 12.
8
A Comparison of Plasmid DNA and mRNA as Vaccine Technologies.质粒DNA与mRNA作为疫苗技术的比较
Vaccines (Basel). 2019 Apr 24;7(2):37. doi: 10.3390/vaccines7020037.
9
Advances in mRNA Vaccines for Infectious Diseases.mRNA 疫苗在传染病防治中的进展
Front Immunol. 2019 Mar 27;10:594. doi: 10.3389/fimmu.2019.00594. eCollection 2019.
10
Segmented poly(A) tails significantly reduce recombination of plasmid DNA without affecting mRNA translation efficiency or half-life.分段 poly(A) 尾显著降低质粒 DNA 的重组,而不影响 mRNA 翻译效率或半衰期。
RNA. 2019 Apr;25(4):507-518. doi: 10.1261/rna.069286.118. Epub 2019 Jan 15.