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

被引:13
作者
Perenkov, Alexey D. [1 ]
Sergeeva, Alena D. [1 ]
Vedunova, Maria V. [1 ]
Krysko, Dmitri V. [1 ,2 ,3 ]
机构
[1] Natl Res Lobachevsky State Univ Nizhny Novgorod, Inst Biol & Biomed, Nizhnii Novgorod 603022, Russia
[2] Univ Ghent, Fac Med & Hlth Sci, Dept Human Struct & Repair, Anat & Embryol Unit,Cell Death Invest & Therapy CD, B-9000 Ghent, Belgium
[3] Canc Res Inst Ghent, B-9000 Ghent, Belgium
基金
俄罗斯科学基金会;
关键词
mRNA vaccine; self-amplifying mRNA vaccine; trans-amplifying mRNA vaccine; circular RNA vaccine; immunogenicity; vaccine; REVERSE CAP ANALOGS; MESSENGER-RNA; CIRCULAR RNAS; CHEMICAL-MODIFICATION; IMMUNE-RESPONSE; GENE-EXPRESSION; 3' UTRS; SELF; TRANSLATION; RECOGNITION;
D O I
10.3390/vaccines11101600
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:31
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共 202 条
  • [1] Abe N, 2018, METHODS MOL BIOL, V1724, P181, DOI 10.1007/978-1-4939-7562-4_15
  • [2] Nonstructural Proteins of AlphavirusPotential Targets for Drug Development
    Abu Bakar, Farhana
    Ng, Lisa F. P.
    [J]. VIRUSES-BASEL, 2018, 10 (02):
  • [3] Designing a novel mRNA vaccine against SARS-CoV-2: An immunoinformatics approach
    Ahammad, Ishtiaque
    Lira, Samia Sultana
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 162 : 820 - 837
  • [4] Recent Advancement in mRNA Vaccine Development and Applications
    Al Fayez, Nojoud
    Nassar, Majed S.
    Alshehri, Abdullah A.
    Alnefaie, Meshal K.
    Almughem, Fahad A.
    Alshehri, Bayan Y.
    Alawad, Abdullah O.
    Tawfik, Essam A.
    [J]. PHARMACEUTICS, 2023, 15 (07)
  • [5] The role of lipid components in lipid nanoparticles for vaccines and gene therapy
    Albertsen, Camilla Hald
    Kulkarni, Jayesh A.
    Witzigmann, Dominik
    Lind, Marianne
    Petersson, Karsten
    Simonsen, Jens B.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2022, 188
  • [6] Exploring dengue genome to construct a multi-epitope based subunit vaccine by utilizing immunoinformatics approach to battle against dengue infection
    Ali, Mudassar
    Pandey, Rajan Kumar
    Khatoon, Nazia
    Narula, Aruna
    Mishra, Amit
    Prajapati, Vijay Kumar
    [J]. SCIENTIFIC REPORTS, 2017, 7
  • [7] [Anonymous], TRILINK BIOTECHNOLOG
  • [8] Research progress on circular RNA vaccines
    Bai, Yu
    Liu, Dong
    He, Qian
    Liu, Jianyang
    Mao, Qunying
    Liang, Zhenglun
    [J]. FRONTIERS IN IMMUNOLOGY, 2023, 13
  • [9] A Facile Method for the Removal of dsRNA Contaminant from In Vitro-Transcribed mRNA
    Baiersdoerfer, Markus
    Boros, Gabor
    Muramatsu, Hiromi
    Mahiny, Azita
    Vlatkovic, Irena
    Sahin, Ugur
    Kariko, Katalin
    [J]. MOLECULAR THERAPY-NUCLEIC ACIDS, 2019, 15 : 26 - 35
  • [10] Banerjee S, 2020, bioRxiv, DOI [10.1101/2020.07.23.218529, 10.1101/2020.07.23.218529, DOI 10.1101/2020.07.23.218529]