mRNA Vaccine Era—Mechanisms, Drug Platform and Clinical Prospection
Open accessAbstract
Messenger ribonucleic acid (mRNA)-based drugs, notably mRNA vaccines, have been widely proven as a promising treatment strategy in immune therapeutics. The extraordinary advantages associated with mRNA vaccines, including their high efficacy, a relatively low severity of side effects, and low attainment costs, have enabled them to become prevalent in pre-clinical and clinical trials against various infectious diseases and cancers. Recent technological advancements have alleviated some issues that hinder mRNA vaccine development, such as low efficiency that exist in both gene translation and in vivo deliveries. mRNA immunogenicity can also be greatly adjusted as a result of upgraded technologies. In this review, we have summarized details regarding the optimization of mRNA vaccines, and the underlying biological mechanisms of this form of vaccines. Applications of mRNA vaccines in some infectious diseases and cancers are introduced. It also includes our prospections for mRNA vaccine applications in diseases caused by bacterial pathogens, such as tuberculosis. At the same time, some suggestions for future mRNA vaccine development about storage methods, safety concerns, and personalized vaccine synthesis can be found in the context.
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UTRs can influence mRNA translation efficiency and resistance to degradation by interacting with RNA-binding proteins and microRNAs.
“It is known that UTRs are associated with processes of mRNA translation, and by interacting with RNA-binding proteins (RBPs) and microRNAs, UTRs can influence mRNA’s translation efficiency and resistance to degradation [3,4,5,6,7].”
From Untranslated Region Sequences and the Efficacy of mRNA Vaccines against Tuberculosis (2024) · cites this paper as [5]
Section 2.2 (page not provided) says UTRs can alter mRNA decay and translation efficiency through interactions with RNA-binding proteins. Section 2.4 mentions microRNA-mediated translation inhibition in its discussion of the poly(A) tail, but does not say that UTRs interact with microRNAs to produce the claimed effects. (LLM, conf=0.87)
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- Authors
- Xu, S., Yang, K., Li, R., & Zhang, L.
- Affiliations
- Fudan University (CN)
- Peking University (CN)
- Corresponding author
- Zhang, Lu
- ORCID
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2020-09-09
- Volume
- 21
- Issue
- 18
- Pages
- 6582
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC7554980
- OpenAlex
- W3083934582
- Cited by
- 368
- References
- 40
- Citations by year
- 2026: 42 · 2025: 65 · 2024: 65 · 2023: 80 · 2022: 66 · 2021: 49 · 2020: 1
- FWCI
- 4.78
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- the National Key R&D Program of China (No.2018YFD0500900)
- China's 13th Five Year Programs for the prevention and cure of great infectious diseases (2017ZX10201301-005)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Keywords
- mRNA vaccines, mRNA therapeutics, vaccine immunogenicity, infectious disease vaccines, cancer vaccines, tuberculosis, pathogenic bacteria, personalized vaccines, vaccine storage, vaccine safety
- MeSH terms
- Immunogenicity, Vaccine, mRNA Vaccines, RNA, Messenger, Vaccines, Synthetic, Drug Delivery Systems
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