Advancements of in vitro transcribed mRNA (IVT mRNA) to enable translation into the clinics
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The accelerated progress and approval of two mRNA-based vaccines to address the SARS-CoV-2 virus were unprecedented. This record-setting feat was made possible through the solid foundation of research on in vitro transcribed mRNA (IVT mRNA) which could be utilized as a therapeutic modality. Through decades of thorough research to overcome barriers to implementation, mRNA-based vaccines or therapeutics offer many advantages to rapidly address a broad range of applications including infectious diseases, cancers, and gene editing. Here, we describe the advances that have supported the adoption of IVT mRNA in the clinics, including optimization of the IVT mRNA structural components, synthesis, and lastly concluding with different classes of IVT RNA. Continuing interest in driving IVT mRNA technology will enable a safer and more efficacious therapeutic modality to address emerging and existing diseases.
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UTRs and the poly(A) tail play a crucial role in regulating mRNA intracellular kinetics.
“Untranslated regions (UTRs) and the poly(A) tail play a crucial role in regulating mRNA intracellular kinetics.”
From Evaluation of synthetic mRNA with selected UTR sequences and alternative poly(A) tail, in vitro and in vivo (2025) · cites this paper as [4]
Vaccination is the only approved application of synthetic mRNA.
“Vaccination is the only approved application of synthetic mRNA.2,4”
From Evaluation of synthetic mRNA with selected UTR sequences and alternative poly(A) tail, in vitro and in vivo (2025) · cites this paper as [4]
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Cited by
Sorted by citations
Medjmedj, A., Genon, H., Hezili, D., Loth, A. N., Clemençon, R., Guimpied, C., Mollet, L., Bigot, A., Wien, F., Hamacek, J., et al. (2025) · Molecular Therapy Nucleic Acids · doi:10.1016/j.omtn.2025.102648 · Cited by 19 · see citing works
- Authors
- Kang, D. D., Li, H., & Dong, Y.
- Affiliations
- Tisch Cancer Institute (US)
- Corresponding author
- Dong, Yizhou
- Venue
- Advanced Drug Delivery Reviews
- Publisher
- Elsevier BV
- Published
- 2023-08
- Volume
- 199
- Pages
- 114961
- ISSN
- 0169-409X (ISSN-L)
- PMC
- PMC10264168
- OpenAlex
- W4380793095
- Cited by
- 100
- References
- 35
- Citations by year
- 2026: 21 · 2025: 47 · 2024: 28 · 2023: 4
- FWCI
- 2.58
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (am, 323 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Advanced Drug Delivery Reviews (acceptedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R35GM144117)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- in vitro transcribed mRNA, mRNA vaccines, mRNA therapeutics, SARS-CoV-2, mRNA synthesis, genome editing, clinical translation
- MeSH terms
- COVID-19, SARS-CoV-2, Humans, Neoplasms, RNA, Messenger, Vaccines
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