The DOI matches its Crossref record; 319 of the 319 references it cites were found in a registry or an index.
Circular RNA vaccine in disease prevention and treatment
Open accessAbstract
CircRNAs are a class of single-stranded RNAs with covalently linked head-to-tail topology. In the decades since its initial discovery, their biogenesis, regulation, and function have rapidly disclosed, permitting a better understanding and adoption of them as new tools for medical applications. With the development of biotechnology and molecular medicine, artificial circRNAs have been engineered as a novel class of vaccines for disease treatment and prevention. Unlike the linear mRNA vaccine which applications were limited by its instability, inefficiency, and innate immunogenicity, circRNA vaccine which incorporate internal ribosome entry sites (IRESs) and open reading frame (ORF) provides an improved approach to RNA-based vaccination with safety, stability, simplicity of manufacture, and scalability. However, circRNA vaccines are at an early stage, and their optimization, delivery and applications require further development and evaluation. In this review, we comprehensively describe circRNA vaccine, including their history and superiority. We also summarize and discuss the current methodological research for circRNA vaccine preparation, including their design, synthesis, and purification. Finally, we highlight the delivery options of circRNA vaccine and its potential applications in diseases treatment and prevention. Considering their unique high stability, low immunogenicity, protein/peptide-coding capacity and special closed-loop construction, circRNA vaccine, and circRNA-based therapeutic platforms may have superior application prospects in a broad range of diseases.
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Cites
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BackgroundCryo-EM structure of the 2019-nCoV spike in the prefusion conformation
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Circular RNAs are abundant, conserved, and associated with ALU repeats
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Direct Gene Transfer into Mouse Muscle in Vivo
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“206 fi rst RNA-based vaccine candidate developed in 1993 was proven to induce both humoral and cellular immunity in vivo but exhibited unfavorable safety pro fi les and was susceptible to immune recognition and degradation by RNases.”
Background
Metadata
- Authors
- Niu, D., Wu, Y., & Lian, J.
- Venue
- Signal Transduction and Targeted Therapy
- Published
- 2023-09-11
- Volume
- 8
- Issue
- 1
- Pages
- 341-341
- ISSN
- 2059-3635 (ISSN-L)
- OpenAlex
- W4386582940
- Cited by
- 267
- References
- 319
- FWCI
- 20.02
- Type
- journal article
- Language
- en
- Open access
- gold
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