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Published on: February 21, 2025
Application prospect of circular RNA-based neoantigen vaccine in tumor immunotherapy
Mohan Li1, Yian Wang2, Pan Wu3
1NHC Key Laboratory of Carcinogenesis and Hunan Key Laboratory of Cancer Metabolism, Hunan Cancer Hospital and Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China; Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha, Hunan, 410078, China; Department of Pathology, Xiangya Hospital, Central South University, Changsha, Hunan, 410078, China.
Abstract:
Neoantigen is a protein produced by mutant gene, which is only expressed in tumor cells. It is an ideal target for therapeutic tumor vaccines. Although synthetic long peptide (SLP)-based neoantigen vaccine, DNA-based neoantigen vaccine, and mRNA-based neoantigen vaccine are all in the development stage, they have some inherent shortcomings. Therefore, researchers turned their attention to a new type of "non-coding RNA (ncRNA)", circular RNA (circRNA), for potential better choice. Because of its unique high stability and protein-coding capacity, circRNA is a promising target in the field of neoantigen vaccine. In this paper, we reviewed the feasibility of circRNA encoding neoantigens, summarized the construction process, explained the mechanism of circRNA vaccine in vitro, and discussed the advantages and disadvantages of circRNA vaccine and possible combination with other immunotherapies.
Insights
Circular RNA (circRNA) shows promise as a novel platform for neoantigen vaccines, overcoming limitations of current peptide, DNA, and mRNA approaches. This review explores circRNA
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Neoantigens, derived from tumor-specific mutations, are ideal targets for cancer vaccines.
- Current neoantigen vaccine strategies (peptide, DNA, mRNA) face developmental challenges.
- Circular RNA (circRNA) emerges as a novel platform for vaccine development due to its stability and coding potential.
Purpose of the Study:
- To review the feasibility of using circRNA to encode neoantigens for therapeutic vaccines.
- To summarize the construction and in vitro mechanisms of circRNA-based neoantigen vaccines.
- To discuss the advantages, disadvantages, and potential combination immunotherapies for circRNA vaccines.
Main Methods:
- Literature review on circRNA technology in cancer vaccines.
- Analysis of circRNA stability and protein-coding capacity for neoantigen expression.
- Examination of in vitro mechanisms and preclinical data of circRNA vaccines.
- Discussion of comparative advantages over existing vaccine platforms.
Main Results:
- Circular RNA demonstrates high stability and efficient protein translation, making it suitable for neoantigen vaccines.
- The construction of circRNA vaccines involves specific design and production methodologies.
- In vitro studies suggest circRNA vaccines can elicit robust anti-tumor immune responses.
- circRNA vaccines offer potential advantages in terms of immunogenicity and delivery.
Conclusions:
- Circular RNA represents a promising and potentially superior platform for developing next-generation neoantigen vaccines.
- Further research into circRNA vaccine construction and clinical applications is warranted.
- Combination strategies involving circRNA vaccines and other immunotherapies may enhance treatment efficacy.
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