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.

Cancer Letters
|April 16, 2023
PubMed

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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