Neoantigens: promising targets for cancer therapy.
Na XieGuobo ShenWei GaoZhao HuangCanhua HuangLi FuPublished in: Signal transduction and targeted therapy (2023)
Recent advances in neoantigen research have accelerated the development and regulatory approval of tumor immunotherapies, including cancer vaccines, adoptive cell therapy and antibody-based therapies, especially for solid tumors. Neoantigens are newly formed antigens generated by tumor cells as a result of various tumor-specific alterations, such as genomic mutation, dysregulated RNA splicing, disordered post-translational modification, and integrated viral open reading frames. Neoantigens are recognized as non-self and trigger an immune response that is not subject to central and peripheral tolerance. The quick identification and prediction of tumor-specific neoantigens have been made possible by the advanced development of next-generation sequencing and bioinformatic technologies. Compared to tumor-associated antigens, the highly immunogenic and tumor-specific neoantigens provide emerging targets for personalized cancer immunotherapies, and serve as prospective predictors for tumor survival prognosis and immune checkpoint blockade responses. The development of cancer therapies will be aided by understanding the mechanism underlying neoantigen-induced anti-tumor immune response and by streamlining the process of neoantigen-based immunotherapies. This review provides an overview on the identification and characterization of neoantigens and outlines the clinical applications of prospective immunotherapeutic strategies based on neoantigens. We also explore their current status, inherent challenges, and clinical translation potential.
Keyphrases
- cell therapy
- immune response
- papillary thyroid
- cancer therapy
- squamous cell
- dendritic cells
- drug delivery
- current status
- transcription factor
- toll like receptor
- squamous cell carcinoma
- sars cov
- risk assessment
- young adults
- inflammatory response
- dna methylation
- endothelial cells
- lymph node metastasis
- mesenchymal stem cells
- working memory
- genome wide
- free survival
- human health