Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 May 29:15:1394003.
doi: 10.3389/fimmu.2024.1394003. eCollection 2024.

Artificial intelligence and neoantigens: paving the path for precision cancer immunotherapy

Affiliations
Review

Artificial intelligence and neoantigens: paving the path for precision cancer immunotherapy

Alla Bulashevska et al. Front Immunol. .

Abstract

Cancer immunotherapy has witnessed rapid advancement in recent years, with a particular focus on neoantigens as promising targets for personalized treatments. The convergence of immunogenomics, bioinformatics, and artificial intelligence (AI) has propelled the development of innovative neoantigen discovery tools and pipelines. These tools have revolutionized our ability to identify tumor-specific antigens, providing the foundation for precision cancer immunotherapy. AI-driven algorithms can process extensive amounts of data, identify patterns, and make predictions that were once challenging to achieve. However, the integration of AI comes with its own set of challenges, leaving space for further research. With particular focus on the computational approaches, in this article we have explored the current landscape of neoantigen prediction, the fundamental concepts behind, the challenges and their potential solutions providing a comprehensive overview of this rapidly evolving field.

Keywords: artificial intelligence; cancer immunotherapy; immunopeptidomics; neoantigen prediction; precision medicine.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Schematic overview of AI algorithm training on public databases. A group of subjects, specific for the condition of interest is chosen for the experimental procedures. After completing the experimental pipelines, the generated data is stored in a public database. AI algorithms can then be trained on these datasets.
Figure 2
Figure 2
Steps of neoantigen selection from patient data. A set of diagnostic procedures are completed on patient derived samples. Ideally all of the above-mentioned patient data (WES, WGS, HLA typing, RNA-seq) are available before proceeding. After a candidate peptide selection is generated from the patient data, the AI model of preference is applied. The AI model will compute a ranked peptide list from the candidate peptides. Careful design of personalized vaccine is available, based on the peptide rankings.
Figure 3
Figure 3
NGS-based HLA genotyping. Sequence data generated by sequencing technologies is mapped against the reference allele repository (IPD-IMGT). Corresponding to the HLA genotyping algorithm used either the raw reads or assembled contigs are aligned.
Figure 4
Figure 4
Challenges and potential solutions to promote widespread clinical use of AI applications for neoantigens discovery. We distinguish challenges that must be addressed for successful AI integration into clinical praxis as related to data, models, AI architecture and technical integration. For each group of challenges we list various algorithmic, experimental and organizational approaches carrying the potential to overcome the respective challenges.

Similar articles

Cited by

References

    1. Haen SP, Löffler MW, Rammensee H-G, Brossart P. Towards new horizons: characterization, classification and implications of the tumour antigenic repertoire. Nat Rev Clin Oncol. (2020) 17:595–610. doi: 10.1038/s41571-020-0387-x - DOI - PMC - PubMed
    1. Sahin U, Türeci Ö. Personalized vaccines for cancer immunotherapy. Science. (2018) 359:1355–60. doi: 10.1126/science.aar7112 - DOI - PubMed
    1. Hu Z, Leet DE, Allesøe RL, Oliveira G, Li S, Luoma AM, et al. . Personal neoantigen vaccines induce persistent memory T cell responses and epitope spreading in patients with melanoma. Nat Med. (2021) 27:515–25. doi: 10.1038/s41591-020-01206-4 - DOI - PMC - PubMed
    1. Rojas LA, Sethna Z, Soares KC, Olcese C, Pang N, Patterson E, et al. . Personalized RNA neoantigen vaccines stimulate T cells in pancreatic cancer. Nature. (2023) 618:144–50. doi: 10.1038/s41586-023-06063-y - DOI - PMC - PubMed
    1. Aurisicchio L, Pallocca M, Ciliberto G, Palombo F. The perfect personalized cancer therapy: cancer vaccines against neoantigens. J Exp Clin Cancer Res. (2018) 37:86. doi: 10.1186/s13046-018-0751-1 - DOI - PMC - PubMed

Substances