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METHODS article

Front. Immunol.
Sec. Systems Immunology
Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1550252
This article is part of the Research Topic Artificial Intelligence for Cancer Immunotherapy View all 4 articles

OnmiMHC: A Machine Learning Solution for UCEC Tumor Vaccine Development through Enhanced Peptide-MHC Binding Prediction

Provisionally accepted
  • 1 Shanghai Jiao Tong University, Shanghai, China
  • 2 DigitalGene, Ltd, Shanghai, China
  • 3 State Key Laboratory of Biochemical Engineering, Institute of Process Engineering (CAS), Beijing, Beijing Municipality, China

The final, formatted version of the article will be published soon.

    The key roles of Major Histocompatibility Complex (MHC) Class I and II molecules in the immune system are well established. This study aims to develop a novel machine learning framework for predicting antigen peptide presentation by MHC Class I and II molecules. By integrating large-scale mass spectrometry data and other relevant data types, we present a prediction model OnmiMHC based on deep learning. We rigorously assessed its performance using an independent test set, OnmiMHC achieves a PR-AUC score of 0.854 and a TOP20%-PPV of 0.934 in the MHC-I task, which outperforms existing methods. Likewise, in the domain of MHC-II prediction, our model OnmiMHC exhibits a PR-AUC score of 0.606 and a TOP20%-PPV of 0.690, outperforming other baseline methods. These results demonstrate the superiority of our model OnmiMHC in accurately predicting peptide-MHC binding affinities across both MHC-I and MHC-II molecules. With its superior accuracy and predictive capability, our model not only excels in general predictive tasks but also achieves significant results in the prediction of neoantigens for specific cancer types. Particularly for Uterine Corpus Endometrial Carcinoma (UCEC), our model has successfully predicted neoantigens with a high binding probability to common human alleles. This discovery is of great significance for the development of personalized tumor vaccines targeting UCEC.

    Keywords: Peptide-MHC binding, MHC I and II, deep learning, Uterine corpus endometrial carcinoma, neoantigen

    Received: 23 Dec 2024; Accepted: 03 Feb 2025.

    Copyright: © 2025 Jian, Cai, Chen, Pan, Feng and Yuan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Ye Yuan, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering (CAS), Beijing, 100190, Beijing Municipality, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.