免疫原性
序列(生物学)
人工神经网络
计算生物学
主要组织相容性复合体
计算机科学
肽
人工智能
生物
免疫学
抗原
遗传学
生物化学
作者
Smita Krishnaswamy,Kevin B. Givechian,João Rocha,Edward Yang,Chen Liu,Kerrie Greene,Rex Ying,Étienne Caron,Akiko Iwasaki
出处
期刊:Research Square
日期:2025-05-21
被引量:1
标识
DOI:10.21203/rs.3.rs-6606336/v1
摘要
Abstract Epitope-based vaccines are promising therapeutic modalities for infectious diseases and cancer, but identifying immunogenic epitopes is challenging. The vast majority of prediction methods only use amino acid sequence information, and do not incorporate wide-scale structure data and biochemical properties across each peptide-MHC. We present ImmunoStruct, a deep-learning model that integrates sequence, structural, and biochemical information to predict multi-allele class-I peptide-MHC immunogenicity. By leveraging a multimodal dataset of ∼27,000 peptide-MHCs, we demonstrate that ImmunoStruct improves immunogenicity prediction performance and interpretability beyond existing methods, across infectious disease epitopes and cancer neoepitopes. We further show strong alignment with in vitro assay results for a set of SARS-CoV-2 epitopes, as well as strong performance in peptide-MHC-based cancer patient survival prediction. Overall, this work also presents a new architecture that incorporates equivariant graph processing and multimodal data integration for the long standing task in immunotherapy.
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