Author
Listed:
- Jinhao Que
(Harbin Institute of Technology)
- Guangfu Xue
(Harbin Institute of Technology)
- Tao Wang
(Northwestern Polytechnical University)
- Xiyun Jin
(Harbin Medical University)
- Zuxiang Wang
(Harbin Medical University)
- Yideng Cai
(Harbin Institute of Technology)
- Wenyi Yang
(Harbin Institute of Technology)
- Meng Luo
(Harbin Institute of Technology)
- Qian Ding
(Harbin Institute of Technology)
- Jinwei Zhang
(Harbin Institute of Technology)
- Yilin Wang
(Harbin Institute of Technology)
- Yuexin Yang
(Harbin Institute of Technology)
- Fenglan Pang
(Harbin Institute of Technology)
- Yi Hui
(Harbin Institute of Technology)
- Zheng Wei
(Harbin Institute of Technology)
- Jun Xiong
(Harbin Institute of Technology)
- Shouping Xu
(Harbin Medical University Cancer Hospital)
- Yi Lin
(Harbin Medical University)
- Haoxiu Sun
(Harbin Medical University)
- Pingping Wang
(Harbin Medical University)
- Zhaochun Xu
(Harbin Medical University)
- Qinghua Jiang
(Harbin Institute of Technology
Harbin Medical University
Harbin Medical University)
Abstract
Precise identification of T cell antigens in silico is crucial for the development of cancer mRNA vaccines. However, current computational methods only utilize sequence-level rather than atomic level features to identify T cell antigens, which results in poor representation of those that activate immune responses. Here we propose deepAntigen, a graph convolutional network-based framework, to identify T cell antigens at the atomic level. deepAntigen achieves excellent performance both in the prediction of antigen-human leukocyte antigen (HLA) binding and antigen-T cell receptor (TCR) interactions, which can provide comprehensive guidance for identification of T cell antigens. The tumor neoantigens predicted by deepAntigen in lung, breast and pancreatic cancer patients are experimentally validated through ELISPOT assays, which detect successful activation of CD8+ T cells to release IFN-γ. Overall, deepAntigen can accurately identify T cell antigens at the atomic level, which could accelerate the development of personalized neoantigen targeted immunotherapies for cancer patients.
Suggested Citation
Jinhao Que & Guangfu Xue & Tao Wang & Xiyun Jin & Zuxiang Wang & Yideng Cai & Wenyi Yang & Meng Luo & Qian Ding & Jinwei Zhang & Yilin Wang & Yuexin Yang & Fenglan Pang & Yi Hui & Zheng Wei & Jun Xion, 2025.
"Identifying T cell antigen at the atomic level with graph convolutional network,"
Nature Communications, Nature, vol. 16(1), pages 1-19, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60461-6
DOI: 10.1038/s41467-025-60461-6
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