免疫原性
人类白细胞抗原
计算生物学
表位
主要组织相容性复合体
肽
肽疫苗
免疫疗法
免疫系统
抗原
计算机科学
免疫学
医学
生物
生物化学
作者
Jingcheng Wu,Wenzhe Wang,Jiucheng Zhang,Binbin Zhou,Wenyi Zhao,Zhixi Su,Xun Gu,Jian Wu,Zhan Zhou,Shuqing Chen
标识
DOI:10.3389/fimmu.2019.02559
摘要
Neoantigens play important roles in cancer immunotherapy. Current methods used for neoantigen prediction focus on the binding between human leukocyte antigens (HLAs) and peptides, which is insufficient for high-confidence neoantigen prediction. In this study, we apply deep learning techniques to predict neoantigens considering both the possibility of HLA-peptide binding (binding model) and the potential immunogenicity (immunogenicity model) of the peptide-HLA complex (pHLA). The binding model achieves comparable performance with other well-acknowledged tools on the latest Immune Epitope Database (IEDB) benchmark datasets and an independent mass spectrometry (MS) dataset. The immunogenicity model could significantly improve the prediction precision of neoantigens. The further application of our method to the mutations with pre-existing T-cell responses indicating its feasibility in clinical application. DeepHLApan is freely available at https://github.com/jiujiezz/deephlapan and http://biopharm.zju.edu.cn/deephlapan.
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