PepSim: T-cell cross-reactivity prediction via comparison of peptide sequence and peptide-HLA structure

被引:0
|
作者
Hall-Swan, Sarah [1 ]
Slone, Jared [1 ]
Rigo, Mauricio M. [1 ]
Antunes, Dinler A. [2 ]
Lizee, Gregory [3 ]
Kavraki, Lydia E. [1 ]
机构
[1] Rice Univ, Dept Comp Sci, Houston, TX 77005 USA
[2] Univ Houston, Dept Biol & Biochem, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX USA
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
T-cell cross-reactivity; peptide-HLA; immunotherapy; structure comparison; sequence similarity; GENOTYPE-REACTIVITY;
D O I
10.3389/fimmu.2023.1108303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionPeptide-HLA class I (pHLA) complexes on the surface of tumor cells can be targeted by cytotoxic T-cells to eliminate tumors, and this is one of the bases for T-cell-based immunotherapies. However, there exist cases where therapeutic T-cells directed towards tumor pHLA complexes may also recognize pHLAs from healthy normal cells. The process where the same T-cell clone recognizes more than one pHLA is referred to as T-cell cross-reactivity and this process is driven mainly by features that make pHLAs similar to each other. T-cell cross-reactivity prediction is critical for designing T-cell-based cancer immunotherapies that are both effective and safe. MethodsHere we present PepSim, a novel score to predict T-cell cross-reactivity based on the structural and biochemical similarity of pHLAs. Results and discussionWe show our method can accurately separate cross-reactive from non-crossreactive pHLAs in a diverse set of datasets including cancer, viral, and self-peptides. PepSim can be generalized to work on any dataset of class I peptide-HLAs and is freely available as a web server at pepsim.kavrakilab.org.
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页数:13
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