Quantitative and large-scale investigation of human TCR-HLA Cross-Reactivity
Pan, M.; Tan, Y.; Tracy, W. Y.; Hu, J.; Fleming, J.; Hu, H.; Yang, Z.; Zhan, X.; Li, B.
Show abstract
The interaction between Human leukocyte antigens (HLA) and T cell receptor (TCR) is essential for adaptive immune recognition. While it is known that one TCR can map to multiple HLA alleles, the extent of this cross-reactivity remains poorly understood. Here, we introduce THNet, a TCR-based HLA similarity inference method, and performed a comprehensive analysis of HLA-TCR cross-reactivity. This method is built upon clustering over 47 million TCRs to identify over 9 million significant HLA-TCR pairs. We created similarity networks for both class I and class II HLA alleles, illustrating how peptide cross-presentation contributes to HLA-TCR cross-reactivity. This analysis revealed novel disease-susceptibilities missed by single-HLA enrichment analyses, especially in the Black populations. Finally, we demonstrated that THNet prioritized optimal HLA mismatch candidates for organ transplantation, thereby improving patient survival rates. Our investigation of HLA-TCR cross-reactive network might provide useful insights for autoimmune risk prediction and better transplantation outcomes. One Sentence SummaryWe introduced THNet, a large-scale TCR-based HLA similarity mapping network that uncovers previously unrecognized cross-reactivity patterns across HLA alleles and provides valuable insights into their influence on disease susceptibility and graft rejection.
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Probabilities of HIV-1 bNAb development in healthy and chronically infected individuals 95%
- Single-Cell Profiling of the Antigen-Specific Response to BNT162b2 SARS-CoV-2 RNA Vaccine 95%
- NeoPrecis: Enhancing Immunotherapy Response Prediction through Integration of Qualified Immunogenicity and Clonality-Aware Neoantigen Landscapes 95%
Similar papers in this journal
- MIST: an interpretable and flexible deep learning framework for single-T cell transcriptome and receptor analysis 96%
- Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers 94%
- TET2 regulates early and late transitions in exhausted CD8+ T-cell differentiation and limits CAR T-cell function 94%
Similar papers in this journal
- Integrated single-cell transcriptomics and epigenomics reveals strong germinal center-associated etiology of autoimmune risk loci 96%
- Computational prediction of MHC anchor locations guide neoantigen identification and prioritization 95%
- Single-Cell Multiomics Defines Tolerogenic Extrathymic Aire-Expressing Populations with Unique Homology to Thymic Epithelium 95%
Similar papers in this journal
- Identification of B cell subsets based on antigen receptor sequences using deep learning 96%
- Precision engineering of an anti-HLA-A2 chimeric antigen receptor in regulatory T cells for transplant immune tolerance 95%
- A single-cell atlas of lymphocyte adaptive immune repertoires and transcriptomes reveals age-related differences in convalescent COVID-19 patients 95%
Similar papers in this journal
- TCR meta-clonotypes for biomarker discovery with tcrdist3: identification of public, HLA-restricted SARS-CoV-2 associated TCR features 96%
- The T Cell Receptor beta Chain Repertoire of Tumor Infiltrating Lymphocytes Improves Neoantigen Prediction and Prioritization 95%
- Transposable elements regulate thymus development and function 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.