T-SCAPE: T cell immunogenicity scoring via cross-domain aided predictive engine
T cell immunogenicity, the ability of peptide fragments to elicit T cell responses, is a critical determinant of the safety and efficacy of protein therapeutics and vaccines. While deep learning shows promise for in silico prediction, the scarcity of comprehensive immunogenicity data is a major challenge. We present T cell immunogenicity scoring via cross-domain aided predictive engine (T-SCAPE), a novel multidomain deep learning framework that leverages adversarial domain adaptation to integrate diverse immunologically relevant data sources, including major histocompatibility complex (MHC) presentation, peptide-MHC (pMHC) binding affinity, T cell receptor-pMHC interaction, source organism information, and T cell activation. Validated through rigorous leakage-controlled benchmarks, T-SCAPE demonstrates exceptional performance in predicting T cell activation for specific peptide-MHC pairs. It also accurately predicts the antidrug antibody-inducing potential of therapeutic antibodies without requiring MHC inputs. This success is attributed to T-SCAPE's biologically grounded and data-driven multidomain pretraining. Its consistent and robust performance highlights its potential to advance the development of safer and more effective vaccines and protein therapeutics.
Authors
- Chaok Seok (ORCID: https://orcid.org/0000-0002-1419-9888)
- Nam‐Hyuk Cho (ORCID: https://orcid.org/0000-0003-3673-6397)
- Jinsung Noh (ORCID: https://orcid.org/0000-0002-7167-8113)
- Nuri Jung (ORCID: https://orcid.org/0000-0002-4596-1257)
- Jeonghyeon Kim (ORCID: https://orcid.org/0009-0001-4468-5035)
- J.Y. Lee (ORCID: https://orcid.org/0000-0002-5802-7180)
Institutions
- Seoul National University (KR)
- New Generation University College (ET)
Publication Details
- Journal
- Science Advances
- Published
- 2025-12-05
- DOI
- https://doi.org/10.1126/sciadv.adz8759
- Citations
- 2
- Primary Topic
- vaccines and immunoinformatics approaches
- Type
- article
- Field-Weighted Citation Impact
- 1.61