Modeling recognition between T-cell receptors (TCRs) and peptide-MHC (pMHC) complexes is a fundamental challenge in computational immunology, constrained by sparse paired interaction data relative to abundant unpaired sequences. We introduce DecoderTCR, a masked language model framework that addresses this through two contributions: (1) a compositional continual pre-training curriculum that learns component representations from marginal data before refining cross-chain dependencies from limited pairs, and (2) Iterative Entropy-Guided Refinement (IEGR), a non-autoregressive decoding algorithm that resolves high-confidence positions first to provide context for uncertain regions. On held-out benchmarks, DecoderTCR achieves 0.96 AUROC for zero-shot pMHC binding prediction and 0.76 AUROC for epitope-specific TCR recognition, approaching supervised baselines without epitope-specific training. Learned representations recover structural contacts without coordinate supervision, and generated sequences exhibit realistic recombination statistics. Experimental validation reveals a prediction-generation gap: strong discrimination does not yet yield reliable generation, highlighting an open challenge for the field.
DecoderTCR: Compositional Pretraining and Entropy-Guided Decoding for TCR-pMHC Interactions.
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作者:Lai Boqiao, Englund Melissa, Bharanikumar Ramit, Nocedal Isabel, Davariashtiyani Ali, Perera Jason, Khan Aly A
| 期刊: | bioRxiv | 影响因子: | 0.000 |
| 时间: | 2026 | 起止号: | 2026 Feb 6 |
| doi: | 10.64898/2026.02.04.703820 | ||
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