Exploring noise in TCR specificity data through supervised learning

Accurate prediction of T cell receptor (TCR) specificity can potentially accelerate development of novel immunotherapies, yet public databases used to train these models contain substantial label noise. This uncertainty complicates model evaluation and limits the reliability of predicted TCR-pMHC interactions. In this work, we present a simple supervised machine learning denoising scheme to identify low-quality labels in TCR specificity data. We evaluated the framework using the TCRvdb validation dataset and further corroborated it via structural modeling with AlphaFold 3. Here, our denoising approach successfully identified non-validated TCRs, achieving an average MCC of 0.47 for filtering non-validated examples while retaining high sensitivity for validated examples. Applying our denoising approach to the complete NetTCR training dataset, we observed that data associated with known noisy attributes were significantly enriched in the filtered subset. Furthermore, TCR-pMHC complexes identified as noise consistently produced lower AlphaFold 3 confidence scores, providing independent evidence of misannotation. Experimental validation of 30 selected TCRs further supported the approach, with 80% of TCRs predicted as noise failing to demonstrate functional reactivity. Our findings demonstrate that current performance metrics may be obscured by dataset inaccuracies and provide a method for refining training data in the absence of gold-standard benchmarks.