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Pretrained models may fail to capture immunological sequences

  • Jiahao Ma (Co-first author)
  • , Hongzong Li (Co-first author)
  • , Jian-Dong Huang*
  • , Ye-Fan Hu*
  • , Yifan Chen*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Pretrained models, originally developed for vision and textual data, are not a panacea and may fail to fully represent the complexity of sequences in immunological tasks. In studying pretrained immunological sequence modules of a renowned immunogenicity prediction model, pMTnet, we observe that our carefully designed model removing (ablating) the pretrained T cell receptor (TCR) autoencoder in pMTnet can even improve the prediction accuracy. Furthermore, we note the TCR pretraining data, used by pretrained modules within pMTnet, dramatically deviates from a broader and more representative TCR repertoire. Such findings underscore the impacts of the blend of heterogeneous representations and distribution discrepancy in immunological sequences, which necessitate appropriate coordination of different pretrained models and representative databases.
Original languageEnglish
Number of pages17
JournalCommunications Biology
DOIs
Publication statusE-pub ahead of print - 20 Jul 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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