HLAIIPred: cross-attention mechanism for modeling the interaction of HLA class II molecules with peptides.

Journal: Communications biology
Published Date:

Abstract

We introduce HLAIIPred, a deep learning model to predict peptides presented by class II human leukocyte antigens (HLAII) on the surface of antigen presenting cells. HLAIIPred is trained using a Transformer-based neural network and a dataset comprising of HLAII-presented peptides identified by mass spectrometry. In addition to predicting peptide presentation, the model can also provide important insights into peptide-HLAII interactions by identifying core peptide residues that form such interactions. We evaluate the performance of HLAIIPred on three different tasks, peptide presentation in monoallelic samples, immunogenicity prediction of therapeutic antibodies, and neoantigen prioritization for cancer immunotherapy. Additionally, we created a dataset of biotherapeutics HLAII peptides presented by human dendritic cells. This data is used to develop screening strategies to predict the unwanted immunogenic segments of therapeutic antibodies by HLAII presentation models. HLAIIPred demonstrates superior or equivalent performance when compared to the latest models across all evaluated benchmark datasets. We achieve a 16% increase in prediction of presented peptides compared to the second-best model on a set of unseen peptides presented by less frequent alleles. The model improves clinical immunogenicity prediction, identifies epitopes in therapeutic antibodies and prioritize neoantigens with high accuracy.

Authors

  • Mojtaba Haghighatlari
    Pitzer Center for Theoretical Chemistry, Department of Chemistry, University of California, Berkeley, California 94720, United States.
  • Nicholas Marze
    Biomedicine Design, Pfizer Research and Development, Cambridge, MA, USA.
  • Robert Seward
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
  • Andrew Ciarla
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
  • Rachel Hindin
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
  • Jennifer Calderini
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
  • Benjamin Keenan
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
  • Santosh Dhule
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
  • Sarah Hall-Swan
    Machine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA, USA.
  • Timothy P Hickling
    Biomedicine Design, Pfizer Research and Development, Cambridge, MA, USA.
  • Eric Bennett
    Biomedicine Design, Pfizer Research and Development, Cambridge, MA, USA.
  • Brajesh Rai
    Machine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA, USA.
  • Sophie Tourdot
    Pharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.