Training of epitope-TCR prediction models with healthy donor-derived cancer-specific T cells

Methods Cell Biol. 2024:183:143-160. doi: 10.1016/bs.mcb.2023.08.001. Epub 2023 Sep 15.

Abstract

Discovery of epitope-specific T-cell receptors (TCRs) for cancer therapies is a time consuming and expensive procedure that usually requires a large amount of patient cells. To maximize information from and minimize the need of precious samples in cancer research, prediction models have been developed to identify in silico epitope-specific TCRs. In this chapter, we provide a step-by-step protocol to train a prediction model using the user-friendly TCRex webtool for the nearly universal tumor-associated antigen Wilms' tumor 1 (WT1)-specific TCR repertoire. WT1 is a self-antigen overexpressed in numerous solid and hematological malignancies with a high clinical relevance. Training of computational models starts from a list of known epitope-specific TCRs which is often not available for new cancer epitopes. Therefore, we describe a workflow to assemble a training data set consisting of TCR sequences obtained from WT137-45-reactive CD8 T cell clones expanded and sorted from healthy donor peripheral blood mononuclear cells.

Keywords: Epitope specificity; Machine learning; T cell expansion; T-cell receptor; TCR repertoire; Wilms' tumor 1.

MeSH terms

  • CD8-Positive T-Lymphocytes
  • Epitopes
  • Humans
  • Leukocytes, Mononuclear*
  • Neoplasms*
  • Receptors, Antigen, T-Cell / genetics

Substances

  • Epitopes
  • Receptors, Antigen, T-Cell