NeoPAIR-T: Functional Mapping of Neoantigen-TCR Pairs Using a CRISPR-Engineered Jurkat Reporter System

Koji Nagaoka1, Yukari Kobayashi1, Kazuhiro Kakimi1

  • 1Department of Immunology, Kindai University Faculty of Medicine, Sakai 590-0197, Osaka, Japan.

Cells
|November 26, 2025
PubMed

Insights

This study introduces NeoPAIR-T, a new assay for identifying functional neoantigen-T cell receptor (TCR) pairs. This method streamlines personalized cancer immunotherapies by efficiently screening tumor-reactive TCRs for vaccine and TCR-T cell applications.

Area of Science:

  • Immunology
  • Oncology
  • Biotechnology

Background:

  • Personalized immunotherapies targeting neoantigens show promise but face challenges in identifying true neoantigens and cognate T cell receptors (TCRs).
  • Computational predictions of neoantigen peptides are often uncertain, and most tumor-infiltrating lymphocytes are bystanders, necessitating functional validation.
  • Current methods require extensive peptide synthesis and lack efficiency in screening neoantigen-TCR pairs.

Purpose of the Study:

  • To develop a functional assay, NeoPAIR-T (Neoantigen-TCR Pairing Assay using reporter T cells), for efficient screening and identification of functional neoantigen-TCR pairs.
  • To overcome limitations in neoantigen prediction and TCR reactivity assessment for personalized cancer immunotherapy.
  • To provide a streamlined approach for identifying neoantigen-TCR pairs for vaccine and TCR-T cell therapies.

Main Methods:

  • Developed NeoPAIR-T, a co-culture assay using engineered TCR-T reporter cells (Jurkat-derived with luciferase/eGFP dual reporter) and autologous antigen-presenting cells (APCs) transfected with tandem minigenes (TMGs) encoding predicted neoantigens.
  • Incorporated TCRα-knockout with targeted TCRβ knock-in to prevent TCR mispairing and enable parallel testing of multiple reporter T cell clones.
  • Applied whole-exome and RNA sequencing to lung cancer samples to predict neoantigens, assembled into TMGs, and used single-cell RNA/TCR sequencing to identify TCR clonotypes for reporter T cell engineering.

Main Results:

  • NeoPAIR-T successfully identified two functional neoantigen-TCR pairs from lung cancer samples.
  • The assay demonstrated high efficiency by testing eight TCR clonotypes in parallel against TMG-expressing APCs.
  • Functional pairs were validated by peptide assays, showing high affinity (EC50: 10^-9.2 to 10^-6.7 M).

Conclusions:

  • NeoPAIR-T is an effective and streamlined functional assay for identifying neoantigen-TCR pairs.
  • This assay overcomes key challenges in neoantigen and TCR identification, facilitating personalized cancer immunotherapies.
  • NeoPAIR-T has significant implications for the development of novel cancer vaccines and TCR-T cell therapies.

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