Related Experiment Video
Updated: Jan 10, 2026

CRISPR-Cas9-based Genome Engineering to Generate Jurkat Reporter Models for HIV-1 Infection with Selected Proviral Integration Sites
Published on: November 14, 2018
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.
Abstract:
Targeting mutation-derived neoantigens is a promising strategy for personalized immunotherapies. However, identifying true neoantigens and cognate T cell receptors (TCRs) remains challenging because computational prediction of neoantigen peptides is uncertain and most tumor-infiltrating lymphocytes are bystanders rather than tumor-reactive, necessitating functional validation. Here, we developed NeoPAIR-T (Neoantigen-TCR Pairing Assay using reporter T cells), a functional assay based on co-culture of TCR-T reporter cells and autologous antigen-presenting cells (APCs) to screen neoantigen-TCR pairs. Reporter T cells are Jurkat-derived cells engineered to express a luciferase/eGFP dual reporter, providing quantitative readouts of TCR activation, while APCs are immortalized autologous cells transfected with tandem minigenes (TMGs) encoding predicted neoantigens, bypassing peptide synthesis. NeoPAIR-T also includes TCRα-knockout with targeted knock-in of candidate TCRs at the TCRβ locus to prevent mispairing and enables parallel testing of multiple reporter T cell clones co-cultured with the same APCs for efficient identification of functional pairs. Using lung cancer samples, whole-exome and RNA sequencing predicted 63 candidate peptides assembled into three TMGs. Single-cell RNA/TCR sequencing identified eight TCR clonotypes, introduced into reporter T cells and tested in parallel. Co-culture with TMG-expressing APCs revealed two functional neoantigen-TCR pairs validated by peptide assays (EC50: 10-9.2-10-6.7 M). Collectively, NeoPAIR-T streamlines neoantigen-TCR identification for vaccine and TCR-T applications.
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.
More Related Videos
09:08Retroviral Transduction of Bone Marrow Progenitor Cells to Generate T-cell Receptor Retrogenic Mice
Published on: July 11, 2016
11:21Streamlined Single Cell TCR Isolation and Generation of Retroviral Vectors for In Vitro and In Vivo Expression of Human TCRs
Published on: September 10, 2017
Related Concept Videos
CRISPR
CRISPR and crRNAs
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
CRISPR/Cas9 Genome Editing