End-to-End TCR CRO | Allogeneic-HLA TCR Priming Technology
INFINITY-TCR specializes in end-to-end T cell receptor (TCR) research services. Our proprietary Allogeneic-HLA TCR Priming platform achieves 25–40× higher efficiency than conventional methods, completing the full TCR development cycle in as few as 9 days, empowering next-generation cancer immunotherapy.
Breaking through traditional TCR screening bottlenecks — our engineered APC system co-cultured with allogeneic PBMC achieves ultra-high efficiency TCR discovery, bridging the complete pathway from antigen target to functional TCR.
25–40× improvement over conventional methods. 24 parallel screening groups simultaneously, each covering 5–15 pHLA epitopes for large-scale high-throughput TCR capture.
25–40× Efficiency BoostFully optimized integrated workflow completes the entire TCR discovery cycle in as little as 9 days — from epitope screening to functional validation, dramatically shortening development timelines.
Fastest 9-Day CompletionProprietary T2/K562 engineered APC cells stably expressing target HLA and co-stimulatory molecules (B7, CD58), providing the optimal activation microenvironment for TCR Priming.
T2/K562 Engineered APCSingle-cell sorting combined with TCR VDJ sequencing to precisely obtain TCRα/β chain pairing information, ensuring accuracy and completeness of functional TCR discovery.
TCRα/β Precise PairingProprietary Jurkat-CD8-NFAT-GFP reporter cell line enables high-throughput TCR functional screening, precisely quantifying activation signals and assessing TCR activity multi-dimensionally.
HT Functional ScreeningLentiviral (>60%), retroviral (>80%), and mRNA-LNP (in development) delivery systems with digital PCR for precise copy number quantification, covering all gene delivery requirements.
>80% Transduction EfficiencyCovering the full TCR development lifecycle, our 7 specialized platforms work in synergy as a one-stop solution, driving innovation in TCR-T cell therapy.
24 parallel groups, each screening 5–15 pHLA epitopes. 25–40× efficiency boost. Fastest 9-day completion. Scalable high-throughput TCR capture.
Codon optimization, SS-TCR disulfide engineering, constant region enhancement, and Sc-TCR single-chain conversion — multi-strategy approach to improve TCR functionality and stability.
Lentiviral (>60%), retroviral (>80%) multi-vector system, mRNA-LNP in development. Digital PCR for precise expression level quantification.
T2/K562 engineered APC cells stably expressing target HLA and co-stimulatory molecules (B7, CD58) for optimal TCR Priming activation microenvironment.
Jurkat-CD8-NFAT-GFP reporter cell line enables high-throughput TCR functional screening, precise activation signal quantification, and multi-dimensional TCR activity assessment.
Mass spectrometry (MS), NetMHCpan prediction, QuickSwitch peptide exchange (>85% efficiency), and intracellular cytokine staining (ICS) — multi-technology combined validation.
Proprietary s-pHLA Tetramer/multimer with flow cytometry detection. Minimum detectable concentration 100pM, peak positivity rate 82.7%.
From antigen target to functional validation, our six-step standardized process covers the complete TCR development chain with QC checkpoints at each stage.
Bioinformatics prediction combined with QuickSwitch MFI quantitative validation. Validated targets: KRAS (HLA-A*02:01/03:01/11:01), WT1, NPM1.
Proprietary s-pHLA Tetramer/multimer synthesis; flow cytometry enrichment of antigen-specific T cells with positivity rate up to 82.7%.
Engineered T2/K562 APC co-cultured with allogeneic PBMC. 24 parallel groups, 25–40× efficiency improvement. TCR capture completed in as little as 9 days.
Precision single-cell sorting followed by high-throughput TCR VDJ sequencing to obtain complete TCRα/β chain pairing information with assured accuracy.
Codon optimization and SS-TCR engineering, combined with lentiviral (>60%) or retroviral (>80%) delivery. Digital PCR for precise copy number quantification.
ICS (IFNγ/IL-2), JK-TCR NFAT reporter assay, TCR-T killing assay, peptide titration (100pM–10μM), and off-target safety panel.
The following showcases real experimental data from the INFINITY-TCR platform, including 24-group parallel pHLA TCR screening flow cytometry data and 9-day/45-day TCR development workflow validation data.
Allogeneic-HLA TCR Priming platform, 24 groups simultaneously, peak Tetramer positivity rate 82.7%
IFNγ⁺CD8⁺ double-positive 16.3% (control 1.24%), IFNγ ICS functional validation results
INFINITY-TCR has completed in vitro validation for the following tumor-associated antigens, covering hematological malignancies, solid tumors, and virus-associated cancers. The target library is continuously expanding.
In-depth collaborations with leading medical institutions and research institutes, covering multi-cancer TCR development projects.
| # | Target | Indication | Status | Partners |
|---|---|---|---|---|
| 1 | WT1-126 | Blood tumors, Ovarian cancer | In vitro done · Patent published | Shanghai Ruijin Hospital |
| 2 | EBV | Nasopharyngeal, Gastric cancer | CTL screening in progress | Shanghai Ruijin Hospital |
| 3 | NPM1 | Blood tumors, Ovarian cancer | In vitro killing validated | Xi'an Jiaotong University |
| 4 | KRAS | Lung cancer, Pancreatic cancer | In vitro ongoing · Patent filed | Xi'an Jiaotong University |
| 5 | KRAS | Lung cancer, Pancreatic cancer | In vitro ongoing · Patent filed | Army Medical University |
| 6 | Transplant-reactive | Graft-versus-host disease | Testing | Zhejiang Univ. 2nd Affiliated Hospital |
| 7 | Undisclosed | Breast cancer | TCR functional validation | XJTU 2nd Affiliated Hospital |
| 8 | Multiple Targets | Cervical, Pancreatic cancer | In vitro killing validated | CAS SINH / Army Medical Univ. / China Pharmaceutical Univ. |
Deep strategic collaborations with leading universities, top-tier hospitals, national research institutes, and renowned enterprises worldwide.











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INFINITY-TCR (Shaanxi INFINITY-Biotechnology Co., Ltd.), founded in 2021, specializes in T cell receptor (TCR) discovery, screening, optimization, and validation, providing end-to-end CRO services for TCR-T cell therapy development.
Our proprietary Allogeneic-HLA TCR Priming core technology platform, through engineered APC cell lines co-cultured with allogeneic PBMC, achieves 25–40× higher TCR screening efficiency than conventional methods, completing the full TCR discovery workflow in as little as 9 days — effectively addressing the industry pain points of long development cycles and low efficiency.
Headquartered in Western Cloud Valley, Fengxi New Town, Xixian New Area, Shaanxi, the company has established strategic partnerships with leading 985/211 universities, top-tier hospitals, and internationally renowned research institutions. Services span oncology immunotherapy, infectious diseases, and autoimmune conditions.
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