Hu-Immune™ Platform: Humanized Immune System Mouse Models

huPBMC-T Mice

Inquiry

Alfa Cytology's huPBMC-T mice is an innovative platform specifically designed to accelerate T-cell immunotherapy development. By reconstituting a functional human T-cell immune system, this model provides drug developers with a highly reliable preclinical evaluation tool. Whether for CAR-T cell therapy, immune checkpoint inhibitors, or bispecific antibodies, the huPBMC-T model can provide highly clinically predictive efficacy data in a short period. We not only provide high-quality animal models but also offer end-to-end professional services from experimental design and model establishment to data analysis.

Introduction tohuPBMC-T Mice

The huPBMC-T model establishes a robust humanized immune system by engrafting healthy donor-derived PBMCs into immunodeficient NCG or NSG mice, leading to a predominant reconstruction of functional human T cells.

  • The optimized protocol enables experiments to commence within a remarkably short timeframe of 10-14 days.
  • Hu-Immune™ platform achieves a consistent model success rate exceeding 90%. A rigorous QC system ensures high data reliability by maintaining the hCD45+ cell coefficient of variation below 50%.
  • The model provides a stable experimental window of over 3 weeks, which is critical for obtaining meaningful pharmacodynamic data and has been demonstrated to support effective T cell infiltration into tumor tissues.

Compared to the traditional model,the HuPBMC-T model significantly improves the success rate and stability of model construction.Fig.1 Compared to the traditional model, the HuPBMC-T model significantly improves the success rate and stability of model construction.

Significant human immune cell infiltration in the humanized immune system of xenografted tumors.Fig.2 Significant human immune cell infiltration in the humanized immune system of xenografted tumors.

Advantages of huPBMC-T Mice

Excellent Model Stability

Modeling success rate up to 90%, significantly better than the 35-50% success rate of conventional models.

Adequate Experimental Window

Guarantees a stable experimental period of over 3 weeks, supporting complete pharmacodynamic evaluation.

Excellent Data Consistency

hCD45+ cell coefficient of variation controlled below 50%, ensuring reliable and reproducible experimental results.

Broad Tumor Model Compatibility

Validated for use with over 400 CDX models and over 400 PDX models.

Applications of huPBMC-T Mice

Cellular Immunotherapy Evaluation

Safety and efficacy evaluation of cellular therapies including CAR-T, TCR-T, and TIL.

Immune Checkpoint Inhibitor Research

Monotherapy or combination therapy research on checkpoint inhibitors including PD-1/PD-L1, CTLA-4, and 4-1BB.

Tumor Microenvironment Modulation Strategies

Drug development and mechanism research on tumor microenvironment targets including TGF-β and Treg.

Case Study

Case 1: Evaluation of Treg-Modulating and Cytokine Therapies in huPBMC-T Humanized Model

Overview

Assess antitumor activity and immune reconstitution in huPBMC-T humanized NCG model using a Treg-modulating anti-CD25 antibody and a cytokine regimen.

Study Information

  • Humanized Model: huPBMC-T on NCG strain
  • Tumor Model: KAPPAS299 human lymphoma cell line
  • Treatment: Novel Treg-targeting immunomodulator

Results

  • Effective Treg Modulation: The test drug effectively modulated the intratumoral Treg population, reducing this key immunosuppressive cell type within the tumor microenvironment.
  • Promoted Anti-tumor Activity: Modulation of Tregs was associated with promoted anti-tumor activity and tumor growth inhibition.
  • Model Validation: The study validated the huPBMC-T model's capability to support the evaluation of therapies targeting specific immune cell populations within a complex humanized TIME.

Antitumor efficacy and human immune reconstitution in huPBMC-T humanized NCG model.

Antitumor efficacy and human immune reconstitution in huPBMC-T humanized NCG model.

Antitumor efficacy and human immune reconstitution in huPBMC-T humanized NCG model.

Fig. 3 Anti-tumor efficacy and human immune reconstitution in huPBMC-T humanized NCG model.

Case 2: PD-1 Inhibitor and TGF-β Target Study in huPBMC-T Humanized Model

Overview

This study aimed to assess the efficacy of a PD-1 inhibitor, both as monotherapy and in combination with a TGF-β signaling inhibitor, showcasing the model's power in evaluating combination immunotherapy strategies.

Study Information

  • Humanized Model: huPBMC-T on NCG strain
  • Tumor Model: Jeko-1 human mantle cell lymphoma
  • Treatment: PD-1 inhibitor, TGF-β signaling inhibitor, and their combination

Results

  • Clinical-like Response: The model successfully recapitulated a clinical-like response to PD-1 blockade, confirming its relevance for checkpoint inhibitor evaluation.
  • Synergistic Effect: The combination of PD-1 and TGF-β inhibition clearly revealed a synergistic effect, leading to enhanced tumor growth suppression compared to either agent alone.
  • Platform for Combination Therapy: The results highlight the model's power in deconvoluting complex interactions between immunotherapeutic agents and supporting the development of combination strategies.

Anti-tumor efficacy of PD-1, GARP-ab, and their combination in huPBMC-T humanized NCG model.Fig. 4 Anti-tumor efficacy of PD-1, GARP-ab, and their combination in huPBMC-T humanized NCG model.

The huPBMC-T model is the ideal preclinical evaluation platform for your T-cell immunotherapy development. Alfa Cytology's Hu-Immune™ platform provides end-to-end professional services from model establishment to data analysis. Contact our scientific team now for customized solutions.

For research use only.

Online Inquiry