By Drug Type

Cell Therapy

Biocytogen offers advanced platforms to support the development of diverse cell therapies, including CAR-T, CAR-Macrophages, CAR-NK, TILs, and TCR-T, providing both in vitro services and in vivo models for comprehensive research.

related resource

on this page

  • Introduction
  • Preclinical Capabilities for Cell Therapy Evaluation
  • Examples of Cell Therapy Preclinical Research

Publication

    Introduction

    Cell therapy involves transferring live cells into a patient to treat or cure diseases, using either the patient’s own cells (autologous) or donor cells (allogeneic). Immune cell therapies, especially CAR-T therapy, have revolutionized cancer treatment, achieving remarkable success in hematological malignancies. CAR-T cells are engineered T-cells modified to express chimeric antigen receptors that recognize and attack tumor antigens.

    Biocytogen offers advanced platforms to support the development of diverse cell therapies, including CAR-T, CAR-Macrophages, CAR-NK, TILs, and TCR-T, providing both in vitro services and in vivo models for comprehensive research. We have developed a series of immunodeficient mice and established CDX models along with immune reconstitution models to facilitate the evaluation of cell therapies.

    Preclinical Capabilities for Cell Therapy Evaluation
    Efficacy MOA Safety
    • In Vitro:
      • Cytotoxicity
      • Antigen-specific immune response
    • In Vivo:
      • CDX model
      • Immune reconstitution model
    • Immuno-profiling
    • Inflammatory factor analysis
    • CAR-T cell proliferation
    • Tissue distribution
    • PK
    • Blood routine/blood biochemistry
    • Pathological analysis of tissues and organs
    • CRS
    Examples of Cell Therapy Preclinical Research
    Case Study 1: CAR-T In Vivo Efficacy Study Using Raji Lymphoma CDX Tumor Model in B-NDG Mice

    A Raji lymphoma mouse model was established using B-NDG mice and the efficacy of anti-human CD47 antibodies were verified. B-luc-GFP Raji cells (5×105) were injected via tail vein of B-NDG mice. In vivo imaging systems (IVIS) was used to observe tumor growth. When the fluorescence intensity of the tumor reaches about 1×106 p/sec, the animals were divided into one control group and three treatment group (n=6). (A) Fluorescence intensity curve of tumor cells; (B) Body weight. The results showed that all three anti-human CD47 antibodies could significantly inhibit tumor growth. B-NDG mice is a powerful model for efficacy verification of anti-human CD47 antibodies. Values are expressed as mean ± SEM.