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BioSyngen is developing multiple T-cell immunotherapies with the aim to address a wide range of malignancies.

Biosyngen Presents Pioneering“Conditional Activation + Armor Enhancement” SUPER-T technology at ESMO 2024

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Barcelona, Spain – September 13-17, 2024 – The highly anticipated 2024 European Society for Medical Oncology (ESMO) Annual Congress has taken place in Barcelona, Spain. As one of the most influential annual gatherings in oncology, this congress brings together leading cancer experts and researchers from around the globe, showcasing the latest advancements in the field and providing high-quality educational and networking opportunities for oncology professionals.

 

Biosyngen, an innovative biotechnology company specializing in immune cell therapies, is presenting its groundbreaking “Conditional Activation + Armor Enhancement” T-cell technology at this year's ESMO conference.

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Abstract Title

Antitumor Efficacy and Safety of “Conditional Activation + Armor Enhancement” CAR-T Cells for Gastrointestinal Tumor

 

Title No.

1033P

 

Gastrointestinal tumors have been found to exhibit significantly elevated levels of tumor-associated antigens (TAAs) compared to normal tissues, presenting potential targets for immune cell therapies. However, these TAAs are also expressed at certain levels in normal tissues, which poses a challenge for CAR-T cell therapies. Current CAR-T cells often fail to distinguish between tumor and normal tissues, leading to damage to normal organs and adverse clinical reactions. This on-target off-tumor toxicity not only raises safety concerns in clinical treatment but also limits dosage and efficacy enhancement.

 

To overcome this technical challenge and balance safety with efficacy in solid tumor immune cell therapies, Biosyngen has developed the SUPER-T™ T cell safety optimization platform and created the Conditional Activation CAR-T cell BTRP003L. This technology allows CAR-T cells to activate only under hypoxic conditions typical of the tumor microenvironment (0.3% ~ 2.0% O2), while remaining inactive in normal tissues (3.4% ~ 6.8% O2). Remarkably, this approach not only regulates CAR-T cell activation levels under different conditions effectively but also enhances their antitumor capabilities (Figure 1). Further advancements include the co-expression of a TGFβRII dominant-negative mutant, resulting in the “Conditional Activation + Armor Enhancement” CAR-T cell BTRP011L, which shows improved efficacy and in vivo persistence at lower doses (Figure 2). Toxicology studies using the SUPER-T™ platform showed no weight loss or other adverse effects in mice injected with BTRP003L or BTRP011L, demonstrating robust safety (Figure 3).

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Figure 1: Conditional activation CAR-T cells exhibit prolonged tumor control in animal models.

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Figure 2: “Conditional Activation + Armor Enhancement” CAR-T cells show superior tumor control in animal models.

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Figure 3: “Conditional Activation + Armor Enhancement” CAR-T cells demonstrate reliable safety in toxicology models.

 

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About Biosyngen’s Innovative Technology Platforms

Identifier™ Platform: A drug discovery platform providing a solid foundation for the discovery of antigens, antibodies, and TCRs. With a database of hundreds of TCRs and tumor proteins, this platform supports rapid screening and optimization, identifying the most unique and suitable tumor antigens. This platform serves as a pioneer. As the ancients said, "Before troops are mobilized, provisions must be in place," which is precisely why the Identifier™ platform exists — to obtain the necessary "provisions" more rapidly.

 

MSE-T™ Platform: A T-cell function enhancement platform that improves the ability of immune cells to recognize tumor-specific antigens and overcome the immunosuppressive tumor microenvironment, thereby more effectively in treating difficult-to-treat solid tumors.

 

SUPER-T™ Platform: A T-cell safety optimization platform that enhances the safety of immunotherapy through conditional activation in the tumor microenvironment. This platform ensures maximum safety for the drug.