Designs dual/tandem CAR linkers and places TME-armoring transgenes in viral vectors to ensure balanced expression and minimize interference.
CAR-T Immunotherapy has achieved unprecedented response rates in B-cell malignancies and myeloma patients. While the application of CAR-T therapy in solid tumors is not satisfactory. The lack of cancer-specific antigens, poor trafficking and penetration of CAR-T cells into malignant sites, and tumor microenvironment have led to this challenge. Currently, a wide range of target antigens are being studied for solid tumor therapy, and the ErbB family serves as a rich source of antigen candidates based on a variety of characteristics including prevalence, immunogenicity, and specificity.
Fig.1 TME hurdles in CAR-T Cell Immune Therapy for Solid Tumors.1
To address these issues, Creative Biolabs provides a robust and effective pan-ErbB-targeted combination CAR-T cell engineering service to speed up global customers' solid research. The pan-ErbB-targeted combination CAR-T strategy incorporates the promiscuous ErbB ligand T1E, placed upstream of a second-generation CAR design with a chimeric cytokine receptor (CCR). This approach could simultaneously direct T-cells specifically target all ErbB1 homo- and heterodimers, the ErbB 2/3 heterodimer, and all ErbB4 homo- and heterodimers expressing tumor cells with potent cytotoxic activity against a broad range of tumor types, decreasing the risk of immune evasion. Powered by our years of experience in the CAR-T field, we provide a one-stop pan-ErbB-targeted combination CAR-T cell engineering service, including from CAR design & construction, to function validation to speed up customers' solid research.
Fig.2 Schematic of pan-ErbB-targeted combination CAR-T cell engineering.
To execute highly complex pan-ERBB and armored CAR-T engineering, we leverage a suite of validated, high-end technology platforms focused on precision and functional validation.
Designs dual/tandem CAR linkers and places TME-armoring transgenes in viral vectors to ensure balanced expression and minimize interference.
Optimized protocols and high-titer vectors enable efficient transduction and scalable production of homogeneous, functional T cells.
Multi-color flow cytometry plus assays for cytotoxicity under TME conditions, proliferation/persistence, and cytokine release confirm potency and durability.
The Creative Biolabs CellRapeutics™ workflow is a rigorous, phased process designed for maximum control and customization, ensuring a clinical-grade engineered product ready for preclinical testing.
Seek consultation today to receive detailed specs and personalize your service bundle.
Creative Biolabs designs TCR-ABR CARs combining antibody and TCR properties. Our services address restricted antigen recognition, providing broader targeting and improved tumor elimination capacity.
We engineer NKG2D-based CARs recognizing multiple ligands. Our services address tumor antigen escape, enhancing multi-target responses and broadening immune coverage for robust therapeutic outcomes.
Our team develops CAR-T cells targeting TRBCs for T cell malignancies. Services include construct design and testing, addressing clonal expansion, and supporting selective elimination of malignant T cells.
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Customized CAR Design & Construction
Competent research team |
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One-stop services
Reliable and reputable experiment systems |
Q1: What are the safety & challenges considerations for ErbB-targeted CARs?
A1: Several criteria need to be taken into account:
Fig.3 Work with Creative Biolabs.
If you are interested in our CellRapeutics™ pan-ErbB-targeted combination CAR-T cell engineering service, please don't hesitate to contact us. Our experienced scientists try our best to meet the most challenging requirements and deliver the best answer for global customer satisfaction.
Reference
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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.
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