Our bespoke CAR designs meticulously optimize all components, ensuring optimal specificity, potency, and persistence for your cancer or viral target.
Are you currently facing challenges in developing effective immunotherapies for difficult-to-treat cancers or persistent viral infections? Our other cancer or viral infection-specific CAR construction service helps you accelerate therapeutic development and achieve highly specific, potent cellular therapies through advanced CAR design and engineering techniques.
Besides the main categories of cancer, such as Leukemia, Lymphoma, Carcinoma, Sarcoma, Blastoma, and Germ cell tumors, Creative Biolabs also provides world-class CAR products targeting other cancers, including glioma, tumor vasculature, and viral infections. Our many years of experience and the most advanced techniques enable us to offer you the first-class products according to your specific requirements. Tumor regression mechanisms involve targeting both tumor antigen and tumor vasculature, which helps the tumor grow. Our skilled scientists and technicians have successfully constructed CARs targeting tumor vasculature antigens.
Fig.1 Schematic of lymphodepletion before CAR T infusion on tumor cells and the immune microenvironment.1
Creative Biolabs' other cancer or viral infection-specific CAR construction service delivers precisely engineered CAR constructs tailored to your unique therapeutic targets. We provide comprehensive solutions for developing novel CARs against a wide range of "other" cancers, including various gliomas and tumor vasculature antigens, as well as persistent viral infections. Our service is designed to overcome the inherent challenges of these diseases, such as antigen heterogeneity, immunosuppressive microenvironments, and viral latency, by integrating advanced CAR designs that enhance specificity, persistence, and anti-tumor/anti-viral efficacy.
Creative Biolabs has successfully constructed different types of bispecific chimeric antigen receptors (called Tan CAR) modified T cells approaches, which make genetically engineered T cells recognize and target both cancer antigens and latent-virus antigens (such as from attack cytomegalovirus (CMV), EBV, or adenovirus). In addition to the multiple cancer antigens, elite scientists from Creative Biolabs have successfully placed bispecific CAR targeting cancer antigen grafted with latent-virus antigen in T cells to recognize and attack CMV or EBV, or adenovirus, which makes genetically engineered T cells work better to react to the virus as well as to cancer cells.
Our bespoke CAR designs meticulously optimize all components, ensuring optimal specificity, potency, and persistence for your cancer or viral target.
We offer advanced CAR architectures, including multi-antigen targeting, externally controllable CARs to overcome immunosuppressive microenvironments.
Our capabilities extend to engineering various immune cell types, including CAR-T, CAR-NK, and CAR-Macrophage cells, each optimized for their unique therapeutic advantages.
Our seamless, one-stop service, from target identification to final deliverables, ensures efficient project progression with dedicated scientific support.
Q1: Can Creative Biolabs develop CARs specifically for viral infections, and how do they work?
A1: Yes, we construct CARs to target latent viral antigens. These CARs enable engineered T cells to attack virally infected cells and, in some cases, associated cancer cells, offering a dual therapeutic benefit.
Q2: How does Creative Biolabs address the challenges of solid tumors, such as the immunosuppressive tumor microenvironment?
A2: We employ advanced CAR designs to overcome the hostile tumor microenvironment. This includes developing "armored" CARs that secrete beneficial cytokines or express dominant-negative receptors to neutralize inhibitory signals. We also engineer CARs to enhance T-cell or NK cell trafficking and persistence within the tumor, and for CAR-macrophages, we focus on strategies to degrade the fibrotic extracellular matrix.
Q3: What information or materials do I need to provide to start a project with Creative Biolabs?
A3: To initiate your project, we typically require target antigen information (sequence/identifier, expression profile), any available antibody/ligand sequences for the binding domain, and your specific project goals/CAR design specifications. Our scientific team can guide you if you lack full details.
Creative Biolabs' other cancer or viral infection-specific CAR construction service offers distinct advantages that accelerate your research and development. We leverage advanced CAR design principles, including affinity-tuned scFvs, optimized spacer and transmembrane domains, and tailored co-stimulatory profiles, to engineer CARs with superior specificity, reduced off-target toxicity, and enhanced persistence.
"We utilized Creative Biolabs for Viral Infection Specific CAR Construction targeting CMV. The IL-21 armored CAR-NK cells they engineered showed remarkably enhanced persistence and potent cytotoxic activity against virally infected cells in our in vivo models, outperforming our previous designs. The detailed metabolic pathway analysis they provided was invaluable." - Prof. Jn Sth
"Creative Biolabs' comprehensive workflow for CAR Construction saved us invaluable time and resources. Their expertise in vector selection and rigorous functional validation meant we received high-quality, ready-to-use CAR constructs and cells, accelerating our project timeline by several months. Their team was highly responsive and professional throughout the entire process." - Dr. An Wg
Ready to advance your next-generation CAR therapy project? Our expert team is eager to discuss your specific requirements and provide tailored solutions.
For more information or to discuss your specific project, please reach out to our team.
Please note: We guarantee to offer you the best-in-class CARs products, which can undoubtedly satisfy various customers' needs. If you are unable to find the item of your choice, please don't hesitate to contact us at any time.
| Associated malignancy | Target antigen | Receptor type | Product |
|---|---|---|---|
| Brainstem glioma | EGFRvIII | scFv-CD28-41BB-CD3ζ | CAR-T-3-M315-2BZ |
| VHH-CD28-OX40-CD3ζ | XS-0323-LX997 | ||
| scFv-CD28-FcεRIγ | CAR-T-2-M315-2G | ||
| Optic nerve glioma | VEGFR-2 | VHH-ICOS-4-1BB-CD3ζ | XS-0323-LX629 |
| scFv-CD28-FcεRIγ | CAR-T-2-L341-2G | ||
| scFv-CD28-41BB-CD3ζ | CAR-T-3-L341-2BZ | ||
| Autoimmune arthritis | C2 | scFv-CD28-41BB-CD3ζ | CAR-T-3-M304-2BZ |
| CD37 | scFv-CD28-OX40-CD3ζ | CAR-T-3-L333-2XZ | |
| Pancreatic cancer | PSCA | scFv-CD28-41BB-CD3ζ | CAR-T-3-L347-2BZ |
| CLD18A2 | scFv-CD28-41BB-CD3ζ | CAR-LC200 | |
| Mesothelin | scFv-41BB-FKBP/41BB-FRB-CD3ζ | CAR-LC269 | |
| CEA | scFv-CD28-OX40-CD3ζ | CAR-MZ108 | |
| FR+ cancer | FITC | scFv-CD28-41BB-CD3ζ | CAR-T-3-L340-2XZ |
| Cancer | Biotin | mcAv/dcAv-FcεRIγ | CAR-T-1-M400-G |
| MUC1-expressing tumors | Tn-MUC1 | scFv-CD28-CD3ζ | CAR-LC128 |
| MUC1 | scFv-CD28-41BB-CD3ζ | CAR-LC251 | |
| CD4 ligands | CD4-10-gp120 scFv-CD28-CD3ζ | CAR-MZ248 |
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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