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pMMLV-CAR CD20 (Leu16) h(BBζ) (CAR-MV-01LX250)

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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.

Recombinant Moloney murine leukemia virus (MMLV) retroviral vectors serve as efficient viral vector tools for introducing genes permanently into a wide variety of dividing cells, and provide an alternative to modify primary T cells. Creative biolabs has developed retroviral CAR vector pMMLV CD20 (Leu16) h(BBζ), which is constructed for the engineering of T cells to target human CD20. The T cells are genetically modified through transduction with a retroviral vector expressing scFv of anti-CD20 antibody linked to CD137 (4-1BB) and CD3-zeta signaling domains. And the vector product was designed for the treatment of Acute lymphoblastic leukemia (ALL).

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Details

  • Target
  • CD20
  • Targeting Cell Type
  • T cell
  • Targeting Diseases
  • Acute lymphoblastic leukemia (ALL)
  • Generation
  • Second
  • Vector Name
  • pMMLV
  • Vector Length
  • ~6kb
  • Vector Type
  • Recombinant Moloney murine leukemia virus (MMLV) retroviral vector
  • Receptor Construction
  • scFv-41BB-CD3ζ
  • Discription of Signaling Cassetes
  • 41BB
    CD137 (also known as 4-1BB) is a surface co-stimulatory glycoprotein originally described as present on activated T lymphocytes, which belongs to the tumor necrosis factor (TNF) receptor superfamily. It is expressed mainly on activated CD4+ and CD8+ T cells, and binds to a high-affinity ligand (4-1BBL) expressed on several antigen-presenting cells such as macrophages and activated B cells. On the basis of preclinical observation, this molecule can promote the persistence of antigen-specific and antigennonspecific chimeric antigen receptor T-cells to significantly increases antitumor activity.
    CD3ζ
    CD3ζ, also known as T-cell receptor zeta, which together with T-cell receptor and CD3γ, δ, ε chain, forms the TCR-CD3 complex. ζ was expressed independently from the complex. The zeta chain plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. CD3-zeta, which contains 3 ITAMs, is the most commonly used endodomain component of CARs. It transmits an activation signal to the T cell after antigen is bound. CD3-zeta may not provide a fully competent activation signal and additional co-stimulatory signaling is needed. For example, chimeric 4-1BB and OX40 can be used with CD3-zeta to transmit a proliferative/survival signal, or all three can be used together.

Target

  • Clone
  • Leu16
  • Host
  • Mouse
  • Target Species
  • Human
  • Gene Name
  • membrane spanning 4-domains A1
  • Synonyms
  • B1; S7; Bp35; CD20; CVID5; MS4A2; LEU-16; BA0185

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  • Published Data
Complete CAR data FuncS

Fig.1 Specific cytotoxicity assay.

CAR Construction : leu-16-CD28-41BB-CD3ζ Latest CAR Construction

Fig.1 Specific cytotoxicity assay.

CD20-specific cytotoxicity of G418-selected autologous patient T cells was assessed with 5-hour chromium-release assays using the following 51Cr-labeled target cells: Granta cells (MCL), Daudi cells (Burkitt NHL), EL4 cells transfected to express CD20, or the parental EL4 cell line lacking CD20 expression.

Till, B. G., Jensen, M. C., Wang, J., Qian, X., Gopal, A. K., Maloney, D. G., ... & Press, O. W. (2012). CD20-specific adoptive immunotherapy for lymphoma using a chimeric antigen receptor with both CD28 and 4-1BB domains: pilot clinical trial results. Blood, The Journal of the American Society of Hematology, 119(17), 3940-3950.

Complete CAR data FuncS

Fig.2 Change in tumor volume over time.

CAR Construction : leu-16-CD28-41BB-CD3ζ Latest CAR Construction

Fig.2 Change in tumor volume over time.

The sum of the products of the diameters of the 7 largest lymph nodes seen on the baseline and 1-, 6-, and 12-month CT scans.

Till, B. G., Jensen, M. C., Wang, J., Qian, X., Gopal, A. K., Maloney, D. G., ... & Press, O. W. (2012). CD20-specific adoptive immunotherapy for lymphoma using a chimeric antigen receptor with both CD28 and 4-1BB domains: pilot clinical trial results. Blood, The Journal of the American Society of Hematology, 119(17), 3940-3950.

Complete CAR data FuncS

Fig.3 Immune responses against modified cells.

CAR Construction : leu-16-CD28-41BB-CD3ζ Latest CAR Construction

Fig.3 Immune responses against modified cells.

An ELISA testing Ab binding to the murine Leu16 from which the αCD20-28-BB-ζ scFv is derived (Figure A); and a flow cytometry-based assay using HEK-293 cells transfected with the L29.19.1 plasmid (Figure B). No convincing evidence indicated humoral immune responses to the infused cells. Cellular immune responses were tested (Figure C). No evidence indicated cellular immune responses against the modified T cells

Till, B. G., Jensen, M. C., Wang, J., Qian, X., Gopal, A. K., Maloney, D. G., ... & Press, O. W. (2012). CD20-specific adoptive immunotherapy for lymphoma using a chimeric antigen receptor with both CD28 and 4-1BB domains: pilot clinical trial results. Blood, The Journal of the American Society of Hematology, 119(17), 3940-3950.

Complete CAR data FuncS

Fig.4 Anti-tumor effect of transduced T cells in vivo.

CAR Construction : leu-16-CD28-41BB-CD3ζ Latest CAR Construction

Fig.4 Anti-tumor effect of transduced T cells in vivo.

NSG mice were inoculated i.v. with Raji-ffLuc tumors followed 2 days later by infusion of 5 × 106^6 CD20-targeted CAR+T cells, with or without i.p. injection of 30 mg i.v immune globulin (IVIG) per mouse 4 hours prior to T cell infusion. Survival curves is compared using a log-rank (Mantel-Cox) test.

Lee, S. Y., Olsen, P., Lee, D. H., Kenoyer, A. L., Budde, L. E., O’Steen, S., ... & Till, B. G. (2018). Preclinical optimization of a CD20-specific chimeric antigen receptor vector and culture conditions. Journal of immunotherapy (Hagerstown, Md.: 1997), 41(1), 19.

Complete CAR data BI

Fig.5 Anti-tumor effect of transduced T cells in vivo.

CAR Construction : leu-16-CD28-CD3ζ Latest CAR Construction

Fig.5 Anti-tumor effect of transduced T cells in vivo.

NSG mice were injected intravenously (i.v.) with 0.5 × 10^6 firefly-luciferase-expressing Raji cells 6 days prior to treatment with 5 × 10^6 CD8+ CD20-targeting CAR-T cells delivered i.v. Tumor progression was monitored by bioluminescence imaging. Black dotted line in the right data box denotes day 12 post T-cell injection, the time at which the CAR-T cell group began to rapidly lose tumor control.

Chen, X., Khericha, M., Lakhani, A., Meng, X., Salvestrini, E., Chen, L. C., ... & Chen, Y. Y. (2020). Rational tuning of CAR tonic signaling yields superior T-cell therapy for cancer. bioRxiv.

Complete CAR data ELISA

Fig.6 Evualution of tumor activation and exhaustion.

CAR Construction : leu-16-CD28-CD3ζ Latest CAR Construction

Fig.6 Evualution of tumor activation and exhaustion.

Activation and exhaustion maker expression on CAR+ T cells were evaluated 11 days post Dynabead removal, without CD20 antigen stimulation.

Chen, X., Khericha, M., Lakhani, A., Meng, X., Salvestrini, E., Chen, L. C., ... & Chen, Y. Y. (2020). Rational tuning of CAR tonic signaling yields superior T-cell therapy for cancer. bioRxiv.

CAR scFv data FACS

Fig.7 Competition cell-binding assay.

CAR Construction : Latest CAR Construction

Fig.7 Competition cell-binding assay.

Binding to CD20-positive Daudi cells was evaluated by competition of parental Leu-16 or scFv-Fc with FITC-Leu-16 by FACS. (A) GS18/C233S scFv-Fc. (B) GS8/nat scFv-Fc.

Wu A M, Tan G J, Sherman M A, et al. Multimerization of a chimeric anti-CD20 single-chain Fv-Fc fusion protein is mediated through variable domain exchange[J]. Protein engineering, 2001, 14(12): 1025-1033.

More Published Data More Published Data

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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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