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Anti-NY-ESO-1 scFv h(CD28) CART, pCDCAR1 (CAR-T-1-M323-2)


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

The vector of anti-NY-ESO-1 chimeric antigen receptor (CAR) is constructed for the engineering of T cells to target human NY-ESO-1. The T cells are genetically modified through transduction with a lentiviral vector expressing scFv of anti-NY-ESO-1 antibody linked to CD28 signaling domains. And the vector product was designed for the treatment of metastatic melanoma and synovial cell sarcoma.

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Details

  • Target
  • NY-ESO-1
  • Targeting Cell Type
  • T cell
  • Targeting Diseases
  • Metastatic melanoma; synovial cell sarcoma
  • Generation
  • First
  • Vector Name
  • pCDCAR1
  • Vector Length
  • 8kb
  • Vector Type
  • Lentiviral
  • Receptor Construction
  • scFv-CD28
  • Discription of Signaling Cassetes
  • CD28
    CD28 (Cluster of Differentiation 28) is one of the proteins expressed on T cells that provide co-stimulatorysignals required for T cell activation and survival. CD28 is the receptor for CD80 (B7.1) and CD86 (B7.2) proteins which are expressed on antigen-presenting cells(APC). CD28 modulates the primary TCR/CD3ζ signal in a different fashion than the late costimulatory elements OX40 and 4-1BB. CD28 enhances the expression of downstream regulators that impact on T-cell proliferation, death, differentiation, and effector functions. CAR+ T cells containing the CD28 endodomain showed strikingly enhanced sustained T cell activation, growth, survival. And CD28 results in a brightly expressed, stable receptor as the transmembrane domain. Including CD28 costimulatory domains in CARs led to enhanced anti-malignancy efficacy.

Target

  • Clone
  • ES121
  • Host
  • Mouse
  • Target Species
  • Human
  • Gene Name
  • cancer/testis antigen 1B
  • Synonyms
  • CTAG; ESO1; CT6.1; CTAG1; LAGE-2; LAGE2B; NY-ESO-1

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  • Published Data
Complete CAR data ELISA

Fig.1 Antibody titration of positive clone mAb 2D2 via ELISA.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.1 Antibody titration of positive clone mAb 2D2 via ELISA.

Selection of scFvs specific for HLA-A2/NY-ESO-1 complex.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

Complete CAR data BLI

Fig.2 Binding affinity of mAb 2D2 to the HLA-A2/NY-ESO-1157-165.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.2 Binding affinity of mAb 2D2 to the HLA-A2/NY-ESO-1157-165.

The complex measured by the biolayer interferometry (BLI) on an Octet instrument.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

Complete CAR data FCM

Fig.3 Surface expression of CAR detected by HLA-A2/NY-ESO-1157-165 complex.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.3 Surface expression of CAR detected by HLA-A2/NY-ESO-1157-165 complex.

2D2-CAR T cells specifically recognize and lyze HLA-A2+/NY-ESO-1+cells in vitro.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

Complete CAR data Cyt

Fig.4 LDH cytotoxicity assay of 2D2-CAR T cells.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.4 LDH cytotoxicity assay of 2D2-CAR T cells.

2D2-CAR T cells were cocultured with T2 cells that were pulsed with 20µg/mL NY-ESO-1 or CMV peptide for 1 hour for 4 hours.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

Complete CAR data FuncS

Fig.5 2D2-CAR T cells impair tumor growth and prolong the survival of mice bearing triple-negative breast cancer in vivo.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.5 2D2-CAR T cells impair tumor growth and prolong the survival of mice bearing triple-negative breast cancer in vivo.

Representative survival analysis of MBA-MD-231-NY-ESO-1 bearing mice treated with 2D2-CAR T cells compared with the control group.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

Complete CAR data ELISA

Fig.6 IFN-γcytokine release measured by ELISA.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.6 IFN-γcytokine release measured by ELISA.

2D2-CAR T cells were cocultured with target cells with a 10:1 (E: T) ratio overnight.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

Complete CAR data IHC

Fig.7 Confocal imaging of mAb 2D2 staining in NY-ESO1157-165 peptide-pulsed HEK 293T.

CAR Construction : 2D2 scFv-BBζ Latest CAR Construction

Fig.7 Confocal imaging of mAb 2D2 staining in NY-ESO1157-165 peptide-pulsed HEK 293T.

HEK 293T cells were pulsed with 20µg/mL NY-ESO-1157-165 or CMV pp65495-503 peptide for 1 hour.

Liu, X., Xu, Y., Xiong, W., Yin, B., Huang, Y., Chu, J., ... & Wang, R. (2022). Development of a TCR-like antibody and chimeric antigen receptor against NY-ESO-1/HLA-A2 for cancer immunotherapy. Journal for immunotherapy of cancer, 10(3).

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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