Close

pCDCAR1 MUC1 h(4γ), T (CAR-T-2-M303-4G)


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

The vector of anti-MUC1 chimeric antigen receptor (CAR) is constructed for the engineering of T cells to target human MUC1. The T cells are genetically modified through transduction with a lentiviral vector expressing scFv of anti-MUC1 antibody linked to CD4 transmembrane domain and FcεRIγ signaling domains. And the vector product was designed for the treatment of MUC1-expressing tumors.

Specific Inquiry

  • Size:
  • Marker:
  • Form:
  Add to Cart

Details

  • Target
  • MUC1
  • Targeting Cell Type
  • T cell
  • Targeting Diseases
  • MUC1-expressing tumors
  • Generation
  • Second
  • Vector Name
  • pCDCAR1
  • Vector Length
  • 8kb
  • Vector Type
  • Lentiviral
  • Receptor Construction
  • scFv-CD4-FcεRIγ
  • Discription of Signaling Cassetes
  • CD4
    Cluster of Differentiation 4 (CD4) is a glycoprotein expressed on the surface of T helper cells, regulatory T cells, monocytes, macrophages and dendritic cells, and plays an important role in the development and activation of T cells. On T cells, CD4 is the co-receptor for the T cell receptor (TCR), and these two distinct structures recognize the Antigen-Major Histocompatibility Complex (MHC). CD4 signaling in CAR ensures specificity of the TCR-antigen interaction, prolongs the contact between the T cell and the antigen presenting cell and recruits the tyrosine kinase Lck, which is essential for T cell activation.
    FcεRIγ
    The high-affinity IgE receptor, also known as FcεRI, or Fc epsilon RI, is the high-affinity receptor for the Fc region of immunoglobulin E (IgE). FcεRI is a key molecule involved in allergic reactions. It is a tetramer composed of 1alpha, 1 beta, and 2 gamma chains. The gamma chains are also subunits of other Fc receptors. The scFv-based CARs engineered to contain a signaling domain from FcεRIγ have been shown to deliver a potent signal for T cell activation and function.

Target

  • Clone
  • SM3; HMFG2
  • Host
  • Mouse
  • Target Species
  • Human
  • Gene Name
  • mucin 1, cell surface associated
  • Synonyms
  • EMA; MCD; PEM; PUM; KL-6; MAM6; MCKD; PEMT; CD227; H23AG; MCKD1; MUC-1; ADMCKD; ADMCKD1; CA 15-3; MUC-1/X; MUC1/ZD; MUC-1/SEC; M3A1

Customize Your CAR Products

Cannot find the desired product? Don't worry, just try our online CAR and CAR cell customizing system, which offers full options to meet all unique needs, including but not limited to conventional or unconventional CAR constructs, as well as a variety of vectors and cells. The customization process can be completed with just a few simple clicks, please feel free to try it out.
CAR and CAR Cell Customizing System
  • Published Data
Complete CAR data Funcs

Fig.1 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with OME for 6hrs.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.1 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with OME for 6hrs.

Flow cytometry tested the lysis of different tumor cells by CAR-MUC1 T cells and GFP+ T cells, respectively. CAR-MUC1 T and GFP+ T cells were coculture with tumors cell from OME for 6 h.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.2 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with HN4 for 6hrs.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.2 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with HN4 for 6hrs.

Flow cytometry tested the lysis of different tumor cells by CAR-MUC1 T cells and GFP+ T cells, respectively. CAR-MUC1 T and GFP+ T cells were coculture with tumors cell from HN4 for 6 h.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.3 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with CAL33 for 6hrs.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.3 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with CAL33 for 6hrs.

Flow cytometry tested the lysis of different tumor cells by CAR-MUC1 T cells and GFP+ T cells, respectively. CAR-MUC1 T and GFP+ T cells were coculture with tumors cell from CAL33 for 6 h.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.4 IL-2 secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants after different E/T ratio were measured by ELISA assay.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.4 IL-2 secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants after different E/T ratio were measured by ELISA assay.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.5 IFN-γ secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants after different E/T ratio were measured by ELISA assay.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.5 IFN-γ secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants after different E/T ratio were measured by ELISA assay.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.6 TNF-α secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants after different E/T ratio were measured by ELISA assay.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.6 TNF-α secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants after different E/T ratio were measured by ELISA assay.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.7 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with tumor cell after exogenous addition of IL22 recombinant protein.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.7 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with tumor cell after exogenous addition of IL22 recombinant protein.

After 72 h of exogenous addition of IL22 recombinant protein, detected the killing of CAR-MUC1 T cells against OME cell line and different HNSCC cell lines in different E/T ratios.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.8 Cytokine secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants with different E/T ratio after exogenous addition of IL22 addition.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.8 Cytokine secretion of CAR-MUC1 T cells and GFP+ T cells in coculture supernatants with different E/T ratio after exogenous addition of IL22 addition.

After 72 hours of exogenous addition of IL22 recombinant protein, cytokine secretion in coculture supernatants after different E/T ratio were measured by ELISA assay.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.9 Microscopic observation of the ability of two different kinds of CAR-T cells and GFP+T cells to capture cells in 1:2 E/T ratio.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.9 Microscopic observation of the ability of two different kinds of CAR-T cells and GFP+T cells to capture cells in 1:2 E/T ratio.

In CAR-MUC1 T cells group, a little number of CAR-MUC1 T cells agglomerate around tumor cells; In CAR-MUC1-IL22 T cells group, large number of CAR-MUC1-IL22 T cells agglomerate around tumor cells (Red arrow is point to the tumor cell; the blue arrow is point to the T cell or two kinds of CAR-T cells).

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.10 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with tumor cell after for 72 h.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.10 In vitro antitumor efficacy of CAR-MUC1 T cells co-culture with tumor cell after for 72 h.

Three different T cells were incubated with tumor cell (Cal33) and non-neoplastic epithelial cell (OME) at a low E/T ratio (1:1; 1:2; 1:5; 1:10) for 72 h,
flow cytometry tested the apoptosis rate of tumor cells.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.11 Representative T-cell expansion profile of three different T cells.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.11 Representative T-cell expansion profile of three different T cells.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.12 ELISA detected the secretion of IL22 in the culture supernatant.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.12 ELISA detected the secretion of IL22 in the culture supernatant.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.13 ELISA detected the secretion of IL22 in the coculture supernatant of different E/T ratio.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.13 ELISA detected the secretion of IL22 in the coculture supernatant of different E/T ratio.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.14 ELISA detected the secretion of IL-2/IFN-γ/TNF-α in the coculture supernatant of low E/T ratio.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.14 ELISA detected the secretion of IL-2/IFN-γ/TNF-α in the coculture supernatant of low E/T ratio.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.15 CAR-T cells induce tumor degradation of HNSCC in vivo.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.15 CAR-T cells induce tumor degradation of HNSCC in vivo.

1E6 fLuc+ HN4 tumor cells were injected into the subcutaneous tissue in NSG mouse. After 10 d, tail intravenous injection of CAR T cells (n = 5). The mice were sacrificed on day 40 for tumor analysis. B, Bioluminescence images of four treatment groups mice.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.16 CAR-T cells induce tumor degradation of HNSCC in vivo.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.16 CAR-T cells induce tumor degradation of HNSCC in vivo.

Total body bioluminescence units quantitate were measured by bioluminescence photometry and flux values (photons per second, P < .001).

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.17 CAR-T cells induce tumor degradation of HNSCC in vivo.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.17 CAR-T cells induce tumor degradation of HNSCC in vivo.

Tumor volume growth curves of four treatment groups (P < .001).

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.18 CAR-T cells induce tumor degradation of HNSCC in vivo.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.18 CAR-T cells induce tumor degradation of HNSCC in vivo.

T-cell infiltration statistics in four treatment groups (P < .01).

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

Complete CAR data Funcs

Fig.19 CAR-T cells induce tumor degradation of HNSCC in vivo.

CAR Construction : SM3/HMFG2 scfv-41BB-CD3ζ-IL22 Latest CAR Construction

Fig.19 CAR-T cells induce tumor degradation of HNSCC in vivo.

CD3 in tumor tissue was detected using the anti-CD3 antibody (Abcam 5690, dilution 1:200); cell nuclei were stained with DAPI.

Mei, Z., Zhang, K., Lam, A. K. Y., Huang, J., Qiu, F., Qiao, B., & Zhang, Y. (2020). MUC1 as a target for CAR‐T therapy in head and neck squamous cell carinoma. Cancer medicine, 9(2), 640-652.

More Published Data More Published Data

Customer Reviews and Q&As

There are currently no customer reviews or questions for Anti-MUC1 scFv h(CD4-FcεRIγ) CART, pCDCAR1 (CAR-T-2-M303-4G). Click the button below to contact us or submit your feedback about this product.

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.

Related Products

Online Inquiry

For any technical issues or product/service related questions, please leave your information below. Our team will contact you soon.

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Key Updates
Newsletter NEWSLETTER

The latest newsletter to introduce the latest breaking information, our site updates, field and other scientific news, important events, and insights from industry leaders

LEARN MORE NEWSLETTER
New Solution NEW SOLUTION

CellRapeutics™ In Vivo Cell Engineering: One-stop in vivo T/B/NK cell and macrophage engineering services covering vectors construction to function verification.

LEARN MORE SOLUTION
NOVEL SOLUTION NOVEL TECHNOLOGY

Silence™ CAR-T Cell: A novel platform to enhance CAR-T cell immunotherapy by combining RNAi technology to suppress genes that may impede CAR functionality.

LEARN MORE NOVEL TECHNOLOGY
NEW TECHNOLOGY NEW SOLUTION

Canine CAR-T Therapy Development: From early target discovery, CAR design and construction, cell culture, and transfection, to in vitro and in vivo function validation.

LEARN MORE SOLUTION
Receive our latest news and insights.