Technology ID
TAB-4196

Combination of recombinant IL-7 with Chimeric Antigen Receptor (CAR) T Cells Targeting Glypican-3 (GPC3) for the Treatment of Hepatocellular Carcinoma (HCC)

E-Numbers
E-108-2021-0
Lead Inventor
Ho, Mitchell (NCI)
Co-Inventors
Li, Dan (NCI)
Lee, Byung Ha (NeoImmuneTech, Inc)
Ferrando-Martinez, Sara (NeoImmuneTech, Inc)
Applications
Therapeutics
Therapeutic Areas
Oncology
Immunology
Development Stages
Pre-clinical (in vivo)
Lead IC
NCI
ICs
NCI

Hepatocellular carcinoma (HCC) is the most common type of liver cancer. standard treatment for HCC is not suitable for a large proportion of liver cancer patients. As a result, alternative treatments are needed. Chimeric antigen receptor (CAR) T cell therapy is a promising alternative approach selectively targets targeting tumors via tumor-specific antigens. However, to date, no effective CAR T cell therapy exists for HCC. 

Glypican-3 (GPC3) is a cell surface proteoglycan preferentially expressed in HCC. National Cancer Institute (NCI) researchers previously demonstrated that GPC3-targeting CAR T cell therapy was a promising therapeutic in preclinical animal models of HCC. Furthermore, it was reported that IL7 improved T cell or CAR T cell efficacy via enhancing CAR T cell persistence and survival. 

Researchers in the NCI’s Laboratory of Molecular Biology (LMB) found that a single treatment of a recombinant IL-7 significantly improved the efficacy of GPC3-targeted CAR T cell therapy for over 4 weeks in mice bearing human HCC tumors. The superior efficacy indicated that combination of recombinant IL-7 treatments with GPC3-targeting CAR T cells may improve the efficacy of treating HCC in patients.

Competitive Advantages:

Combining recombinant IL-7 with the CAR T cell therapy improves efficacy to treat HCC

 

Commercial Applications:

  • Combination immunotherapy for HCC

 

Licensing Contact: