Back to Search
Start Over
Efficacy of anti-CD147 chimeric antigen receptors targeting hepatocellular carcinoma.
- Source :
-
Nature communications [Nat Commun] 2020 Sep 23; Vol. 11 (1), pp. 4810. Date of Electronic Publication: 2020 Sep 23. - Publication Year :
- 2020
-
Abstract
- Chimeric antigen receptor (CAR) therapy is a promising immunotherapeutic strategy for treating multiple refractory blood cancers, but further advances are required for solid tumor CAR therapy. One challenge is identifying a safe and effective tumor antigen. Here, we devise a strategy for targeting hepatocellular carcinoma (HCC, one of the deadliest malignancies). We report that T and NK cells transduced with a CAR that recognizes the surface marker, CD147, also known as Basigin, can effectively kill various malignant HCC cell lines in vitro, and HCC tumors in xenograft and patient-derived xenograft mouse models. To minimize any on-target/off-tumor toxicity, we use logic-gated (log) GPC3-synNotch-inducible CD147-CAR to target HCC. LogCD147-CAR selectively kills dual antigen (GPC3 <superscript>+</superscript> CD147 <superscript>+</superscript> ), but not single antigen (GPC3 <superscript>-</superscript> CD147 <superscript>+</superscript> ) positive HCC cells and does not cause severe on-target/off-tumor toxicity in a human CD147 transgenic mouse model. In conclusion, these findings support the therapeutic potential of CD147-CAR-modified immune cells for HCC patients.
- Subjects :
- Animals
Basigin genetics
Carcinoma, Hepatocellular pathology
Cell Line, Tumor
Disease Models, Animal
Female
Hep G2 Cells
Humans
Killer Cells, Natural
Liver pathology
Liver Neoplasms pathology
Male
Mice
Mice, Knockout
Mice, Transgenic
Xenograft Model Antitumor Assays
Basigin metabolism
Carcinoma, Hepatocellular drug therapy
Carcinoma, Hepatocellular metabolism
Immunotherapy, Adoptive methods
Liver Neoplasms drug therapy
Receptors, Chimeric Antigen drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 32968061
- Full Text :
- https://doi.org/10.1038/s41467-020-18444-2