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Targeting HLA-DR loss in hematologic malignancies with an inhibitory chimeric antigen receptor
- Source :
- Mol Ther
- Publication Year :
- 2021
- Publisher :
- American Society of Gene & Cell Therapy, 2021.
-
Abstract
- Chimeric antigen receptor natural killer (CAR-NK) cells have remarkable cytotoxicity against hematologic malignancies; however, they may also attack normal cells sharing the target antigen. Since human leukocyte antigen DR (HLA-DR) is reportedly lost or downregulated in a substantial proportion of hematologic malignancies, presumably a mechanism to escape immune surveillance, we hypothesize that the anti-cancer specificity of CAR-NK cells can be enhanced by activating them against cancer antigens while inhibiting them against HLA-DR. Here, we report the development of an anti-HLA-DR inhibitory CAR (iCAR) that can effectively suppress NK cell activation against HLA-DR-expressing cells. We show that dual CAR-NK cells, which co-express the anti-CD19 or CD33 activating CAR and the anti-HLA-DR iCAR, can preferentially target HLA-DR-negative cells over HLA-DR-positive cells in vitro. We additionally find that the HLA-DR-mediated inhibition is positively correlated with both iCAR and HLA-DR densities. We also find that HLA-DR-expressing surrounding cells do not affect the target selectivity of dual CAR-NK cells. Finally, we confirm that HLA-DR-positive cells are resistant to dual CAR-NK cell-mediated killing in a xenograft mouse model. Our approach holds great promise for enhancing CAR-NK and CAR-T cell specificity against malignancies with HLA-DR loss.
- Subjects :
- CD33
Cell
Biology
Immunotherapy, Adoptive
Mice
Antigen
Cell Line, Tumor
Neoplasms
Drug Discovery
Genetics
medicine
HLA-DR
Animals
Humans
Cytotoxicity
Molecular Biology
Pharmacology
Receptors, Chimeric Antigen
Cancer
HLA-DR Antigens
medicine.disease
Chimeric antigen receptor
In vitro
medicine.anatomical_structure
Hematologic Neoplasms
Cancer research
Molecular Medicine
Original Article
Iron-Dextran Complex
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Mol Ther
- Accession number :
- edsair.doi.dedup.....a75274fd3c1a562f942e309e3ca50383