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1Translational Research Program, Abramson Cancer Center; Departments of Medicine and.
Abstract:
Chimeric antigen receptors redirect T cells to surface antigens. Discovery and validation of appropriate target antigens expands the possible indications for chimeric-antigen receptor (CAR) T cells. CS1 is expressed at high levels by multiple myeloma cells, but also to some extent on other lymphocytes. CS1 may be a viable target for CAR T cells in multiple myeloma.
Insights
Chimeric antigen receptor (CAR) T cells offer new cancer therapies. Researchers explored CS1 as a target for CAR T cells in multiple myeloma, finding it highly expressed on cancer cells but also on some healthy cells.
Area of Science:
- Immunology
- Oncology
- Cell Therapy
Background:
- Chimeric antigen receptors (CARs) are engineered receptors that redirect T cells to target specific surface antigens on cells.
- Expanding the range of targetable antigens is crucial for broadening the applications of CAR T-cell therapy.
- Multiple myeloma is a hematologic malignancy characterized by uncontrolled proliferation of plasma cells.
Purpose of the Study:
- To investigate the potential of CS1 as a target antigen for CAR T-cell therapy in multiple myeloma.
- To evaluate the expression profile of CS1 on multiple myeloma cells and other cell types.
Main Methods:
- Analysis of CS1 expression levels on multiple myeloma cells and normal lymphocytes.
- Assessment of CS1 as a potential target for CAR T-cell mediated cytotoxicity.
Main Results:
- CS1 is highly expressed on the surface of multiple myeloma cells.
- CS1 expression is also detected on other lymphocyte populations, indicating potential off-target effects.
- CS1 presents a viable, though not exclusive, target for CAR T-cell therapy in multiple myeloma.
Conclusions:
- CS1 is a promising target antigen for CAR T-cell therapy in multiple myeloma due to its high expression on cancer cells.
- Further research is needed to mitigate potential on-target, off-tumor toxicities associated with CS1 targeting on normal lymphocytes.
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