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New T-Cell Therapies for Brain Metastasis, CD133 in the Driver's Seat
Anthony R Sloan1,2, Mihika Thapliyal1,3, Justin D Lathia1,2,3,4
1Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Abstract:
Chimeric antigen receptor (CAR)-T cell immunotherapy has revolutionized cancer therapy for some advanced cancers, but success is predicated on identifying the correct cell surface target. In a recent article, the authors leveraged the cancer stem cell surface antigen CD133 to develop a CAR-T therapy for brain metastasis. See related article by Kieliszek et al., p. 554.
Insights
Researchers developed a new CAR-T cell therapy targeting the CD133 antigen on cancer stem cells. This approach aims to improve treatment for brain metastasis by targeting a key cancer cell surface marker.
Area of Science:
- Oncology
- Immunotherapy
- Cancer Stem Cell Biology
Background:
- Chimeric antigen receptor (CAR)-T cell therapy shows promise for advanced cancers.
- Effective CAR-T therapy relies on identifying specific cancer cell surface targets.
- Brain metastasis presents unique therapeutic challenges.
Purpose of the Study:
- To develop a novel CAR-T cell therapy for brain metastasis.
- To utilize the cancer stem cell surface antigen CD133 as a therapeutic target.
Main Methods:
- Leveraging the CD133 antigen for CAR-T cell therapy development.
- Application of CAR-T cell immunotherapy in the context of brain metastasis.
Main Results:
- Successful development of a CAR-T therapy targeting CD133.
- Potential for improved efficacy in treating brain metastasis.
Conclusions:
- Targeting CD133 with CAR-T cells is a viable strategy for brain metastasis.
- This approach offers a new avenue for advanced cancer treatment.
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