Abstract
T-cells genetically redirected with a chimeric antigen receptor (CAR) to recognize tumor antigens and kill tumor cells have been infused in several phase 1 clinical trials with success. Due to safety concerns related to on-target/off-tumor effects or cytokine release syndrome, however, strategies to prevent or abate serious adverse events are required. Pharmacologic therapies; suicide genes; or novel strategies to limit the cytotoxic effect only to malignant cells are under active investigations. In this review, we summarize results and toxicities of investigations employing CAR redirected T-cells, with a focus on published strategies to grant safety of this promising cellular application.
Original language | English (US) |
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Pages (from-to) | 230-249 |
Number of pages | 20 |
Journal | Pharmaceuticals |
Volume | 8 |
Issue number | 2 |
DOIs | |
State | Published - May 8 2015 |
All Science Journal Classification (ASJC) codes
- Molecular Medicine
- Pharmaceutical Science