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Updated: Jan 21, 2026

Studying Interactions between Myeloid Cells and CAR T Cells In Vitro and In Vivo
Published on: July 25, 2025
Abstract:
Researchers have shown, preclinically, that the small-molecule inhibitor dasatinib can temporarily halt the action of chimeric antigen receptor (CAR) T cells without compromising therapeutic efficacy. Dasatinib's effects are reversible upon drug removal, and the hope is that this strategy could be used to mitigate cytokine release syndrome, a serious side effect of CAR T-cell therapy.
Insights
The small-molecule inhibitor dasatinib can temporarily pause chimeric antigen receptor (CAR) T-cell activity. This effect is reversible, offering a potential strategy to manage severe side effects like cytokine release syndrome in CAR T-cell therapy.
Area of Science:
- Immunology
- Pharmacology
- Oncology
Background:
- Chimeric antigen receptor (CAR) T-cell therapy is a promising cancer treatment.
- CAR T-cells can cause severe side effects, including cytokine release syndrome (CRS).
- Controlling CAR T-cell activity is crucial for managing toxicity.
Discussion:
- Preclinical studies demonstrate dasatinib's ability to temporarily inhibit CAR T-cell function.
- The inhibitory effect of dasatinib is reversible upon drug discontinuation.
- This reversibility is key to its potential therapeutic application.
Key Insights:
- Dasatinib acts as a reversible inhibitor for CAR T-cells.
- CAR T-cell efficacy is maintained despite temporary inhibition by dasatinib.
- This approach offers a novel method for controlling CAR T-cell activity.
Outlook:
- Dasatinib may provide a strategy to mitigate CRS and other toxicities associated with CAR T-cell therapy.
- Further clinical research is warranted to validate dasatinib's safety and efficacy in managing CAR T-cell therapy side effects.
- This reversible inhibition technique could enhance the therapeutic window of CAR T-cell treatments.
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