Breast cancer-on-chip for patient-specific efficacy and safety testing of CAR-T cells
DOI:
10.1016/j.stem.2024.04.018
Publication Date:
2024-05-15T14:48:25Z
AUTHORS (12)
ABSTRACT
Physiologically relevant human models that recapitulate the challenges of solid tumors and tumor microenvironment (TME) are highly desired in chimeric antigen receptor (CAR)-T cell field. We developed a breast cancer-on-chip model with an integrated endothelial barrier enables transmigration perfused immune cells, their infiltration into tumor, concomitant monitoring cytokine release during culture over period up to 8 days. Here, we exemplified its use for investigating CAR-T efficacy ability control reaction pharmacological on/off switch. Additionally, primary cancer organoids study patient-specific efficacy. The modular architecture our tumor-on-chip paves way studying role other types TME thus provides potential broad application bench-to-bedside translation as well acceleration preclinical development products.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (66)
CITATIONS (18)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....