

Allogenic CAR-T cell therapy without gene editing
Tuesday, November 3, 2020 1:00 PM to 1:25 PM · 25 min. (Africa/Abidjan)
World Immunotherapy Congress
Cellular immunotherapy
Presentation
Information
- Celyad utilizes two technologies based on non-gene edited approaches to modulate the T-cell receptor (TCR) complex to generate allogeneic CAR-T therapies.
- The first approach utilizes our TCR-inhibitor molecule (TIM) and is tailored to our NKG2D-based CAR-T clinical candidate CYAD-101
- The second approach leverages shRNA technology to knockdown the expression of the TCR on the surface of the T-cell and is used in CYAD-200 series
Laure Twyffels, Research & Development Manager, Celyad Oncology
