2022 April 12
AACR Conference (poster 3599)
Interleukin-10 and transforming growth factor-b do not suppress tumor killing activity of PBMC-derived SUPLEXA cells
- The manufacture of SUPLEXA cells from PBMCs generates immune effector cell types with potent and broad tumor cell killing activity.
- Comprehensive phenotyping of SUPLEXA cells by CyTOF indicates that SUPLEXA cells are a mixture of NK cells, CD8+ T cells, CD56+ NK-like T cells, TCRγδ cells, and CD4 T cells that express high-levels of killer cell factors (granzymes and perforin) and activation markers (not shown).
- IL-10 significantly enhanced the killing activity and production of IFNγ, MIP-1α, and Rantes by SUPLEXA cells in a dose-dependent fashion.
- TGFβ1 modestly suppressed SUPLEXA cell mediated tumor cell killing activity and reduced IFNγ and MIP-1α production.
- SUPLEXA cells are entering Phase 1 clinical testing in Australia.