Macrophage suppression assay
The tumor microenvironment (TME) can drive differentiation and accumulation of immune cells, which support tumor growth e.g. tumor-associated macrophages (TAMs) and M2 macrophages. We have a range of customizable assays to screen compounds for their potential to block these mechanisms, reducing the suppression of T cells and boosting anti-tumor responses. Reversal of T cell suppression can be measured by cytokine release (ELISA, multiplex or MSD), gene expression changes (qPCR) or by proliferation and activation markers using flow cytometry.
We are developing ex vivo protocols, utilizing tumor conditioned media (tumor cell lines and ascites samples) as well isolating TAMs, for use in our macrophage suppression assays as a translational step-up in complexity from our customizable in vitro assay systems.
MDSC suppression assay
Myeloid-derived suppressor cells (MDSC) are key players in the TME. Our MDSC-mediated T cell suppression assay can help you determine if your compound or biologic can block MDSC function and relieve T cell activation.
Treg supression assays
Regulatory T cells (Tregs) can inhibit unwanted immunity e.g. in autoimmune diseases, or conversely, they can suppress desirable immunity in cancer. We have a customizable Treg suppression assay to study your drug candidate’s ability to either boost or reduce Treg activity. We work closely with you to tailor key assay readouts to your requirements.
Our Treg suppression assays can incorporate in vitro generated inducible FoxP3+ Tregs (iTregs) or natural Tregs (nTregs) can be isolated for use in this assay, more closely reflecting the FoxP3-induction potentially driven by some tumor types and highly relevant to immuno-oncology research.
Please get in touch to discuss your T cell suppression assay study requirements.