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Today, Immuno-Oncology focuses on ways to promote patient immune system ability to fight tumoral invasion through combinations of different treatments, including monoclonal antibodies, vaccines, immune checkpoints, CAR-T cells or small molecules.

All these rely on the 3 major components of the immune system: T cells, B cells and sentinel cells.

Whether you need to understand a treatment’s mechanism of action through pathway dissection or to set up a functional readout like cytokine release, we have specific assays ready for you.

T cell receptor

T cell activation or blockade is probably the main focus of immuno-oncology, whether in CAR-T cells (chimeric antigen receptor), checkpoint blockade inhibition, or T cell infiltration.

Understanding TCR (T cell receptor) signaling is essential to assess a potential treatment and its effects.


B cell receptor

As a heterogeneous population, B cells can be involved in several aspects of immunotherapy. They can produce pro- or anti-inflammatory cytokines, and B cell infiltration in the tumor micro-environment (TME) can be linked to a better prognosis.

Understanding B cell activation through the BCR (B cell receptor) is now a focus in immuno-oncology.


Toll like receptor

TLR are a large family of receptors expressed by sentinel cells, and play a pivotal role in innate immunity.

Ligands for TLR have been widely studied as anti-cancer therapies but the outcome is as yet unpredictable. TLR are therefore a new avenue to explore for potential cancer treatments.