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Immuno-oncology has become a crucial pillar of therapy against cancer. Antibody-based biologics that target immune checkpoint inhibitors were the first-generation cancer immunotherapy developed and show remarkable efficacy in patients with advanced cancer. Unfortunately, not all patients benefit from these therapies due to various resistance mechanisms in tumours, leading to diminished efficacy and ultimately to tumour persistence or rebound. Despite these challenges, the field of immunotherapy continues to grow and its focus now includes various therapeutic approaches modulating one or more human immune cell types.
The tumour microenvironment is intricately complex, conditioning stromal cells to support cancer cell viability, proliferation, and resistance to anti-cancer immunotherapies. Understanding the molecular underpinnings of these processes is crucial for identifying promising targets for pharmacological inhibition. We offer in vitro assays that faithfully recapitulate cancer pathology, aiding in holistic research.
· M2-like macrophage differentiation assay
· M2-like reprogramming assay
· M2-like mediated T cell suppression assay
· M2-like mediated EMT assay
· M2-like phagocytosis and efferocytosis assay
· DC activation assay
· DC-Tcell coculture assay (MLR, autologous assay using peptide pools)
· MDSC-mediatedT cell suppression
· Tcell activation assays (PBMC and CD3+)
· DC-Tcell coculture assay (MLR, autologous assay using peptide pools)
· Tcell-mediated tumour cell killing assay
· ExhaustedT cell assay
· Tcell chemotaxis assay
· iTreg differentiation assay
· iTreg and nTreg suppression assay
· NKcell activation assay
· NKcell natural cytotoxicity assay
· Antibody mediated cellular cytotoxicity assay (ADCC)
· Cancer-associated fibroblast (CAF) activation assay
· Cancercell growth and apoptosis assay using 2D and 3D spheroid model
· Cancercell migration assay (EMT assay)
· Immunogeniccell death assay
Our team can help you accelerate your project to clinic: talk directly to an expert about your specific needs.