On phagocytic cells, also called macrophages, and other immune cells the ligand for CD47, namely SIRPa, can be found. When SIRPα binds to CD47, this triggers a signal which prevents the killing of the target cell. Most tumor cells also produce high amounts of CD47 and hence prevent being attacked by immune cells. Current tumor therapies using antibodies could block CD47 and at the same time activate immune cells. Nevertheless, serious side effects to healthy organs and blood cells limit this approach.
The novel therapy concept presented here ensures that tumor cells on their own produce a CD47-blocking and immune activating protein. For this, scientists introduced a DNA gene vector into the tumor cells. DNA sequences were designed to ensure the expression of a protein with maximized CD47-blocking and immune activating properties. After successful DNA transfer, tumor cells produced and secreted the protein into the tumor vicinity.
Results: CD47 was successfully blocked not only on tumors cells producing the fusion protein but also on the tumor cells in their vicinity. Tumor growth was stopped and one third of tumors were eradicated, when applying this therapy in an in vivo model of highly malignant human breast cancer. "We observed a tumor infiltration of macrophages, which was due to the therapy. Also, other immune cells recognized and destroyed tumors cells marked with fusion protein. We were relieved, that we did not observe any organ related toxicities", Manfred Ogris explains. "Next we aim at a further optimization of this approach, which should enable further preclinical studies paving the way for a potential new tumor therapy."
Publication in Molecular Therapy Oncolytics:
CD47-targeted cancer immunogene therapy: secreted SIRPα-Fc fusion protein eradicates tumors by macrophage and NK cell activation: Manfred Ogris et al.
CD47-targeted cancer immunogene therapy: secreted SIRPα-Fc fusion protein eradicates tumors by macrophage and NK cell activation
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