
The study explores how the oncolytic measles virus (MV) interacts with macrophages and cancer cells in malignant pleural mesothelioma (MPM). MPM cells were found to drive monocytes to become M2-like macrophages, inhibiting viral protein expression in certain tumor cells. MV infection causes macrophages to produce antiviral and pro-inflammatory genes, enhancing immune response. These interactions create a pro-inflammatory tumor microenvironment, potentially boosting anti-tumor immunity.
Like
Save
Share