Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5666730 | Immunology Letters | 2017 | 8 Pages |
â¢Myeloid-derived suppressor cells (MDSCs) are important mediators of the immune cells.â¢MDSCs impair B-cell proliferation and induce B-cell death.â¢MDSCs decrease B-cell IgM responses and down regulate the expression of important ctivation surface markers.â¢MDSCs use of reactive oxygen species (ROS), arginase-1, and nitric oxide (NO) to modulate B-cell immune responses.
Myeloid-derived suppressor cells (MDSCs) are key regulators of adaptive immunity by suppressing T-cell functions. However, their potential action on or interaction with B cells remained poorly understood. Here we demonstrate that human polymorphonuclear MDSCs differentially modulate B-cell function by suppressing B-cell proliferation and antibody production. We further demonstrate that this MDSC-mediated effect is cell contact dependent and involves established mediators such as arginase-1, nitric oxide (NO), reactive oxygen species (ROS) as well as B-cell death. Collectively, our studies provide novel evidence that human MDSCs modulate B cells, which could have future implications for immunotherapy approaches.