Abbreviated Journal Title
CERIUM OXIDE NANOPARTICLES; DENDRITIC CELL MATURATION; ANTIGEN-PRESENTING CELLS; BLOOD MONONUCLEAR-CELLS; TH1 IMMUNE-RESPONSES; TITANIUM-DIOXIDE; REACTIVE OXYGEN; IN-VITRO; IMMUNOLOGICAL MODEL; CYTOKINE RELEASE; Multidisciplinary Sciences
Immunomodulation by nanoparticles, especially as related to the biochemical properties of these unique materials, has scarcely been explored. In an in vitro model of human immunity, we demonstrate two catalytic nanoparticles, TiO2 (oxidant) and CeO2 (antioxidant), have nearly opposite effects on human dendritic cells and T helper (T-H) cells. For example, whereas TiO2 nanoparticles potentiated DC maturation that led towards T(H)1-biased responses, treatment with antioxidant CeO2 nanoparticles induced APCs to secrete the anti-inflammatory cytokine, IL-10, and induce a T(H)2-dominated T cell profile. In subsequent studies, we demonstrate these results are likely explained by the disparate capacities of the nanoparticles to modulate ROS, since TiO2, but not CeO2 NPs, induced inflammatory responses through an ROS/inflammasome/IL-1 beta pathway. This novel capacity of metallic NPs to regulate innate and adaptive immunity in profoundly different directions via their ability to modulate dendritic cell function has strong implications for human health since unintentional exposure to these materials is common in modern societies.
Schanen, Brian C.; Das, Soumen; Reilly, Christopher M.; Warren, William L.; Self, William T.; Seal, Sudipta; and Drake, Donald R. III, "Immunomodulation and T Helper TH1/TH2 Response Polarization by CeO2 and TiO2 Nanoparticles" (2013). Faculty Bibliography 2010s. 4655.