Effects of IFNγ and IL4 rich microenvironment on porcine monocyte-derived dendritic cell activation in vitro

Dendritic cells (DCs) represent a heterogeneous group of major antigen-presenting cells, responding to different stimuli in their microenvironment. They are able to activate naive T-cells and drive their polarization towards effector types. However, the effect of different Th-polarizing cytokine microenvironment on porcine DCs remains poorly described. Therefore, the effect of IFN gamma or IL4 rich microenvimnment on porcine monocyte-derived dendritic cells and their activation, antigen recognition and cytokine secretion towards T-cell polarization were studied in vitro. IFN gamma-rich microenvimnment induced a higher proinflammatory response and release of Th1/Th17-polarizing cytokines (IL1 beta, IL12p35, IL23p19), while anti-inflammatory properties (IL10, TGF beta) was not affected by a cytokine micmenvironment. From the achieved results, we propose that different cytokine microenvimnment has the potential to modulate dendritic cells and their ability to activate T-cells.

Automated summary

This study investigated the effects of different cytokine microenvironments on porcine dendritic cells and found that an IFNγ-rich microenvironment induced a higher inflammatory response and release of polarizing cytokines. Different cytokine microenvironments have the potential to modulate the activation ability of dendritic cells.