IL-38 inhibits microglial inflammatory mediators and is decreased in amygdala of children with autism spectrum disorder
Significance These findings indicate the important role of IL-38 in the inihibition of neurotensin-stimulated activation of microglia and the resulting release of proinflammatory molecules. Moreover, the reduced expression of IL-38 in the amygdala indicates that it may not be sufficient to prevent inflammation, and that its administration could serve as a novel treatment for children with autism spectrum disorder.
