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Flu & schizophrenia

Maternal immune activation influences fetal brain development through IL-6, linking infection to behavioral deficits in offspring.

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Maternal Immune Activation Alters Fetal Brain Development through Interleukin-6:

Schizophrenia and autism are thought to result from the interaction between a susceptibility genotype and environmental risk factors.

The offspring of women who experience infection while pregnant have an increased risk for these disorders. Maternal immune activation (MIA) in pregnant rodents produces offspring with abnormalities in behavior, histology, and gene expression that are reminiscent of schizophrenia and autism, making MIA a useful model of the disorders. However, the mechanism by which MIA causes long-term behavioral deficits in the offspring is unknown. Here we show that the cytokine interleukin-6 (IL-6) is critical for mediating the behavioral and transcriptional changes in the offspring. A single maternal injection of IL-6 on day 12.5 of mouse pregnancy causes prepulse inhibition (PPI) and latent inhibition (LI) deficits in the adult offspring. Moreover, coadministration of an anti-IL-6 antibody in the poly(I:C) model of MIA prevents the PPI, ...

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