Between Embryonic (E) day 21 and 22, rats received an injection of either lipopolysaccharide (LPS) (100μg/kg) or its saline vehicle at equal volume. Animals were euthanized on day of birth (P0) or at least 24 hours after the injection for non-pregnant animals. A. In the mPFC, analysis of CD11b expression revealed an interaction of pregnancy and immune activation. Post hoc analysis indicated the Postpartum, LPS-treated group had significantly lower expression than the Non-pregnant, LPS-treated group. B. IL-1β analysis revealed a significant interaction of pregnancy and immune activation. Post hoc analysis revealed trends that the Pregnant, LPS-treated group had lower expression than the Non-pregnant, LPS-treated and Postpartum, Saline-treated groups (p < 0.08). C. Analysis of IL-6 showed a significant main effect of pregnancy and an interaction of pregnancy and immune activation such that the Postpartum, Saline-treated animals and the Non-pregnant, LPS-treated animals had significantly higher expression compared to Non-pregnant, Saline-treated controls. D, E. IL-4 and BDNF analysis revealed a significant main effect of reproductive state in that only postpartum females showed higher gene expression relative to non-pregnant rats. F. In the HP, analysis of IL-1β showed a main effect of treatment. Only the Non-pregnant, LPS-treated group showed significantly higher gene expression compared to the other three groups (p < 0.05). G, H. IL-6 and IL-4 showed a main effect of pregnancy such that postpartum rats showed higher gene expression relative to the non-pregnant groups. No significant differences were found for CD11b or BDNF in the HP (not shown). *: p < 0.05; **: p < 0.001, #: p < 0.08