Schwartzer Jared J, Careaga Milo, Coburn Morgan A, Rose Destanie R, Hughes Heather K, Ashwood Paul
Program in Neuroscience and Behavior, Department of Psychology and Education, Mount Holyoke College, 50 College Street, South Hadley, MA 01075, United States.
The M.I.N.D. Institute, University of California, Davis, 2825 50th Street, Sacramento, CA 95817, United States; Department of Medical Microbiology and Immunology, University of California, Davis, One Shields Avenue, Davis, CA 95616, United States.
Brain Behav Immun. 2017 Jul;63:99-107. doi: 10.1016/j.bbi.2016.09.007. Epub 2016 Sep 10.
Recent population-based studies of expecting mothers identified a unique profile of immune markers that are associated with an increased risk of having a child diagnosed with autism spectrum disorder (ASD). This immune profile, including increased levels of maternal and placental interleukin (IL)-4 and IL-5, is consistent with an immune response found in an allergic-asthma phenotype. Allergies and asthma reflect an imbalance in immune responses including polarization towards T-helper type 2 (T2) responses, with both genetic susceptibility and environmental factors affecting this T-cell polarization. Mouse strains provide a known and controlled source of genetic diversity to explore the role of genetic predisposition on environmental factors. In particular, the FVB background exhibits a skew towards T2-mediated allergic-asthma response in traditional models of asthma whereas the C57 strain exhibits a more blunted T2 polarized phenotype resulting in an attenuated allergic-asthma response. C57BL/6J (C57) and the sighted FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant (FVB/Ant) lines were selected based on their characteristic high sociability and differing sensitivity to T2-mediated stimuli. Based on the distinct allergy-sensitive immune responses of these two strains, we hypothesized that unique developmental consequences would occur in offspring following maternal allergy-asthma exposure. Female C57 and FVB/Ant dams were primed/sensitized with an exposure to ovalbumin (OVA) before pregnancy, then exposed to either aerosolized OVA or PBS-vehicle throughout gestation. Sera from pregnant dams were analyzed for changes in cytokine profiles using multiplex-arrays and offspring were assessed for changes in autism-like behavioral responses. Analysis of maternal sera revealed elevated IL-4 and IL-5 in OVA-treated dams of both strains but only C57 mice expressed increased levels of IL-1β, IL-6, TNFα, and IL-17. Behavioral assessments revealed strain-dependent changes in juvenile reciprocal social interaction in offspring of maternal allergic asthma dams. Moreover, mice of both strains showed decreased repetitive grooming and increased marble burying behavior when born to OVA-exposed dams. Together, these findings support the important role genetic predisposition plays in the effects of maternal immune activation and underscore differences in ASD-like behavioral outcomes across mouse strains.
最近基于人群的对孕妇的研究确定了一种独特的免疫标志物特征,这些标志物与孩子被诊断为自闭症谱系障碍(ASD)的风险增加有关。这种免疫特征,包括母体和胎盘白细胞介素(IL)-4和IL-5水平升高,与在过敏性哮喘表型中发现的免疫反应一致。过敏和哮喘反映了免疫反应的失衡,包括向辅助性T细胞2型(T2)反应的极化,遗传易感性和环境因素都会影响这种T细胞极化。小鼠品系提供了一个已知且可控的遗传多样性来源,以探索遗传易感性对环境因素的作用。特别是,在传统哮喘模型中,FVB背景表现出向T2介导的过敏性哮喘反应的偏向,而C57品系表现出更不明显的T2极化表型,导致过敏性哮喘反应减弱。C57BL/6J(C57)和有视力的FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant(FVB/Ant)品系是根据它们特有的高社交性和对T2介导刺激的不同敏感性选择的。基于这两个品系不同的过敏敏感免疫反应,我们假设母体过敏性哮喘暴露后,后代会出现独特的发育后果。雌性C57和FVB/Ant母鼠在怀孕前用卵清蛋白(OVA)进行激发/致敏,然后在整个妊娠期暴露于雾化OVA或PBS载体。使用多重阵列分析怀孕母鼠血清中细胞因子谱的变化,并评估后代自闭症样行为反应的变化。对母体血清的分析显示,两种品系经OVA处理的母鼠中IL-4和IL-5升高,但只有C57小鼠的IL-1β、IL-6、TNFα和IL-17水平升高。行为评估显示,母体过敏性哮喘母鼠后代的幼年相互社交互动存在品系依赖性变化。此外,当出生于暴露于OVA的母鼠时,两种品系的小鼠都表现出重复梳理行为减少和埋大理石行为增加。总之,这些发现支持了遗传易感性在母体免疫激活影响中所起的重要作用,并强调了不同小鼠品系在ASD样行为结果上的差异。