4.6 Article

Cutting Edge: Critical Roles for Microbiota-Mediated Regulation of the Immune System in a Prenatal Immune Activation Model of Autism

Journal

JOURNAL OF IMMUNOLOGY
Volume 201, Issue 3, Pages 845-850

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1701755

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Funding

  1. Hartwell Foundation (Individual Biomedical Research Award)
  2. Owens Family Foundation
  3. Simons Foundation Autism Research Initiative [515305]
  4. National Institutes of Health/National Institute of General Medical Sciences predoctoral training grant [3T32GM008328]
  5. Medical Scientist Training Program at the University of Virginia [5T32GM007267-38]
  6. Hutcheson and Stull Undergraduate Research Fellowships

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Recent studies suggest that autism is often associated with dysregulated immune responses and altered micro biota composition. This has led to growing speculation about potential roles for hyperactive immune responses and the microbiome in autism. Yet how microbiome immune cross-talk contributes to neurodevelopmental disorders currently remains poorly understood. In this study, we report critical roles for prenatal micro biota composition in the development of behavioral abnormalities in a murine maternal immune activation (MIA) model of autism that is driven by the viral mimetic polyinosinic-polycytidylic acid. We show that preconception microbiota transplantation can transfer susceptibility to MIA-associated neurodevelopmental disease and that this is associated with modulation of the maternal immune response. Furthermore, we find that ablation of IL-17a signaling provides protection against the development of neurodevelopmental abnormalities in MIA offspring. Our findings suggest that microbiota landscape can influence MIA-induced neurodevelopmental disease pathogenesis and that this occurs as a result of microflora-associated calibration of gestational IL-17a responses.

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