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Induction of Maternal Immune Activation in Mice at Mid-gestation Stage with Viral Mimic Poly(I:C)
Published on: March 25, 2016
Effects of maternal autoantibody exposure at the cellular level: implications for the developing brain
Katelien H Blumenthal1, Janna McLellan1, Judy Van de Water1,2
1Division of Rheumatology, Allergy, and Clinical Immunology, Department of Internal Medicine, University of California, Davis, Davis, CA, United States.
Maternal autoantibodies (aABs) linked to autism can affect fetal brain development. This review explores how these autoantibodies may impact brain cells and lead to autism in children.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Maternal autoimmunity during pregnancy is linked to fetal development issues.
- Maternal autoantibody-related autism (MARA) involves autoantibodies targeting fetal brain proteins, associated with autism diagnoses.
- Specific autoantibody targets and maternal patterns are identified in MARA, differentiating mothers of children with autism from controls.
Purpose of the Study:
- To review potential mechanisms by which MARA autoantibodies interact with cells in the developing brain.
- To highlight the impact of these interactions on cellular development and their contribution to autism.
Main Methods:
- Review of clinical studies identifying MARA autoantibody targets and patterns.
- Analysis of rodent studies demonstrating gestational exposure effects of MARA autoantibodies on offspring brain development and behavior.
- Discussion of cellular-level interactions between autoantibodies, autoantigens, and neuronal/non-neuronal cells.
Main Results:
- Maternal autoantibodies targeting specific fetal brain proteins are associated with autism.
- Gestational exposure to these autoantibodies alters offspring brain development and behavior in animal models.
- Identified autoantibody patterns in mothers of children with autism differ from mothers of neurotypical children.
Conclusions:
- MARA autoantibodies may influence autism development by interacting with key cells and autoantigens in the developing brain.
- These interactions can alter cellular developmental trajectories, potentially leading to autism.
- Understanding these mechanisms is crucial for further research into MARA and autism.
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