Abstract
Autism spectrum disorder (ASD) is a neurodevelopmental disorder whose behavioral symptoms become apparent in early childhood. The underlying pathophysiological mechanisms are only partially understood and the clinical manifestations are heterogeneous in nature, which poses a major challenge for diagnosis, prognosis and intervention. In the last years, an important role of a dysregulated immune system in ASD has emerged, but the mechanisms connecting this to a disruption of brain development are still largely unknown. Although ASD is not considered as a typical autoimmune disease, self-reactive antibodies or autoantibodies against a wide variety of targets have been found in a subset of ASD patients. In addition, autoantibodies reactive to fetal brain proteins have also been described in the prenatal stage of neurodevelopment, where they can be transferred from the mother to the fetus by transplacental transport. In this review, we give an extensive overview of the antibodies described in ASD according to their target antigens, their different origins, and timing of exposure during neurodevelopment.
Highlights
Autism spectrum disorder (ASD) is a complex and highly heterogeneous neurodevelopmental disorder characterized by persistent deficits in social communication and social interaction [1]
We explore the current evidence of antibodies detected in ASD patients and in mothers of ASD patients, their possible role as biomarkers to support the disease diagnosis and their contribution in the understanding of disease mechanisms
Using a bigger cohort of 100 mothers of children with autistic disorder and 100 controls, immunoreactivity using Western blot against a 36 kDa human fetal brain protein was found in 10% of the mothers of ASD children (MASD) and only in 2% of the mothers with typically developing children (MTD) [128]
Summary
Autism spectrum disorder (ASD) is a complex and highly heterogeneous neurodevelopmental disorder characterized by persistent deficits in social communication and social interaction [1]. CAge range of study population; NA, not applicable; NR, not reported; MR, mental retardation; TD, typically developing; A, adults; DS, Down syndrome; OND, other neurological disorders; NNI, non-neurological illnesses; HC, healthy children; ADHD, attention-deficit/hyperactivity disorder; LKSV, Landau-Kleffner syndrome variant; AD, autoimmune disorder; DSM-III, Diagnostic and statistical manual of mental disorders third edition; DSM-IV, Diagnostic and statistical manual of mental disorders fourth edition; ADOS, Autistic Diagnostic Observation Schedule; ADI-R, Autism Diagnostic Interview-Revised; CARS, Chilhood autism rating scale; ABC, Autism behavior checklist.
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