Maternal antibrain antibodies in autism

• Published in: Brain, behavior, and immunity Vol. 21; no. 3; pp. 351 - 357
• Main Authors: Zimmerman, Andrew W, Connors, Susan L, Matteson, Karla J, Lee, Li-Ching, Singer, Harvey S, Castaneda, Julian A, Pearce, David A
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01-03-2007
• Subjects: Adolescent; Adult; Allergy and Immunology; Animals; Antibodies; Antibody Formation; Autism; Autistic Disorder - immunology; Autoantibodies; Autoimmunity; Brain - immunology; Case-Control Studies; Child; Child, Preschool; Female; Humans; Male; Maternal; Maternal-Fetal Exchange; Middle Aged; Nerve Tissue Proteins - immunology; Pregnancy; Prenatal; Psychiatry; Autoimmunity; Prenatal; Antibodies; Autism; Maternal
• ISSN: 0889-1591; 1090-2139
• DOI: 10.1016/j.bbi.2006.08.005

Abstract Autism is a neurodevelopmental disorder of prenatal onset that is behaviorally defined. There is increasing evidence for systemic and neuroimmune mechanisms in children with autism. Although genetic factors are important, atypical prenatal maternal immune responses may also be linked to the pathogenesis of autism. We tested serum reactivity in 11 mothers and their autistic children, maternal controls, and several groups of control children, to prenatal, postnatal, and adult rat brain proteins, by immunoblotting. Similar patterns of reactivity to prenatal (gestational day 18), but not postnatal (day 8) or adult rat brain proteins were identified in autistic children, their mothers, and children with other neurodevelopmental disorders, and differed from mothers of normal children, normal siblings of children with autism and normal child controls. Specific patterns of antibody reactivity were present in sera from the autism mothers, from 2 to 18 years after the birth of their affected children and were unrelated to birth order. Immunoblotting using specific antigens for myelin basic protein (MBP) and glial acidic fibrillary protein (GFAP) suggests that these proteins were not targets of the maternal antibodies. The identification of specific serum antibodies in mothers of children with autism that recognize prenatally expressed brain antigens suggests that these autoantibodies could cross the placenta and alter fetal brain development.