Autism-specific maternal autoantibodies recognize critical proteins in developing brain

被引:189
作者
Braunschweig, D. [1 ,2 ,3 ]
Krakowiak, P. [4 ]
Duncanson, P. [1 ,2 ,3 ]
Boyce, R. [1 ,2 ,3 ]
Hansen, R. L. [2 ,3 ,5 ]
Ashwood, P. [2 ,3 ,6 ]
Hertz-Picciotto, I. [2 ,3 ,4 ]
Pessah, I. N. [2 ,3 ,7 ]
Van de Water, J. [1 ,2 ,3 ]
机构
[1] Univ Calif Davis, Dept Internal Med, Davis, CA 95616 USA
[2] Univ Calif, Davis MIND Inst, Davis, CA USA
[3] Univ Calif Davis, Childrens Ctr Environm Hlth, Davis, CA 95616 USA
[4] Univ Calif Davis, Dept Publ Hlth Sci, Div Epidemiol, Davis, CA 95616 USA
[5] Univ Calif Davis, Dept Pediat, Davis, CA 95616 USA
[6] Univ Calif Davis, Dept Med Microbiol, Davis, CA 95616 USA
[7] Univ Calif Davis, Sch Vet Med, Dept Mol Biosci, Davis, CA 95616 USA
关键词
autism; autoantibodies; fetal brain; neurodevelopment; STRESS-INDUCIBLE PROTEIN-1; RESPONSE MEDIATOR PROTEINS; FETAL-BRAIN; SPECTRUM DISORDERS; IMMUNOGLOBULIN-G; IGG ANTIBODIES; PRION PROTEIN; CHILDREN; EXPRESSION; NEURONS;
D O I
10.1038/tp.2013.50
中图分类号
R749 [精神病学];
学科分类号
100204 [神经病学];
摘要
Autism spectrum disorders (ASDs) are neurodevelopmental in origin, affecting an estimated 1 in 88 children in the United States. We previously described ASD-specific maternal autoantibodies that recognize fetal brain antigens. Herein, we demonstrate that lactate dehydrogenase A and B (LDH), cypin, stress-induced phosphoprotein 1 (STIP1), collapsin response mediator proteins 1 and 2 (CRMP1, CRMP2) and Y-box-binding protein to comprise the seven primary antigens of maternal autoantibody-related (MAR) autism. Exclusive reactivity to specific antigen combinations was noted in 23% of mothers of ASD children and only 1% of controls. ASD children from mothers with specific reactivity to LDH, STIP1 and CRMP1 and/or cypin (7% vs 0% in controls; P < 0.0002; odds ratios of 24.2 (95% confidence interval: 1.45-405)) had elevated stereotypical behaviors compared with ASD children from mothers lacking these antibodies. We describe the first panel of clinically significant biomarkers with over 99% specificity for autism risk thereby advancing our understanding of the etiologic mechanisms and therapeutic possibilities for MAR autism.
引用
收藏
页码:e277 / e277
页数:9
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