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BY
THOMAS H. MAUGH II
Abnormal antibodies in maternal blood that bind
to fetal brain cells may contribute to the development
of autism, according to two new studies from the
MIND Institute at the University of California,
Davis.
Immunologist Judy Van de Water and her colleagues
isolated a form of antibody called "immunoglobulin
G," or IgG, from 61 mothers of autistic children
and found that in seven cases, it bound to two
proteins in fetal brain tissue.
Six of those mothers had children with regressive
autism, in which children appear to develop normally
for the first year or two before developing symptoms
such as loss of social or language skills.
The team also extracted IgG from 62 mothers whose
children were healthy. None of those antibodies
was able to bind to the fetal tissue proteins.
The studies' results will be published in the
March issue of the journal NeuroToxicology.
Following up on those findings, behavioral scientist
David Amaral of UC Davis and colleagues from the
California National Primate Research Center injected
four rhesus monkeys with human IgG from mothers
of autistic children three times near the end
of the first trimester of the monkeys' pregnancies.
All the offspring of the exposed monkeys demonstrated
repetitive behaviors that are analogous to those
exhibited by autistic children, such as pacing,
back-flipping, twirling and swinging more often
and for longer periods of times. The behaviors,
called "stereotypies," became more pronounced
after weaning and were more striking when the
animals were placed in unfamiliar settings.
Offspring of four female monkeys exposed to IgG
from mothers of healthy children showed no such
behaviors.
The study "links exposure to abnormal immune
system factors during pregnancy with specific
behavioral outcomes in offspring," Amaral
said.
The study was published online by the journal
Brain, Behavior and Immunity.
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