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Serum autoantibodies to brain in Landau-Kleffner variant, autism, and other neurologic disorders
Oleh:
Connolly, Anne M.
;
Chez, Michael G.
;
Pestronk, Alan
;
Arnold, Susan T.
;
Mehta, Shobhna
;
Deuel, Ruthmary K.
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
The Journal of Pediatrics vol. 135 no. 05 (Nov. 1999)
,
page 607-613.
Topik:
ANA
;
Antinuclear antibody
;
ASD
;
Autistic spectrum disorder
;
EEG
;
Electroencephalogram
;
HC
;
Healthy children
;
LKS
;
Landau-Kleffner syndrome
;
LKSV
;
Landau-Kleffner syndrome variant
;
NNI
;
Non-neurologic illness
;
ONDs
;
Other neurologic disorders
;
PBS
;
Phosphate-buffered saline
Ketersediaan
Perpustakaan FK
Nomor Panggil:
J45.K.1999.02
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Objective: Etiologically unexplained disorders of language and social development have often been reported to improve in patients treated with immune-modulating regimens. Here we determined the frequency of autoantibodies to brain among such children. Design: We collected sera from a cohort of children with (1) pure Landau-Kleffner syndrome (n = 2), (2) Landau-Kleffner syndrome variant (LKSV, n = 11), and (3) autistic spectrum disorder (ASD, n = 11). None had received immune-modulating treatment before the serum sample was obtained. Control sera (n = 71) were from 29 healthy children, 22 with non-neurologic illnesses (NNIs), and 20 children with other neurologic disorders (ONDs). We identified brain autoantibodies by immunostaining of human temporal cortex and antinuclear autoantibodies using commercially available kits. Results: IgG anti-brain autoantibodies were present in 45% of sera from children with LKSV, 27% with ASD, and 10% with ONDs compared with 2% from healthy children and control children with NNIs. IgM autoantibodies were present in 36% of sera from children with ASD, 9% with LKSV, and 15% with ONDs compared with 0% of control sera. Labeling studies identified one antigenic target to be endothelial cells. Antinuclear antibodies with titers =1:80 were more common in children with ASD and control children with ONDs. Conclusion: Children with LKSV and ASD have a greater frequency of serum antibodies to brain endothelial cells and to nuclei than children with NNIs or healthy children. The presence of these antibodies raises the possibility that autoimmunity plays a role in the pathogenesis of language and social developmental abnormalities in a subset of children with these disorders.
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