The link between some alleles on human leukocyte antigen system and autism in children

被引:37
作者
Mostafa, Gehan A. [1 ,3 ]
Shehab, Abeer A. [2 ]
Al-Ayadhi, Laila Y. [3 ]
机构
[1] Ain Shams Univ, Dept Pediat, Fac Med, Cairo, Egypt
[2] Ain Shams Univ, Dept Clin Pathol, Fac Med, Cairo, Egypt
[3] King Saud Univ, Autism Res & Treatment Ctr, Al Amodi Autism Res Chair, Dept Physiol,Fac Med, Riyadh, Saudi Arabia
关键词
Autism; Autoimmunity; Human leukocyte antigen system; Major histocompatibility complex; ELEVATED SERUM-LEVELS; INCREASED FREQUENCY; FAMILY-HISTORY; BASIC-PROTEIN; AUTOANTIBODIES; ASSOCIATION; ANTIBODIES; HLA; AUTOIMMUNITY; HLA-DR4;
D O I
10.1016/j.jneuroim.2012.10.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The reason behind the initiation of autoimmunity to brain in some patients with autism is not well understood. There is an association between some autoimmune disorders and specific alleles of human leukocyte antigen (HLA) system. Thus, we examined the frequency of some HLA-DRB1 alleles in 100 autistic children and 100 healthy matched-children by differential hybridization with sequence-specific oligonucleotide probes. The risk of association between acquisition or absence of these alleles and autism and also a history of autoimmune diseases in autistic relatives was studied. Autistic children had significantly higher frequency of HLA-DRB1*11 allele than controls (P<0.001). In contrast, autistic children had significantly lower frequency of HIA-DRB1*03 allele than controls (P<0.001). Acquisition of HLA-DRB1*011 and absence of HLA-DRB1*3 had significant risk for association with autism (odds ratio: 3.21 and 0.17, respectively; 95% CI: 1.65-631 and 0.06-0.45, respectively). HLA-DRB1*11 had a significant risk for association with a family history of autoimmunity in autistic children (odds ratio: 5.67; 95% CI: 2.07-16.3). In conclusions, the link of some HLA alleles to autism and to family history of autoimmunity indicates the possible contributing role of these alleles to autoimmunity in some autistic children. Despite a relatively small sample size, we are the first to report a probable protective association of HLA-DRB1*03 allele with autism. It warrants a replication study of a larger sample to validate the HLA-DRB1 genetic association with autism. This is important to determine whether therapeutic modulations of the immune function are legitimate avenues for novel therapy in selected cases of autism. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:70 / 74
页数:5
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