Cellular-mediated and humoral immunity in children with autism

IF 0.2 Q4 ALLERGY
S. A. El-Aziz, R. El-Din
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引用次数: 1

Abstract

Background: Autism spectrum disorder (ASD) is a spectrum of behavioral anomalies characterized by impaired social interaction and communication, often accompanied by repetitive and stereotyped behavior. The condition manifests within the first 3 years of life and persists into adulthood. There are numerous hypotheses regarding the etiology and pathology of ASD, including a suggested role for immune dysfunction. While immune system abnormalities have been reported in children with autistic disorder, there is little consensus regarding the nature of these differences which include both enhanced autoimmunity and reduced immune function. It has long been known that extensive interactions occur between the immune system and neuronal system/brain, and that normal neurodevelopment is contingent upon an appropriate interaction with the immune system. Objectives: the aim of the present study was to evaluate the cell mediated and humoral immunity of children with autism through evaluation of the serum antibody levels of immunoglobulin (IgG, IgM, IgA), also we evaluated the T helper and T suppressor cells (CD4 and CD8 T cell subpopulations) and CD4/CD8 ratio in children with autism and compared with the healthy control children. Methods: This study was carried out in the Psychiatry Unit, Department of Pediatrics, Tanta University Hospital. Thirty children with autism (24 males, 6 females) newly diagnosed were included in the study, their age range was (3-9 years) with the mean age of 51.8 years. Childhood Autism Rating Scale (CARS) was used for the diagnosis of autism. Diagnosis of autism was based also, on the criteria for the diagnosis of autism that are set out in the Diagnostic and Statistical Manual of Mental Disorders DSM-IVTR (Fourth Edition, Text Revision). The intial Childhood Autism Rating Scale (CARS) score for these children was ≥30, as children with a CARS score ≥30 were considered to have autism. Intial CARS score range for children with autism was (31-60). The control group consisted of thirty healthy children (10 females, 20 males). Their age range was (2-10 years) and the mean age was 5.3 ± 2.4 years. Results: Children with autism had significantly lower serum levels of IgG, IgA and IgM compared to the control children p < 0.001. Also children with autism had significantly lower numbers of CD4 cells with increased CD8+ T cell subpopulations and decreased CD4+/CD8+ ratio. Conclusion: Children with autism have significantly reduced levels of serum IgG, IgA and IgM compared to the control children, suggesting an underlying defect in the immune function, also the cell-mediated immunity is impaired as evidenced by low numbers of CD4+ cells and increased CD8+ T cell subpopulations and decreased CD4+/CD8+ ratio. Keywords: autism spectrum disorder (ASD), neurodevelopment, immunity Egypt J Pediatr Allergy Immunol 2012;10(1):25-32.
自闭症儿童的细胞介导和体液免疫
背景:自闭症谱系障碍(ASD)是一种以社会互动和沟通障碍为特征的行为异常,通常伴有重复和刻板的行为。这种情况出现在生命的头3年,并持续到成年。关于ASD的病因和病理有许多假设,包括免疫功能障碍的作用。虽然免疫系统异常在自闭症儿童中有报道,但对于这些差异的本质,包括增强的自身免疫和降低的免疫功能,几乎没有共识。人们早就知道免疫系统和神经系统/大脑之间存在广泛的相互作用,正常的神经发育取决于与免疫系统的适当相互作用。目的:本研究旨在通过评价自闭症儿童血清免疫球蛋白(IgG、IgM、IgA)抗体水平,评价自闭症儿童的T辅助细胞和T抑制细胞(CD4和CD8 T细胞亚群)和CD4/CD8比值,并与健康对照进行比较,评价自闭症儿童的细胞介导免疫和体液免疫。方法:本研究在坦塔大学附属医院儿科精神科进行。新诊断的自闭症患儿30例(男24例,女6例),年龄3 ~ 9岁,平均年龄5岁1.8岁。儿童自闭症评定量表(CARS)用于自闭症的诊断。自闭症的诊断也是基于精神疾病诊断与统计手册DSM-IVTR(第四版,文本修订)中列出的自闭症诊断标准。这些儿童的初始儿童自闭症评定量表(CARS)得分≥30分,因为CARS得分≥30分的儿童被认为患有自闭症。自闭症儿童的初始CARS评分范围为(31-60)。对照组为30例健康儿童(女10例,男20例)。年龄2 ~ 10岁,平均5.3±2.4岁。结果:自闭症患儿血清IgG、IgA、IgM水平显著低于对照组(p < 0.001)。此外,自闭症儿童的CD4细胞数量明显减少,CD8+ T细胞亚群增加,CD4+/CD8+比值降低。结论:自闭症儿童血清IgG、IgA和IgM水平明显低于正常儿童,提示其免疫功能存在潜在缺陷,CD4+细胞数量减少,CD8+ T细胞亚群增加,CD4+/CD8+比值降低,细胞免疫功能受损。关键词:自闭症谱系障碍(ASD),神经发育,免疫埃及[J] .儿科变态反应与免疫,2012;10(1):25-32。
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