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自闭症谱系障碍患者血浆中的脑特异性自身抗体。

Brain-specific autoantibodies in the plasma of subjects with autistic spectrum disorder.

作者信息

Cabanlit Maricel, Wills Sharifia, Goines Paula, Ashwood Paul, Van de Water Judy

机构信息

Division of Rheumatology, Allergy and Clinical Immunology, UC Davis, Davis, CA 95616, USA.

出版信息

Ann N Y Acad Sci. 2007 Jun;1107:92-103. doi: 10.1196/annals.1381.010.

Abstract

Although autism spectrum disorder (ASD) is diagnosed on the basis of behavioral parameters, several studies have reported immune system abnormalities and suggest the possible role of autoimmunity in the pathogenesis of ASD. In this study we sought to assess the incidence of brain-specific autoantibodies in the plasma of children with autism (AU) compared to age-matched controls including, siblings without ASD, typically developing (TD) controls, and children with other developmental disabilities, but not autism (DD). Plasma from 172 individuals (AU, n = 63, median age: 43 months; TD controls, n = 63, median age: 48 months; siblings, n = 25, median age: 61 months; and DD controls, n = 21, median age: 38 months) was analyzed by Western blot for the presence of IgG antibodies against protein extracts from specific regions of the human adult brain including the hypothalamus and thalamus. The presence of a approximately 52 kDa MW band, in the plasma of subjects with AU, was detected with a significantly higher incidence when compared to plasma from TD controls (29% vs. 8%, P = 0.0027 and 30% vs. 11%, P = 0.01, in the thalamus and hypothalamus, respectively). Reactivity to three brain proteins (42-48 kDa MW), in particular in the hypothalamus, were observed with increased incidence in 37% of subjects with AU compared to 13% TD controls (P = 0.004). Multiple brain-specific autoantibodies are present at significantly higher frequency in children with AU. While the potential role of these autoantibodies in AU is currently unknown, their presence suggests a loss of self-tolerance to one or more neural antigens during early childhood.

摘要

尽管自闭症谱系障碍(ASD)是根据行为参数进行诊断的,但多项研究报告了免疫系统异常,并提示自身免疫在ASD发病机制中可能发挥的作用。在本研究中,我们试图评估自闭症儿童(AU)血浆中脑特异性自身抗体的发生率,并与年龄匹配的对照组进行比较,这些对照组包括无ASD的兄弟姐妹、发育正常(TD)的对照组以及患有其他发育障碍而非自闭症(DD)的儿童。对172名个体的血浆(AU组,n = 63,中位年龄:43个月;TD对照组,n = 63,中位年龄:48个月;兄弟姐妹组,n = 25,中位年龄:61个月;DD对照组,n = 21,中位年龄:38个月)进行蛋白质印迹分析,以检测针对人类成脑特定区域(包括下丘脑和丘脑)蛋白质提取物的IgG抗体。与TD对照组的血浆相比,AU组受试者血浆中出现约52 kDa分子量条带的发生率显著更高(丘脑分别为29% 对8%,P = 0.0027;下丘脑为30% 对11%,P = 0.01)。在37%的AU组受试者中观察到对三种脑蛋白(42 - 48 kDa分子量)的反应性增加,尤其是在下丘脑,而TD对照组为13%(P = 0.004)。多种脑特异性自身抗体在AU儿童中的出现频率显著更高。虽然目前尚不清楚这些自身抗体在AU中的潜在作用,但它们的存在提示在幼儿期对一种或多种神经抗原的自身耐受性丧失。

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