Morris Christina M, Zimmerman Andrew W, Singer Harvey S
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Pediatr Neurol. 2009 Oct;41(4):288-90. doi: 10.1016/j.pediatrneurol.2009.04.014.
Autoimmune hypotheses for autism include in utero transplacental exposure to maternal antibodies and acquired postnatal insults. Previous work demonstrated that some mothers of children with autistic disorder have specific antibodies against human fetal brain that differentiate them from mothers with typical children. In the present study, Western immunoblotting was used to determine whether children with autistic spectrum disorders (n = 29) have serum reactivity against human fetal brain that differs from that of controls (n = 14). There was no significant difference in reactivity, corrected for serum immunoglobulin G content and brain actin content and with special attention to reactive bands at 36, 39, 61, and 73 kDa, between autistic children and normal control subjects. Thus, in contrast to mothers, antibody reactivity against human fetal brain as measured in children ages 3-12 years does not appear to be a useful biomarker for autism.
自闭症的自身免疫假说包括子宫内经胎盘接触母体抗体以及出生后获得性损伤。先前的研究表明,一些自闭症谱系障碍儿童的母亲具有针对人类胎儿大脑的特异性抗体,这使她们有别于正常儿童的母亲。在本研究中,采用蛋白质免疫印迹法来确定自闭症谱系障碍儿童(n = 29)血清与人胎儿大脑的反应性是否与对照组(n = 14)不同。校正血清免疫球蛋白G含量和脑肌动蛋白含量,并特别关注36、39、61和73 kDa处的反应条带后,自闭症儿童与正常对照受试者之间的反应性没有显著差异。因此,与母亲不同,在3至12岁儿童中检测到的针对人类胎儿大脑的抗体反应性似乎并非自闭症的有用生物标志物。