Autism Research and Treatment Center, AL-Amodi Autism Research Chair, Department of Physiology, Faculty of Medicine, King Saud University, Riyadh, Saudi Arabia.
Brain Behav Immun. 2011 Oct;25(7):1393-8. doi: 10.1016/j.bbi.2011.04.006. Epub 2011 Apr 18.
Autoimmunity to brain may play an etiopathogenic role in autism. Osteopontin is a pro-inflammatory cytokine that has been shown to play an important role in various autoimmune neuroinflammatory diseases. Osteopontin induces IL-17 production by T-helper 17 lymphocytes, the key players in the pathogenesis of autoimmune disorders. Anti-osteopontin treatment reduces the clinical severity of some autoimmune neuroinflammatory diseases by reducing IL-17 production. We are the first to measure serum osteopontin levels, by ELISA, in 42 autistic children in comparison to 42 healthy-matched children. The relationship between serum osteopontin levels and the severity of autism, which was assessed by using the Childhood Autism Rating Scale (CARS), was also studied. Autistic children had significantly higher serum osteopontin levels than healthy controls (P<0.001). Increased serum osteopontin levels were found in 80.95% (34/42) of autistic children. Children with severe autism had significantly higher serum osteopontin levels than patients with mild to moderate autism (P=0.02). Moreover, serum osteopontin levels of autistic patients had significant positive correlations with CARS (P=0.007). In conclusions, serum osteopontin levels were increased in many autistic children and they were significantly correlated to the severity of autism. Further wide-scale studies are warranted to shed light on the etiopathogenic role of osteopontin in autism and to investigate its relation to IL-17 and brain-specific auto-antibodies, which are indicators of autoimmunity, in these patients. The therapeutic role of anti-osteopontin antibodies in amelioration of autistic manifestations should also be studied.
自身免疫脑可能在自闭症中起病因作用。骨桥蛋白是一种促炎细胞因子,已被证明在各种自身免疫性神经炎症性疾病中发挥重要作用。骨桥蛋白诱导辅助性 T 细胞 17 淋巴细胞(自身免疫性疾病发病机制中的关键细胞)产生白细胞介素-17。抗骨桥蛋白治疗通过减少白细胞介素-17 的产生,降低了一些自身免疫性神经炎症性疾病的临床严重程度。我们首次通过 ELISA 测量了 42 名自闭症儿童和 42 名健康儿童的血清骨桥蛋白水平。还研究了血清骨桥蛋白水平与自闭症严重程度之间的关系,自闭症严重程度通过儿童自闭症评定量表(CARS)进行评估。自闭症儿童的血清骨桥蛋白水平明显高于健康对照组(P<0.001)。80.95%(34/42)的自闭症儿童血清骨桥蛋白水平升高。自闭症严重程度较高的儿童血清骨桥蛋白水平明显高于自闭症轻度至中度的儿童(P=0.02)。此外,自闭症患者的血清骨桥蛋白水平与 CARS 呈显著正相关(P=0.007)。总之,许多自闭症儿童的血清骨桥蛋白水平升高,并且与自闭症的严重程度显著相关。需要进一步进行广泛的研究,以阐明骨桥蛋白在自闭症中的病因作用,并研究其与白细胞介素-17 和脑特异性自身抗体的关系,后者是这些患者自身免疫的指标。还应研究抗骨桥蛋白抗体在改善自闭症表现方面的治疗作用。