Leukocyte cytokine expression is associated with severity of autism in children

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder with unknown etiology, high clinical heterogeneity and marked aberrations of the immune system. Evidence for an association between immune dysfunction and behavioral traits highlights the need for a study of the immune cell functional activity in order to search for pathogenesis mechanisms and potential targets for therapy at ASD. The purpose: to determine the expression levels of IL-1, IL-2, IL-4, IL-6, IL-10, IL-18, IFN and TNF in peripheral blood leukocytes of children with mild and severe ASD. The study included 81 children with ASD (77.8% boys) and 45 children with typical neurodevelopment (TDC, 71.1% boys). According to the Childhood Autism Rating Scale, 51 children (63.0%) had mild autistic symptoms (CARS score 32.01,5) and 30 children had severe ASD symptoms (CARS score 39.03,4). Cytokines expression in leukocytes was determined by quantitative PCR with SYBRGreen. The data were transformed using BoxCox transformation. The differences between groups were assessed by one-way ANOVA and Dunns test for multiple comparisons. In leukocytes of children with ASD, regardless of the severity, the expression of IL-1, IL-18 and IL-2, was significantly reduced compared to TDC. Moreover, in children with mild ASD, low expression of TNF, compared with TDC was found. In children with severe ASD, the expression of the main cytokine of Th1 IFN, was significantly increased, without an increased expression of an important cytokine of Treg IL-10. Activation of the Th1 adaptive immune response without compensation by cytokines of Treg, the number of which is reduced in ASD, can lead to increased inflammation, even in the central nervous system, and correlates with the severity of ASD clinical symptoms. Despite extensive immunological evidence suggesting immune system dysregulation, further research is required to clarify the relationship between immune system cell function and ASD pathology.