Saliva versus plasma cytokines as possible predictors of autism severity

Y. Filippova, A. Alekseeva, E. V. Devyatova, K. A. Rusakova, A. Burmistrova
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Abstract

The autism spectrum disorders (ASD) are now widely accepted as a pervasive, complex, heterogeneous neurodevelopmental disorders with multiple etiologies, subtypes, and developmental trajectories. There are no available and effective biomarkers for them. Immune dysfunction is seen as an important risk factor contributing to the neurodevelopmental deficit in ASD, and is signified, among other things, by an imbalance of cytokines in the brain and on the periphery. In recent years, saliva has been proposed as a biological material for diagnosing ASD, due to the accessibility and non-invasiveness of the method for its production. However, the question of whether salivary cytokine levels may be used as effective early biomarkers for autism requires further research, including saliva versus plasma/serum comparisons.Aim: a comparative analysis of the levels of cytokines: IL-6, IFNγ, TNFα, IL-1β, IL-4, IL-10, in saliva and blood plasma to identify possible markers of ASD and their severity in children.The study included 11 children with typical neurodevelopment (TDC) and 55 children with ASD, among whom 37 children had mild or moderate autism (according to CARS), and 18 children had severe autism. Samples of unstimulated mixed saliva and venous blood were simultaneously collected from all children. Salivary concentrations of cytokines: IL-6, IFNγ, TNFα, IL-1β, IL-4, IL-10 were determined by multiplex Luminex™ analysis. Plasma levels of cytokines were assessed by ELISA. Differences between groups were tested using the Kruskal-Wallis U-test with post-hoc Conover-Inman comparisons, between samples (saliva/ plasma) are using the Wilcoxon signed-rank test. The correlation between the concentrations of cytokines in plasma and saliva was determined using linear regression by the RMA method.In all examined groups, the levels of IL-6, IFNγ and IL-10 in saliva were significantly lower, and TNFα, IL-1β and IL-4 were higher than the corresponding levels of the same cytokines in plasma. Regardless of health/ disease status, no significant correlations were found between salivary and plasma cytokine levels in children. IL-1β levels were significantly lower and IL-10 levels were higher in the saliva of both groups of children with ASD compared with TDC. No significant differences in salivary cytokine concentrations were found between children with mild and severe ASD.Thus, salivary cytokines can be used as markers of ASD in children, but not the severity of the condition. The absence of correlations in the levels of some pro/anti-inflammatory cytokines between saliva and blood plasma may probably indicate a special immunological status of an ecological niche, the oral cavity.
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唾液和血浆细胞因子可能是自闭症严重程度的预测因子
自闭症谱系障碍(ASD)是一种普遍的、复杂的、异质性的神经发育障碍,具有多种病因、亚型和发育轨迹。目前还没有可用和有效的生物标志物。免疫功能障碍被认为是导致ASD神经发育缺陷的一个重要危险因素,除其他因素外,还表现为大脑和外周细胞因子的失衡。近年来,由于唾液生产方法的可及性和非侵入性,唾液被提出作为诊断ASD的生物材料。然而,唾液细胞因子水平是否可以作为自闭症有效的早期生物标志物的问题需要进一步的研究,包括唾液与血浆/血清的比较。目的:比较分析儿童唾液和血浆中IL-6、IFNγ、TNFα、IL-1β、IL-4、IL-10等细胞因子的水平,以确定儿童ASD的可能标志及其严重程度。该研究包括11名典型神经发育(TDC)儿童和55名ASD儿童,其中37名儿童患有轻度或中度自闭症(根据CARS), 18名儿童患有严重自闭症。同时采集所有患儿未受刺激的混合唾液和静脉血样本。唾液细胞因子浓度:IL-6、IFNγ、TNFα、IL-1β、IL-4、IL-10采用多重Luminex™分析。ELISA法检测血浆细胞因子水平。组间差异采用Kruskal-Wallis u检验和事后Conover-Inman比较,样本间(唾液/血浆)采用Wilcoxon符号秩检验。用RMA法线性回归测定血浆和唾液中细胞因子浓度的相关性。各组大鼠唾液中IL-6、ifn - γ、IL-10水平均显著低于各组大鼠唾液中IL-6、ifn - γ、IL-10水平,tnf - α、IL-1β、IL-4水平均高于各组大鼠血浆中相应水平。无论健康/疾病状况如何,儿童唾液和血浆细胞因子水平之间没有发现显著相关性。两组ASD患儿唾液中IL-1β水平显著低于TDC, IL-10水平显著高于TDC。轻度和重度ASD患儿的唾液细胞因子浓度无显著差异。因此,唾液细胞因子可以作为儿童自闭症谱系障碍的标志,但不能作为病情严重程度的标志。唾液和血浆中某些促炎/抗炎细胞因子的水平缺乏相关性可能表明口腔生态位的特殊免疫状态。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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