TH1/Treg ratio may be a marker of autism in children with immune dysfunction

心理学 自闭症 FOXP3型 细胞因子 细胞毒性T细胞 CD8型 背景(考古学) 免疫系统 促炎细胞因子 T细胞 T辅助细胞 发展心理学 免疫学 生物 炎症 医学 遗传学 古生物学 体外
作者
Zu-Qing Nie,Dong‐Wook Han,Kun Zhang,Meng Li,Ho‐Keun Kwon,Sin‐Hyeog Im,Li Xu,Jichun Yang,Zhiwei Li,Xinwei Huang,Jie Wen,Shujun Yang,F Yin,Chen‐Yang Shen,Paul Ashwood,Chuanyuan Kang,Xia Cao
出处
期刊:Research in Autism Spectrum Disorders [Elsevier BV]
卷期号:101: 102085-102085 被引量:11
标识
DOI:10.1016/j.rasd.2022.102085
摘要

Evidence suggests a link between autism spectrum disorder (ASD), behavioral symptoms in the context of ASD, and presence of an altered immune function. Several studies have highlighted differences in T-lymphocyte subpopulations, their activation status, and their response to stimulation in children and adults with ASD. These T cell abnormalities have often been associated with more impaired behaviors. However, few studies have attempted to address whether T cell subsets have the potential to serve as biomarkers in ASD. Moreover, although many studies have been performed in Western populations, few (if any) have been performed in Asian populations in mainland China. In this study we used intracellular cytokine flow cytometry to assess the frequencies of CD4+ T-cell subpopulations (T-helper (TH) 1, TH2, TH17, Foxp3+ regulatory T cells (Treg) as well as CD8+, subpopulations of T cytotoxic (TC) 1, TC2, and TC17 in 82 children with ASD and 50 healthy typical developing children from the Second Affiliated Hospital of Kunming Medical University of Yunnan province. To further elucidate immune status cytokine levels were also measured in the plasma and serum using a bead-based cytokine assay. Our results showed that the frequency of circulating Treg cells and the levels of active TGF-β1 in plasma were lower in children with ASD than in healthy controls. In contrast, the frequencies of TH1, TH2, TH17 and TC1 cells were increased. Proinflammatory cytokine levels of TNF-α, IL-4, IL-5 and IL-17A were higher in the plasma of children with ASD compared to typical controls. We also found an association between the severity of behavior impairments in ASD children and altered immune responses as measured using the effector T cell responses and regulatory responses (using Teff/Treg ratios). Higher the Teff/Treg ratios, were associated with more severe problematic behavioral symptoms. Further, the potential biomarker relevance of Teff/Treg ratio was evaluated by the receiver operating characteristics curve. Data suggests that high TH1/Treg cell ratios could also be used as a potential marker for the diagnosis of children with ASD. Overall, our data suggest an imbalance in inflammatory and regulatory immune responses in ASD. Ratios of inflammatory/regulatory cells or cell frequencies such as Teff/Treg cells may be useful biomarkers for children with ASD with immune dysfunction.
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