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Cerebrospinal fluid and serum cytokine profiling to detect immune control of infectious and inflammatory neurological and psychiatric diseases

机译:脑脊液和血清细胞因子谱分析,以检测对感染性和炎症性神经病和精神病的免疫控制

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The present study aimed at profiling inflammatory cytokines for neurological and psychiatric diseases. A total of 86 patients with meningitis, multiple sclerosis, tension-type headache, idiopathic facial nerve palsy (IFNP), affective and schizophrenic disorders were tested for both, serum and cerebrospinal fluid (CSF) using a multiplexed cytokine ELISA for IFN-γ, TNF-α, IL-1β, IL-2, IL-4, IL-5, IL-8/CXCL8, IL-10, IL12p70, IL-13 and IL-17.Cases with viral and bacterial meningitis had unequivocally higher cytokine concentrations in the CSF when compared with serum. Bacterial meningitis was unique by extremely elevated IL-17, TNF-α and IL-1β, indicating a plethora of inflammatory pathways, selectively activated in the CSF. In relapsing multiple sclerosis, IFN-γ and IL-10 were elevated in both, serum and CSF, but IL-12p70, IL-5, IL-13, and TNF-α were more prominent in serum than in CSF. Qualitatively similar biomarker patterns were detected in patients with idiopathic facial nerve palsy and tension-type cephalgia. Affective and schizophrenic disorders clearly present with an inflammatory phenotype in the CSF and also serum, the cytokines determined were in general higher in schizophrenia. Except IFN-γ, schizophrenic patients had higher IL-12p70 and a trend of higher IL-10 and IL-13 in serum suggesting a more prominent TH2-type counter regulatory immune response than in affective disorders. These differences were also mirrored in the CSF. Elevated IL-8 appears to be the most sensitive marker for inflammation in the CSF of all diseases studied, whereas TNF-α was restricted to peripheral blood. With the exception of IL-8, all but viral and bacterial meningitis, studied, displayed higher means of elevated lymphokine concentrations in the serum than in the CSF. This observation supports the concept of immunological crosstalk between periphery and intrathecal immunity in neurological and psychiatric diseases.
机译:本研究的目的是分析神经和精神疾病的炎症细胞因子。使用多重细胞因子ELISA进行IFN-γ检测,对86例脑膜炎,多发性硬化症,紧张型头痛,特发性面神经麻痹(IFNP),情感和精神分裂症患者的血清和脑脊液(CSF)进行了测试, TNF-α,IL-1β,IL-2,IL-4,IL-5,IL-8 / CXCL8,IL-10,IL12p70,IL-13和IL-17伴有病毒和细菌性脑膜炎的病例细胞因子明显升高与血清比较时脑脊液中的浓度。细菌性脑膜炎的独特之处在于IL-17,TNF-α和IL-1β的极度升高,表明存在过多的炎症途径,并在CSF中被选择性激活。在复发性多发性硬化症中,血清和脑脊液中的IFN-γ和IL-10均升高,但血清中IL-12p70,IL-5,IL-13和TNF-α比CSF中更为突出。在特发性面神经麻痹和紧张型头疼患者中检测到定性相似的生物标志物模式。情感和精神分裂症明显表现为CSF和血清中的炎症表型,在精神分裂症中确定的细胞因子一般较高。除IFN-γ以外,精神分裂症患者的血清中IL-12p70较高,并且IL-10和IL-13的趋势较高,这表明与情感障碍相比,TH2型抗调节免疫反应更为突出。这些差异也反映在CSF中。在研究的所有疾病中,升高的IL-8似乎是CSF中炎症最敏感的标志物,而TNF-α仅限于外周血。除IL-8外,除病毒性和细菌性脑膜炎外,所有研究均显示血清中淋巴因子浓度升高的方法比CSF中高。该观察结果支持神经和精神疾病中外周和鞘内免疫之间的免疫串扰概念。

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