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Significant Changes in the Levels of Secreted Cytokines in Brains of Experimental Antiphospholipid Syndrome Mice

机译:实验性抗磷脂综合征小鼠脑中分泌细胞因子水平的显着变化

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摘要

Antiphospholipid syndrome (APS) is characterized by thromboses and neuropsychiatric manifestations possibly linked to brain inflammation. In order to examine the levels of proinflammatory and anti-inflammatory cytokines in experimental APS (eAPS) mice brains, we measured the levels of TNF-α, IFN-γ, and IL-10 in brain homogenates (cytosolic fractions) and in brain slices (secreted level) at 6, 15, and 24 weeks after immunization. We induced eAPS by immunization of Balb/c mice with β 2-glycoprotein I (β 2GPI), the major autoantigen in the disease and controls with adjuvant alone. We found increased levels of secreted TNF-α in eAPS mice for the entire experiment period. Cytosolic and secreted IL-10 and IFN-γ levels in eAPS mice were lower at 6 and 15 weeks and higher at 24 weeks after immunization. The results suggest that brain disease in APS is associated with significant and complex changes in proinflammatory and anti-inflammatory cytokines.
机译:抗磷脂综合症(APS)的特征在于可能与脑部炎症有关的血栓形成和神经精神病学表现。为了检查实验性APS(eAPS)小鼠大脑中促炎和抗炎细胞因子的水平,我们测量了脑匀浆(胞浆级分)和脑切片中TNF-α,IFN-γ和IL-10的水平。免疫后第6、15和24周(分泌水平)。我们通过用β2-糖蛋白I(β2GPI)免疫Balb / c小鼠来诱导eAPS,β2-糖蛋白I是该疾病中的主要自身抗原,仅用佐剂进行对照。我们发现在整个实验期间,eAPS小鼠中分泌的TNF-α含量增加。免疫后6和15周时,eAPS小鼠的胞质和分泌IL-10和IFN-γ水平较低,而在免疫后24周时较高。结果表明,APS中的脑部疾病与促炎和抗炎细胞因子的显着而复杂的变化有关。

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