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特立氟胺可使抗 ANXA2 自身免疫性血小板减少症(APS)小鼠模型的抗焦虑作用正常化。 特立氟胺在抗 ANXA2 小鼠模型中的作用。

Teriflunomide normalizes anti-anxiety effect in anti-ANXA2 APS mice model teriflunomide in anti-ANXA2 mice model.

机构信息

Department of Neurology, 26744Sheba Medical Center, Ramat Gan, Israel.

Department of Neurology and Neurosurgery, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Lupus. 2022 Jun;31(7):855-863. doi: 10.1177/09612033221095150.

Abstract

Antiphospholipid syndrome (APS) affects the brain by both hypercoagulation and immunological mechanisms. APS is characterized by several autoantibodies binding to a thrombolytic complex including beta-2-glycoprotein I (β2-GPI) and annexin A2 (ANXA2). Teriflunomide, an oral drug for the treatment of multiple sclerosis (MS), has a cytostatic effect on B cells and is therefore a potential antibody-targeting treatment for APS. In this study, we assessed the effect of teriflunomide in two APS mouse models by inducing autoantibody formation against β2-GPI and ANXA2 in female BALB/c mice. The ANXA2 model displayed a behavioral change suggesting an anti-anxiety effect in open field and forced swim tests, early in the course of the disease. This effect was normalized following teriflunomide treatment. Conversely, behavioral tests done later during the study demonstrated depression-like behavior in the ANXA2 model. No behavioral changes were seen in the β2-GPI model. Total brain IgG levels were significantly elevated in the ANXA2 model but not in the teriflunomide treated group. No such change was noted in the brains of the β2-GPI model. High levels of serum autoantibodies were induced in both models, and their levels were not lowered by teriflunomide treatment. Teriflunomide ameliorated behavioral changes in mice immunized with ANXA2 without a concomitant change in serum antibody levels. These findings are compatible with the effect of teriflunomide on neuroinflammation.Teriflunomide ameliorated behavioral and brain IgG levels in mice immunized with ANXA2 without a concomitant change in serum antibody levels. These findings are compatible with an effect of teriflunomide on the IgG permeability to the brain and neuroinflammation.

摘要

抗磷脂综合征 (APS) 通过血栓形成和免疫机制影响大脑。APS 的特征是几种自身抗体与包括β2-糖蛋白 I (β2-GPI) 和膜联蛋白 A2 (ANXA2) 在内的溶栓复合物结合。特立氟胺是一种用于治疗多发性硬化症 (MS) 的口服药物,对 B 细胞具有细胞抑制作用,因此是 APS 的潜在抗体靶向治疗药物。在这项研究中,我们通过在雌性 BALB/c 小鼠中诱导针对β2-GPI 和 ANXA2 的自身抗体形成,在两种 APS 小鼠模型中评估了特立氟胺的作用。ANXA2 模型在疾病早期的开阔场和强迫游泳试验中显示出行为改变,提示具有抗焦虑作用。这种作用在特立氟胺治疗后得到了纠正。相反,在研究后期进行的行为测试显示 ANXA2 模型存在抑郁样行为。β2-GPI 模型未观察到行为变化。ANXA2 模型的总脑 IgG 水平显着升高,但特立氟胺治疗组没有升高。β2-GPI 模型的大脑没有发生这种变化。两种模型均诱导了血清自身抗体的高水平,特立氟胺治疗并未降低其水平。特立氟胺改善了用 ANXA2 免疫的小鼠的行为变化,而血清抗体水平没有变化。这些发现与特立氟胺对神经炎症的作用一致。特立氟胺改善了用 ANXA2 免疫的小鼠的行为和脑 IgG 水平,而血清抗体水平没有变化。这些发现与特立氟胺对 IgG 向大脑通透性和神经炎症的作用一致。

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