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首页> 外文期刊>The Journal of Clinical Investigation: The Official Journal of the American Society for Clinical Investigation >Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesis
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Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesis

机译:拉斯穆森脑炎的人源化小鼠模型支持免疫介导的假说

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摘要

Rasmussen's encephalitis (RE) is a chronic inflammatory brain disorder that causes frequent seizures and unilateral hemispheric atrophy with progressive neurological deficits. Hemispherectomy remains the only treatment that leads to seizure freedom for this refractory epileptic syndrome. The absence of an animal model of disease has been a major obstacle hampering the development of effective therapies. Here, we describe an experimental mouse model that shares several clinical and pathological features with the human disease. Immunodeficient mice injected with peripheral blood mononuclear cells from RE patients and monitored by video electroencephalography developed severe seizures of cortical origin and showed intense astrogliosis and accumulation of human IFN-gamma- and granzyme B-expressing T lymphocytes in the brain compared with mice injected with immune cells from control subjects. We also provide evidence for the efficacy of alpha 4 integrin blockade, an approved therapy for the treatment of multiple sclerosis and Crohn's disease, in reducing inflammatory markers associated with RE in the CNS. This model holds promise as a valuable tool for understanding the pathology of RE and for developing patient-tailored experimental therapeutics.
机译:拉斯穆森脑炎 (RE) 是一种慢性炎症性脑部疾病,可导致频繁癫痫发作和单侧半球萎缩,伴有进行性神经功能缺损。半球切除术仍然是导致这种难治性癫痫综合征无癫痫发作的唯一治疗方法。缺乏疾病的动物模型一直是阻碍有效疗法发展的主要障碍。在这里,我们描述了一种实验性小鼠模型,该模型与人类疾病具有多种临床和病理特征。注射来自RE患者的外周血单核细胞并通过视频脑电图监测的免疫缺陷小鼠发生皮质来源的严重癫痫发作,并显示出强烈的星形胶质增生和人IFN-γ和颗粒酶B表达T淋巴细胞的积累与注射来自对照受试者的免疫细胞的小鼠相比。我们还提供了α4整合素阻断(一种获批用于治疗多发性硬化症和克罗恩病的疗法)在减少中枢神经系统中与RE相关的炎症标志物方面的疗效的证据。该模型有望成为了解 RE 病理学和开发患者量身定制的实验疗法的宝贵工具。

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