首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Peripheral B cell depletion and central proinflammatory cytokine reduction following repeated intrathecal administration of rituximab in progressive Multiple Sclerosis
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Peripheral B cell depletion and central proinflammatory cytokine reduction following repeated intrathecal administration of rituximab in progressive Multiple Sclerosis

机译:在进行性多发性硬化症中反复鞘内注射利妥昔单抗后外周血B细胞耗竭和中枢促炎细胞因子减少

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摘要

B cells and/or the enhanced inflammatory milieu in the subarachnoid space are supposed to have a role in cortical pathology of progressive multiple sclerosis (PMS). The efficacy of intravenous rituximab to deplete circulating B cells is remarkable in MS, and its intrathecal delivery could target compartmentalized inflammation in PMS. We describe the central and peripheral effects of repeated intrathecal rituximab administrations in a patient with severe PMS. Peripheral CD20. + B cells were reduced, while oligoclonal bands were unaffected. Several central proinflammatory cytokines, and markers of neurodegeneration were markedly reduced. Central B cells modulation should be investigated in PMS.
机译:蛛网膜下腔中的B细胞和/或炎性环境增强被认为在进行性多发性硬化症(PMS)的皮质病理学中起作用。静脉注射利妥昔单抗消耗循环B细胞的功效在MS中非常显着,其鞘内递送可以靶向PMS中的区室性炎症。我们描述了在患有严重PMS的患者中反复鞘内注射利妥昔单抗的中枢和外周作用。外围CD20。 + B细胞减少,而寡克隆带不受影响。几种中枢促炎细胞因子和神经变性标记明显减少。中央B细胞的调制应在PMS中进行研究。

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