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首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Myelin basic protein-specific T lymphocytes proliferation and programmed cell death in demyelinating diseases.
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Myelin basic protein-specific T lymphocytes proliferation and programmed cell death in demyelinating diseases.

机译:脱髓鞘疾病中髓鞘碱性蛋白特异性T淋巴细胞增殖和程序性细胞死亡。

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摘要

A dynamic equilibrium between proliferation and programmed cell death (PCD) of auto-reactive T lymphocytes plays a pivotal role in the prevention of autoimmune diseases. We analyzed T lymphocytes myelin basic protein (MBP)-specific PCD and proliferation in demyelinating diseases. Results showed that MBP-specific PCD was significantly decreased in CD4+ and CD8+ T lymphocytes of progressive multifocal leukoencephalopathy (PML), not determined leukoencephalopathy (NDLE), and acute MS (AMS) patients compared to patients with stable MS (SMS) and healthy controls. MBP-specific proliferation/PCD rates were high in CD4+ T lymphocytes of PML, NDLE, and AMS patients, and in CD8+ T cells of PML and AMS individuals alone. Alterations of the balance between MBP-specific proliferation and PCD are present in demyelinating diseases and could play a major role in the pathogenesis of these diseases.
机译:自身反应性T淋巴细胞的增殖与程序性细胞死亡(PCD)之间的动态平衡在预防自身免疫性疾病中起着关键作用。我们分析了T淋巴细胞髓磷脂碱性蛋白(MBP)特异性PCD和脱髓鞘疾病中的增殖。结果显示,与稳定MS(SMS)和健康对照组相比,进行性多灶性白质脑病(PML),未确定的白质脑病(NDLE)和急性MS(AMS)患者的MB4特异性PCD显着降低。在PML,NDLE和AMS患者的CD4 + T淋巴细胞中,以及仅在PML和AMS患者的CD8 + T细胞中,MBP特异性增殖/ PCD率较高。 MBP特异性增殖与PCD之间平衡的改变存在于脱髓鞘疾病中,并且可能在这些疾病的发病机理中发挥重要作用。

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