[JC病毒基因改变可能与进行性多灶性白质脑病有关]。

No to shinkei = Brain and nerve Pub Date : 2007-02-01
Yoshiaki Yogo, Chie Sugimoto, Huai-Ying Zheng, Tadaichi Kitamura
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引用次数: 0

摘要

进行性多灶性脑白质病(PML)是一种发生在胎儿中枢神经系统的脱髓鞘疾病。PML曾经是一种罕见的疾病,但现在在艾滋病(获得性免疫缺陷综合征)患者中相对常见。患者的免疫状态是PML发病的重要因素。然而,致病因子的遗传变化也可能参与疾病的发生和进展。可能与PML相关的主要遗传变化包括调控区重排和VP1环突变。这两种变化已被确定为通常发生在PML患者脑和脑脊液中的JCV (JCvirus) dna中的遗传变化。尽管尚不清楚这些变化如何参与PML的发病机制,但越来越多的证据表明VP1环突变与PML的进展有关。在这里,我们概述了这些遗传变化的研究(主要是我们自己进行的研究)。
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[Genetic changes in JC virus possibly associated with progressive multifocal leukoencephalopathy].

Progressive multifocal leukoencephalopathy (PML) is a fetal demyelinating disease in the central nervous system. PML was once a rare disease, but it is now relatively common among AIDS (acquired immunodeficiency syndrome) patients. The immunological state of patients mainly contributes to the pathogenesis of PML. Genetic changes of the etiological agent, however, may also be involved in the development and progression of the disease. The major genetic changes possibly associated with PML include the regulatory region rearrangement and the VP1 loop mutation. Both changes have been identified as genetic changes usually occurring in JCV (JCvirus) DNAs from the brain and cerebrospinal fluid of PML patients. Although it remained to be clarified how these changes are involved in the pathogenesis of PML, accumulating evidence suggests that the VP1 loop mutation is associated with the progression of PML. Here we overview studies (mainly those performed by ourselves) on these genetic changes.

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[Metabolic myopathy]. [Myasthenia gravis]. [Myasthenia gravis]. [Genetic changes in JC virus possibly associated with progressive multifocal leukoencephalopathy]. [Neuropathology of progressive multifocal leukoencephalopathy].
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