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首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Detection of skewed T-cell receptor V-beta gene usage in the peripheral blood of patients with multiple sclerosis.
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Detection of skewed T-cell receptor V-beta gene usage in the peripheral blood of patients with multiple sclerosis.

机译:多发性硬化症患者外周血中偏斜的T细胞受体V-β基因使用情况的检测。

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摘要

The ex vivo analysis of the T-cell receptor V-beta (TCRBV) gene usage by circulating T lymphocytes in Multiple Sclerosis (MS) patients may contribute to understanding disease pathogenesis. In the present study, TCRBV gene usage was analyzed in freshly collected unstimulated peripheral blood mononuclear cells (PBMC) isolated from 40 MS patients and 20 healthy controls. Nine patients presented abnormal repertoires, with expansion of one or more TCRBV segments. Among these patients, six presented expansion of TCRBV9 chain expression, three also having an expansion of TCRBV1, TCRBV11 and TCRBV22 segments. The most frequently observed TCRBV chain expansion, TCRBV9, was further analyzed and identified as polyclonal. Evaluation of clinical variables showed that median disease duration was shorter in patients with TCRBV gene expression abnormalities. Longitudinal evaluation of five patients with a skewed repertoire showed regression of expanded TCRBV chains expression to normal values. These data indicate that certain MS patients have abnormal TCRBV gene expression. Such abnormalities are caused by polyclonal expansions of T lymphocyte subpopulations that use the same TCRBV gene families, are unstable and preferentially observed early in the course of the disease.
机译:多发性硬化症(MS)患者中循环T淋巴细胞对T细胞受体V-beta(TCRBV)基因使用情况的离体分析可能有助于了解疾病的发病机理。在本研究中,分析了从40例MS患者和20例健康对照中分离出的新鲜收集的未刺激的外周血单核细胞(PBMC)中的TCRBV基因使用情况。 9名患者表现出异常的曲目,并扩展了一个或多个TCRBV片段。在这些患者中,有6位患者表现出TCRBV9链表达的扩展,其中3位患者也表现出TCRBV1,TCRBV11和TCRBV22段的扩展。进一步分析了最常见的TCRBV链扩展TCRBV9,并将其鉴定为多克隆的。临床变量的评估表明,患有TCRBV基因表达异常的患者的中位病程较短。纵向评估的五名患者的曲目库显示扩展的TCRBV链表达回归正常值。这些数据表明某些MS患者的TCRBV基因表达异常。这种异常是由使用相同TCRBV基因家族的T淋巴细胞亚群的多克隆扩增引起的,是不稳定的,并且在疾病过程的早期优先观察到。

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