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特发性炎性肌病中肌肉浸润淋巴细胞的主要TCR-αβ可变区和连接基因表达

Predominant TCR-alpha beta variable and joining gene expression by muscle-infiltrating lymphocytes in the idiopathic inflammatory myopathies.

作者信息

O'Hanlon T P, Dalakas M C, Plotz P H, Miller F W

机构信息

Laboratory of Molecular Immunology, Food and Drug Administration, Bethesda, MD 20892.

出版信息

J Immunol. 1994 Mar 1;152(5):2569-76.

PMID:8133064
Abstract

The idiopathic inflammatory myopathies (IIM) are a heterogeneous group of diseases in which autoreactive T cells are thought to play a pathogenetic role. We have determined the pattern of TCR-alpha beta gene expression by muscle-infiltrating lymphocytes within clinically and serologically defined groups of IIM patients. We utilized the PCR to study TCR V gene expression in muscle biopsies from nine polymyositis (PM) and eight dermatomyositis (DM) patients, all of whom had autoantibodies directed against histidyl-transfer RNA synthetase (anti-Jo-1 autoantibodies). While the TCR repertoire in DM patients was generally polyclonal, an oligoclonal profile characterized PM patients. Certain V gene families were predominantly expressed; V alpha 1 and V beta 6 gene families were detected in 82 and 91% of PM biopsies, respectively. TCR expression was characterized further by analyzing J gene usage from four PM patients expressing the V beta 6 gene. Sequence analysis of 40 independent recombinants (10 per patient) identified only seven V beta 6 clonotypes and restricted usage of the related J beta 2.1, -2.3, and -2.7 genes. These data, describing predominant TCR V and J gene usage by muscle-infiltrating lymphocytes in myositis patients, suggest that Ag-driven T cell responses may play a primary role in mediating some forms of the IIM.

摘要

特发性炎性肌病(IIM)是一组异质性疾病,其中自身反应性T细胞被认为起致病作用。我们已经确定了临床和血清学定义的IIM患者组中肌肉浸润淋巴细胞的TCR-αβ基因表达模式。我们利用聚合酶链反应(PCR)研究了9例多发性肌炎(PM)和8例皮肌炎(DM)患者肌肉活检中的TCR V基因表达,所有这些患者均有针对组氨酰转运RNA合成酶的自身抗体(抗Jo-1自身抗体)。虽然DM患者的TCR库通常是多克隆的,但PM患者的特征是寡克隆谱。某些V基因家族主要表达;Vα1和Vβ6基因家族分别在82%和91%的PM活检中被检测到。通过分析4例表达Vβ6基因的PM患者的J基因使用情况,进一步对TCR表达进行了表征。对40个独立重组体(每位患者10个)的序列分析仅鉴定出7种Vβ6克隆型,并限制了相关Jβ2.1、-2.3和-2.7基因的使用。这些描述了肌炎患者肌肉浸润淋巴细胞主要TCR V和J基因使用情况的数据表明,抗原驱动的T细胞反应可能在介导某些形式的IIM中起主要作用。

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