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杜兴氏肌营养不良症肌肉退化部位的特异性T细胞受体基因重排。

Specific T cell receptor gene rearrangements at the site of muscle degeneration in Duchenne muscular dystrophy.

作者信息

Gussoni E, Pavlath G K, Miller R G, Panzara M A, Powell M, Blau H M, Steinman L

机构信息

Department of Neurology and Neurological Sciences, Stanford University School of Medicine, CA 94305.

出版信息

J Immunol. 1994 Nov 15;153(10):4798-805.

PMID:7963545
Abstract

Mononuclear cells infiltrate degenerating muscles of Duchenne muscular dystrophy (DMD) patients. Using a quantitative PCR, we first characterized the T cells infiltrating muscle biopsies from six DMD patients. High levels of TCR V beta 2 transcripts were observed in DMD muscle tissue. TCR V beta 2 transcripts from seven DMD patients and five controls were sequenced, and the VDJ junctional region analyzed in 166 clones. One specific amino acid motif, RVSG, was found in the third complementary determining region (CDR3) of TCR V beta 2 chains in samples from five DMD patients, but not in controls. A specific immune reaction at the site of tissue degeneration may play an important role in the pathogenesis of DMD.

摘要

单核细胞浸润杜氏肌营养不良(DMD)患者的退化肌肉。我们首先使用定量PCR对6例DMD患者肌肉活检中浸润的T细胞进行了表征。在DMD肌肉组织中观察到高水平的TCR Vβ2转录本。对7例DMD患者和5例对照的TCR Vβ2转录本进行了测序,并对166个克隆中的VDJ连接区进行了分析。在5例DMD患者的样本中,在TCR Vβ2链的第三个互补决定区(CDR3)中发现了一个特定的氨基酸基序RVSG,而在对照中未发现。组织退化部位的特异性免疫反应可能在DMD的发病机制中起重要作用。

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