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慢性炎症性脱髓鞘性多发性神经病和血管炎性神经病中腓肠神经T细胞受体Vβ基因的使用情况

Sural nerve T-cell receptor Vbeta gene utilization in chronic inflammatory demyelinating polyneuropathy and vasculitic neuropathy.

作者信息

Bosboom W M, Van den Berg L H, Mollee I, Sasker L D, Jansen J, Wokke J H, Logtenberg T

机构信息

Department of Neurology of the Rudolf Magnus Institute for Neurosciences, The Netherlands.

出版信息

Neurology. 2001 Jan 9;56(1):74-81. doi: 10.1212/wnl.56.1.74.

Abstract

OBJECTIVE

To investigate the utilization of T-cell receptor (TCR) variable (V) regions in infiltrates of sural nerve biopsies of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) and vasculitic neuropathy.

BACKGROUND

The presence of infiltrating T lymphocytes in sural nerve biopsies may suggest a T cell-mediated immune mechanism in the pathogenesis of CIDP and vasculitic neuropathy.

PATIENTS AND METHODS

The utilization of TCR Vbeta regions in sural nerves of 13 patients with CIDP and five patients with vasculitic neuropathy was determined by immunohistochemistry, reverse-transcription PCR, and nucleotide sequence analysis. These techniques were also applied in four patients with chronic idiopathic axonal polyneuropathy (CIAP) who acted as noninflammatory controls, and in five autopsy controls.

RESULTS

The TCR Vbeta utilization of infiltrating T cells in sural nerves of patients with CIDP, vasculitic neuropathy, and noninflammatory controls is heterogeneous. A dominant TCR Vbeta utilization was not found in any of the patients or controls.

CONCLUSION

There is no evidence for the presence of clonally expanded T cells in sural nerves of patients with CIDP and vasculitic neuropathy.

摘要

目的

研究慢性炎性脱髓鞘性多发性神经病(CIDP)和血管炎性神经病患者腓肠神经活检浸润物中T细胞受体(TCR)可变(V)区的利用情况。

背景

腓肠神经活检中浸润性T淋巴细胞的存在可能提示CIDP和血管炎性神经病发病机制中存在T细胞介导的免疫机制。

患者和方法

通过免疫组织化学、逆转录聚合酶链反应和核苷酸序列分析,确定13例CIDP患者和5例血管炎性神经病患者腓肠神经中TCR Vβ区的利用情况。这些技术也应用于4例慢性特发性轴索性多发性神经病(CIAP)患者(作为非炎性对照)和5例尸检对照。

结果

CIDP患者、血管炎性神经病患者和非炎性对照患者腓肠神经中浸润性T细胞的TCR Vβ利用情况是异质性的。在任何患者或对照中均未发现优势TCR Vβ利用情况。

结论

没有证据表明CIDP和血管炎性神经病患者的腓肠神经中存在克隆性扩增的T细胞。

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