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乳癌患者转移淋巴结中T细胞受体β链互补决定区3谱型分析∗

张建波 吕晓东 宋巍 孙淼淼 于庆凯 冯稳 刘明阁 胡骏 房百俊

郑州大学学报(医学版)Issue(4):481-484,4.
郑州大学学报(医学版)Issue(4):481-484,4.DOI:10.13705/j.issn.1671-6825.2015.04.008

乳癌患者转移淋巴结中T细胞受体β链互补决定区3谱型分析∗

Analysis of complementarity determining region 3 repertoire of T cell re-ceptor β chain in metastatic lymph node from patients with breast cancer

张建波 1吕晓东 2宋巍 1孙淼淼 1于庆凯 1冯稳 1刘明阁 1胡骏 3房百俊4

作者信息

  • 1. 郑州大学附属肿瘤医院病理科 郑州 450003
  • 2. 郑州大学附属肿瘤医院中心实验室 郑州 450003
  • 3. 中山大学中山医学院微生物学教研室 广州 510089
  • 4. 郑州大学附属肿瘤医院血液科 郑州 450003
  • 折叠

摘要

Abstract

Aim: To analyze the specific repertoire skewing and amino acid sequences of the complementarity determi-ning region 3(CDR3) of T cell receptor(TCR) β chain in metastatic lymph node from patients with breast cancer. Methods:A total of 24 TCR β chain variable region(BV) subfamilies were amplified by RT-PCR, and the CDR3 lengths were analyzed with GeneScan method in lymph nodes from 2 patients with reactive hyperplasia and metastatic lymph nodes from 5 patients with breast cancer. Sequence analysis of the CDR3 region in monoclonal or oligoclonal expanded T cells was performed. Re-sults: There were only multiclonal expanded T cells in lymph nodes from patients with reactive hyperplasia, while there were monoclonal, oligoclonal, and multiclonal expanded T cells in metastatic lymph nodes from patients with breast cancer. TCR BV presented specific repertoire skewing in metastatic lymph node from patients with breast cancer, among which only 2-5 TCR BV subfamilies were identified. The monoclonal or oligoclonal expanded T cells had different CDR3 amino acid se-quences. Conclusion: There is specific repertoire skewing of TCR BV subfamilies in metastatic lymph nodes from patients with breast cancer. The amino acid sequences of CDR3 in different T cell clone proliferation are mostly different.

关键词

乳腺肿瘤/T细胞受体/互补决定区3

Key words

breast neoplasm/T cell receptor/complementarity determining region 3

分类

医药卫生

引用本文复制引用

张建波,吕晓东,宋巍,孙淼淼,于庆凯,冯稳,刘明阁,胡骏,房百俊..乳癌患者转移淋巴结中T细胞受体β链互补决定区3谱型分析∗[J].郑州大学学报(医学版),2015,(4):481-484,4.

基金项目

国家自然科学基金资助项目81370661 ()

河南省基础与前沿技术研究计划基金资助项目102300410038 ()

郑州大学学报(医学版)

OA北大核心CSTPCD

1671-6825

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