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利用基因扫描分析TCR Vβ亚家族的CDR3长度方法检测T细胞克隆性 被引量:42

T CELL CLONALITY IDETIFICATION USING GENESCAN BY CDR3 SIZE OF T CELL RECEPTOR Vβ GENE
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摘要 分析了健康人、T-ALL外周血及T细胞株Molt-4和Jurkat中TCRVβT细胞的表达和克隆性。应用RT-PCR扩增TCRVβ24个亚家族的CDR3,并经基因扫描和序列分析确定T细胞克隆性。结果表明健康人表达除Vβ20外的多克隆T细胞;T-ALL仅表达3~4个Vβ亚家族T细胞;部分呈寡克隆性;Molt-4和Jurkat分别表达Vβ2和Vβ8单克隆T细胞。T-ALL中存在克隆性生长T细胞。该方法是检测T细胞克隆性的敏感和精确的方法。  cell clonality and T cell receptor(TCR) Vβ subfamily expression in peripheral blood of health and TALL cases or T cell line Molt4 and Jurkat cells were analyzed. The complementarity determining region 3(CDR3) of TCR 24 Vβ subfamily genes was amplificated using RTPCR, the products were further studied by genescan and sequencing analysis for identification of T cell clonality. Besides Vβ20, the expression of all subfamily TCR Vβ polyclonal T cells were found in normal cases. But only some Vβ subfamily T cells were expressed in 2 cases with TALL, and the oligoclonal T cell could found in some subfamily of TCR Vβ. Molt4 and Jurkat cells expressed only Vβ2 or Vβ8 subfamily and showed monoclone T cell in PCR products. It is a sensitive and exact method to identify T cell clonality. T cell clonal expansion may be found in TALL.
出处 《中国免疫学杂志》 CAS CSCD 北大核心 1998年第1期48-50,共3页 Chinese Journal of Immunology
关键词 基因扫描 T细胞 CDR3长度 克隆性 白血病 TCR Vβ gene Complementarity determining region 3(CDR3) Genescan T cell clonality Leukemia
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参考文献1

  • 1Wilson R K,Immunol Rev,1988年,101卷,149页

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