首页> 外文期刊>Infection and immunity >In Vitro Expansion of T-Cell-Receptor Vα2.3+ CD4+ T Lymphocytes in HLA-DR17(3), DQ2+ Individuals upon Stimulation withMycobacterium tuberculosis
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In Vitro Expansion of T-Cell-Receptor Vα2.3+ CD4+ T Lymphocytes in HLA-DR17(3), DQ2+ Individuals upon Stimulation withMycobacterium tuberculosis

机译:结核分枝杆菌刺激后HLA-DR17(3),DQ2 +个体中T细胞受体Vα2.3+ CD4 + T淋巴细胞的体外扩增

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The T-cell receptor (TCR) Vα/β gene product expression upon in vitro stimulation with mycobacteria was investigated to assess whether T-cell proliferation was associated with any specific TCR V gene usage. T-cell-enriched populations from peripheral blood ofMycobacterium bovis BCG-vaccinated healthy blood donors were stimulated in vitro with live or killed M. tuberculosis or with a soluble extract thereof. TCR Vα/β repertoire analysis of reactive CD4+ and CD8+ T cells revealed a selective HLA-DR17(3), DQ2-restricted expansion of Vα2.3+ CD4+ T cells upon stimulation with live M. tuberculosis or its soluble extract. Third-complementarity-determining-region (CDR3) length analysis of the expanded Vα2.3+ T cells indicated an oligoclonal pattern with short CDR3 lengths in six of seven HLA-DR17(3), DQ2+individuals tested. In addition, Vα/Vβ repertoire analysis of T lymphocytes from a DR17(3), DQ2+ donor before and after BCG vaccination revealed that positivity of skin test reactivity was associated with expansion of Vα2.3+ CD4+ T lymphocytes with preferential use of a short CDR3 peak length after in vitro stimulation. Separation of M. tuberculosis soluble extract by fast protein liquid chromatography (FPLC) purification indicated that fractions corresponding to molecular masses of 60 to 70 and 15 to 25 kDa were particularly effective in eliciting Vα2.3+ CD4+ T-cell expansion.
机译:研究了用分枝杆菌体外刺激后的T细胞受体(TCR)Vα/β基因产物表达,以评估T细胞增殖是否与任何特定的TCR V基因使用相关。用活或杀死的 M体外刺激牛分枝杆菌BCG接种的健康献血者外周血中富集T细胞的细胞。结核病或其可溶性提取物。对反应性CD4 + 和CD8 + T细胞的TCRVα/β库分析显示了选择性的HLA-DR17(3),DQ2限制了Vα2.3的扩增活 M刺激后+ + CD4 + T细胞。结核病或其可溶性提取物。扩展的Vα2.3 + T细胞的第三互补决定区(CDR3)长度分析表明,在七个HLA-DR17(3)中的六个中,CDR3长度短的寡克隆模式,DQ2 + 个人进行了测试。此外,在接种卡介苗之前和之后,对来自DR17(3),DQ2 + 供体的T淋巴细胞的Vα/Vβ成分分析表明,皮肤试验反应性的阳性与Vα2.3 + CD4 + T淋巴细胞,体外刺激后优先使用较短的CDR3峰长。 M的分离。快速蛋白质液相色谱(FPLC)纯化方法分离的结核病可溶性提取物表明,对应于60至70和15至25 kDa分子量的级分在诱发Vα2.3 + CD4 < sup> + T细胞扩增。

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