Li X, Zhang X, Zhang Y
Immunology Research Unit, Suzhou Medical College.
Zhonghua Yi Xue Za Zhi. 1997 Feb;77(2):111-4.
To study the specific expansion method of human gamma delta T cell and the molecular mechanism against tumor cells.
The peripheral blood mononuclear cells were co-cultured with XG-7 cells as stimulating cells and activated for the expansion of gamma delta T cells. Immunophonotype was analysed by IIFA and FACS. The cytotoxicity of gamma delta T cell against tumor cells was measured by 51Cr four hour release assay.
When this novel culture system was used, gamma delta T cells mainly expressing V gamma 9/V delta 2 encoded TCR were selected and expanded rapidly from 4.8 +/- 3.4% to 46.2 +/- 8.3%. With exogenous interleukin-2, gamma delta T cells were expanded in large quantity 10(10) within 3 weeks. gamma delta T cells mediated strong cytotoxic activity to different tumor cells including K562, Daudi, XG-7 cell lines, but no cytotoxic activity to normal cells was observed. XG-7 cells expressed HSP molecules and anti-HSP in mAB blocked the proliferation of gamma delta T cells.
The method shows unique biological properties: brief, rapid, well-repeating and wide cytotoxic activity against tumor cells. So gamma delta T cells are of value in tumor adoptive immunotherapy.
研究人γδT细胞的特异性扩增方法及其抗肿瘤细胞的分子机制。
将外周血单个核细胞与XG-7细胞作为刺激细胞共培养,以激活γδT细胞进行扩增。通过间接免疫荧光分析(IIFA)和流式细胞术(FACS)分析免疫表型。采用51Cr四小时释放试验检测γδT细胞对肿瘤细胞的细胞毒性。
使用这种新型培养系统时,主要表达Vγ9/Vδ2编码的TCR的γδT细胞被筛选并迅速扩增,从4.8±3.4%增至46.2±8.3%。在外源性白细胞介素-2作用下,γδT细胞在3周内大量扩增至10(10)。γδT细胞对包括K562、Daudi、XG-7细胞系在内的不同肿瘤细胞介导强烈的细胞毒性活性,但对正常细胞未观察到细胞毒性活性。XG-7细胞表达热休克蛋白(HSP)分子,单克隆抗体(mAB)中的抗HSP可阻断γδT细胞的增殖。
该方法显示出独特的生物学特性:简便、快速、重复性好且对肿瘤细胞具有广泛的细胞毒性活性。因此,γδT细胞在肿瘤过继性免疫治疗中具有价值。