t细胞生长因子活化的外周血淋巴细胞中CD8+CD11b−细胞对胃癌患者抗肿瘤活性的抑制作用

T. Ebihara, N. Sakai, S. Koyama
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引用次数: 8

摘要

为了证实淋巴因子激活抑制(LAS)效应细胞的表型特征,我们从7例胃癌患者(4例不可切除癌和3例可切除癌)和3例健康对照的t细胞生长因子(TCGF)激活的外周血淋巴细胞(PBL)中分离出CD8+CD11b -和CD8 - CD11b -细胞。3例不可切除癌患者和1例可切除癌患者的CD8+CD11b−细胞均显示LAS细胞活性。然而,在健康对照的CD8+CD11b−细胞中未观察到LAS细胞活性。此外,来自癌症患者和对照组的CD8 - CD11b -细胞亚群均未表达任何抑制活性。这些事实清楚地表明,至少在晚期癌症患者中,负责抑制细胞介导的抗肿瘤免疫的细胞群存在于CD8+CD11b−t细胞中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Suppression by sorted CD8+CD11b− cells from T-cell growth factor-activated peripheral blood lymphocytes on cytolytic activity against tumour in patients with gastric carcinoma

To confirm the phenotypic characteristics of lymphokine-activated suppressor (LAS)effector cells, we isolated CD8+CD11b and CD8CD11b cells from T-cell growth factor (TCGF)-activated peripheral blood lymphocytes (PBL) in 7 patients with gastric carcinoma (4 non-resectable and 3 resectable carcinoma) and 3 healthy controls. Sorted CD8+CD11b cells from 3 of the patients with non-resectable carcinoma and from 1 of the patients with resectable carcinoma showed LAS cell activity. However, the LAS cell activity could not be observed in CD8+CD11b cells from healthy controls. In addition, a sorted CD8CD11b subset of cells from both cancer patients and control did not express any suppressive activity. These facts clearly show that the cell populations responsible for suppression of cell-mediated antitumour immunity reside within CD8+CD11b T-cells, at least in patients with advanced carcinoma.

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