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源自肿瘤引流淋巴结的人胃癌特异性T细胞。

Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.

作者信息

Stulle K, Vollmers H P, Marquardt P, Müller-Hermelink H K

机构信息

Pathologisches Institut, Universität Würzburg, Germany.

出版信息

Br J Cancer. 1994 Dec;70(6):1053-9. doi: 10.1038/bjc.1994.448.

Abstract

In this paper we investigate the reactivity pattern of T cells from stomach carcinoma patients against autologous tumour cells. T cells obtained from the tumour environment, tumour-draining lymph nodes and peripheral blood were cloned in 78 patients with stomach cancer and anti-tumour cytotoxic T lymphocytes (CTLs) precursor frequencies were assessed in each sample by using limiting dilution analysis. When tumour-specific CTLs were tested for specific T-cell killing by using only low doses of Interleukin 2 (100 U ml-1), a moderate rate of proliferation frequency of T cells (0.047) and specific cytotoxicity (12%) were observed in lymph node populations. When both IL-2 and autologous tumour cells in mixed lymphocyte tumour cultures (MLTCs) were used for stimulation, a dramatic increase in number (0.1) and in specific lytic activity (46%) could be measured. No effect or specific activity to tumour cells was observed with peripheral blood lymphocytes and tumour-infiltrating lymphocytes.

摘要

在本文中,我们研究了胃癌患者T细胞对自体肿瘤细胞的反应模式。从肿瘤环境、引流肿瘤的淋巴结和外周血中获取T细胞,对78例胃癌患者的T细胞进行克隆,并通过有限稀释分析评估每个样本中抗肿瘤细胞毒性T淋巴细胞(CTL)前体频率。当仅使用低剂量白细胞介素2(100 U/ml)检测肿瘤特异性CTL的特异性T细胞杀伤时,在淋巴结群体中观察到T细胞的适度增殖频率(0.047)和特异性细胞毒性(12%)。当在混合淋巴细胞肿瘤培养物(MLTC)中同时使用白细胞介素2和自体肿瘤细胞进行刺激时,可以检测到数量(0.1)和特异性裂解活性(46%)的显著增加。在外周血淋巴细胞和肿瘤浸润淋巴细胞中未观察到对肿瘤细胞的作用或特异性活性。

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