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白细胞介素-12对肺癌患者区域淋巴结淋巴细胞与白细胞介素-2进行体外培养的影响。

Effects of interleukin-12 on in vitro culture with interleukin-2 of regional lymph node lymphocytes from lung cancer patients.

作者信息

Hanagiri T, Takenoyama M, Yoshimatsu T, Hirashima C, Yoshino I, Nakanishi K, Nagashima A, Nomoto K, Yasumoto K

机构信息

Department of Surgery II, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

Cancer Immunol Immunother. 1996 Oct;43(2):87-93. doi: 10.1007/s002620050307.

Abstract

In the present study, we carried out a functional analysis of regional lymph node lymphocytes (RLNL) from patients with lung cancer after in vitro activation by interleukin-2 (IL-2) and interleukin-12 (IL-12). IL-12 (100 U/ml) enhanced both the proliferation and cytotoxic activity of RLNL in a culture with low doses of IL-2 (5-10 JRU/ml). After comparing an RLNL culture with a low dose of IL-2 alone, a higher proportion of CD8+ cells and CD56+ cells and a lower proportion of CD4+ cells were found in the culture with both IL-12 and a low dose of IL-2. Such a combination of the cytokines effectively activated RLNL in terms of the expression of IL-2 receptors. In the culture condition of IL-12 and a low dose of IL-2, a synergistic effect was observed in the production of such cytokines as interferon gamma, tumor necrosis factor alpha (TNF alpha), and TNF beta, as well as in tumor cytotoxicity. However, the addition of IL-12 inhibited the cytotoxicity of RLNL in the culture with a high dose of IL-2 (100 JRU/ml). This inhibition is considered to be partially due to the endogenous production of TNF alpha by lymphocytes, because the neutralization of TNF alpa bioactivity partially restored the cytotoxic activities of RLNL. Furthermore, in the presence of hydrocortisone, IL-12 synergistically enhanced the cytotoxic activity of RLNL cultured with a high dose of IL-2. These results provide useful information about the improvement of adoptive immunotherapy against cancer using RLNL.

摘要

在本研究中,我们对肺癌患者的区域淋巴结淋巴细胞(RLNL)进行了功能分析,这些淋巴细胞在体外经白细胞介素-2(IL-2)和白细胞介素-12(IL-12)激活。IL-12(100 U/ml)在低剂量IL-2(5-10 JRU/ml)培养条件下增强了RLNL的增殖和细胞毒性活性。在将RLNL单独用低剂量IL-2培养的情况进行比较后发现,在同时添加IL-12和低剂量IL-2的培养物中,CD8+细胞和CD56+细胞的比例较高,而CD4+细胞的比例较低。就IL-2受体的表达而言,这种细胞因子组合有效地激活了RLNL。在IL-12和低剂量IL-2的培养条件下,在干扰素γ、肿瘤坏死因子α(TNFα)和TNFβ等细胞因子的产生以及肿瘤细胞毒性方面观察到了协同效应。然而,添加IL-12会抑制RLNL在高剂量IL-2(100 JRU/ml)培养物中的细胞毒性。这种抑制被认为部分归因于淋巴细胞内源性产生TNFα,因为中和TNFα的生物活性可部分恢复RLNL的细胞毒性活性。此外,在存在氢化可的松的情况下,IL-12协同增强了用高剂量IL-2培养的RLNL的细胞毒性活性。这些结果为利用RLNL改进癌症过继性免疫疗法提供了有用信息。

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