Kessler R, Dumont S, Weitzenblum E, Poindron P
Department of Immunology, Immunopharmacology and Pathology, University Louis Pasteur, Strasbourg, France.
Respiration. 1998;65(5):363-8. doi: 10.1159/000029296.
The aim of our study was to determine whether macrophages from lung cancer patients could acquire antitumoral properties in an in vitro model.
We isolated macrophages from bronchoalveolar lavages performed in two groups of patients: patients with lung cancer and patients with lung infection. All patients were smokers. We used the inhibition of incorporation of 3H-thymidine by U937 tumoral cells as an in vitro cytostatic assay.
When stimulated by gamma interferon, alveolar macrophages either from lung cancer patients or from patients with lung infection induced cytostasis of proliferating U937 tumoral cells. This effect could be reproduced by using the supernatants of cultures of activated macrophages. When using optimal doses, gamma interferon showed an increased activity as compared with lipopolysaccharide. The combination of these two compounds was no more effective than gamma interferon alone in cancer patients. A macrophage/U937 tumoral cell ratio of 1/1 was sufficient to achieve a near-maximal cytostatic effect.
Our results demonstrate that it is possible to activate, in vitro, alveolar macrophages from lung cancer patients by stimulation with gamma interferon. These macrophages acquire antiproliferative properties against a sensitive tumoral cell line.
我们研究的目的是确定肺癌患者的巨噬细胞在体外模型中是否能够获得抗肿瘤特性。
我们从两组患者进行的支气管肺泡灌洗中分离巨噬细胞:肺癌患者和肺部感染患者。所有患者均为吸烟者。我们将U937肿瘤细胞对³H-胸腺嘧啶掺入的抑制作用用作体外细胞生长抑制试验。
当受到γ干扰素刺激时,来自肺癌患者或肺部感染患者的肺泡巨噬细胞均可诱导增殖的U937肿瘤细胞发生细胞生长抑制。使用活化巨噬细胞培养上清液可重现此效应。使用最佳剂量时,γ干扰素与脂多糖相比活性增强。在癌症患者中,这两种化合物的组合并不比单独使用γ干扰素更有效。巨噬细胞与U937肿瘤细胞的比例为1/1足以实现接近最大的细胞生长抑制效果。
我们的结果表明,通过γ干扰素刺激在体外激活肺癌患者的肺泡巨噬细胞是可能的。这些巨噬细胞获得了针对敏感肿瘤细胞系的抗增殖特性。