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小细胞肺癌患者细胞因子分泌的选择性抑制

Selective suppression of cytokine secretion in patients with small-cell lung cancer.

作者信息

Fischer J R, Schindel M, Stein N, Lahm H, Gallati H, Krammer P H, Drings P

机构信息

Thorax-Klinik der LVA Baden, Department of Medical Oncology, Heidelberg-Rohrbach, Germany.

出版信息

Ann Oncol. 1995 Nov;6(9):921-6. doi: 10.1093/oxfordjournals.annonc.a059360.

Abstract

BACKGROUND

Whether or not cytokine secretion is impaired in patients with small-cell lung cancer (SCLC), is unknown. We therefore investigated whether cytokine secretion by immunocompetent cells may be suppressed in patients with SCLC.

PATIENTS AND METHODS

We determined cytokine secretion by lymphocytes and monocytes in whole blood cell cultures from 58 patients with SCLC, 95 patients with non-small-cell lung cancer (NSCLC), 10 patients with nonmalignant lung disease and from 44 normal healthy individuals by using an enzyme-linked immunosorbent assay (ELISA) specific for the different cytokines measured.

RESULTS

Compares to normal controls, immunocompetent cells from patients with SCLC secreted significantly lower amounts of IL-2, IFN alpha, and IFN gamma upon mitogen stimulation. TNF alpha-secretion was significantly reduced in SCLC extensive disease but not in SCLC limited disease. In contrast, secretion of IL-1 alpha and IL-1 beta was not reduced. In patients with NSCLC, secretion of IL-2 and IFN alpha was significantly reduced. Reduction of IFN gamma secretion was significant in metastasized NSCLC and marginally significant in localized NSCLC. Secretion of TNF alpha, IL-1 alpha and IL-1 beta was not impaired. In addition, cytokine secretion in SCLC patients substantially improved upon successful reduction of tumor load by chemotherapy but not upon ineffective chemotherapy. Furthermore, TGF beta 1 suppressed secretion of IL-2, IFN alpha, IFN gamma, TNF alpha but not of IL-1 alpha and IL-1 beta in whole blood cell cultures from healthy individuals.

CONCLUSIONS

Suppression of cytokine secretion in patients with SCLC was selective, dependent on tumor load, different from immunosuppression in NSCLC and seemed to be reconstituted upon reduction of tumor load. These results may suggest interactions between tumor cells and the immune system. TGF beta 1 secreted by SCLC cell lines induced the same selective cytokine suppression as that found in SCLC patients. However, whether or not tumor-derived TGF beta 1 is a factor inducing selective immunosuppression in SCLC patients is presently unclear.

摘要

背景

小细胞肺癌(SCLC)患者的细胞因子分泌是否受损尚不清楚。因此,我们研究了SCLC患者免疫活性细胞的细胞因子分泌是否会受到抑制。

患者与方法

我们通过使用针对所测不同细胞因子的酶联免疫吸附测定(ELISA),测定了58例SCLC患者、95例非小细胞肺癌(NSCLC)患者、10例非恶性肺部疾病患者以及44名正常健康个体全血细胞培养物中淋巴细胞和单核细胞的细胞因子分泌情况。

结果

与正常对照组相比,SCLC患者的免疫活性细胞在有丝分裂原刺激下分泌的IL-2、IFNα和IFNγ量显著降低。SCLC广泛期患者的TNFα分泌显著减少,但局限期患者未减少。相比之下,IL-1α和IL-1β的分泌未减少。NSCLC患者中,IL-2和IFNα的分泌显著减少。转移的NSCLC患者中IFNγ分泌的减少显著,局部NSCLC患者中则略有显著。TNFα、IL-1α和IL-1β的分泌未受损。此外,SCLC患者在通过化疗成功降低肿瘤负荷后,细胞因子分泌有显著改善,但无效化疗后则无改善。此外,TGFβ1抑制健康个体全血细胞培养物中IL-2、IFNα、IFNγ、TNFα的分泌,但不抑制IL-1α和IL-1β的分泌。

结论

SCLC患者的细胞因子分泌抑制具有选择性,取决于肿瘤负荷,不同于NSCLC中的免疫抑制,且在肿瘤负荷降低后似乎可恢复。这些结果可能提示肿瘤细胞与免疫系统之间存在相互作用。SCLC细胞系分泌的TGFβ1诱导了与SCLC患者中相同的选择性细胞因子抑制。然而,肿瘤来源的TGFβ1是否是诱导SCLC患者选择性免疫抑制的一个因素目前尚不清楚。

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