Bielefeldt-Ohmann H, Marzo A L, Himbeck R P, Jarnicki A G, Robinson B W, Fitzpatrick D R
University of Western Australia Department of Medicine, Queen Elizabeth II Medical Centre, Nedlands.
Cancer Immunol Immunother. 1995 Apr;40(4):241-50. doi: 10.1007/BF01519898.
A role for interleukin-6 (IL-6) in malignant mesothelioma has been suggested by the clinically presenting symptoms of mesothelioma patients, which include fever, weight loss and thrombocytosis. A murine model of malignant mesothelioma was therefore used to examine the potential role of IL-6 in this cancer type and whether the effect of interferon alpha (IFN alpha) therapy on mesothelioma might be mediated, in part, by regulating IL-6 levels and/or IL-6-induced pathobiology. A panel of human and murine mesothelioma cell lines was assayed for endogenous IL-6 production in a bioassay, and for IL-6-mRNA expression. Four out of 5 human and 5 out of 15 murine mesothelioma cell lines produced moderate to high levels of bioactive IL-6 in vitro. This result was corroborated by mRNA detection. One of the representative murine cell lines, AB22, was chosen for further in vivo studies in the murine mesothelioma model. In AB22-inoculated mice detectable serum IL-6 levels were found to precede macroscopically detectable tumour growth, clinical signs (cachexia, abdominal distension, diarrhoea) and changes in the peripheral lymphoid organs (cell depletion and functional depression). Treatment with anti-IL-6 antibody curtailed the clinical symptoms (P < 0.001), as did treatment with recombinant human (rhu) IFN alpha (P < 0.001). Neither anti-IL-6 antibody nor rhuIFN alpha had a direct growth-inhibitory effect on the AB22 mesothelioma cell line in vitro, however, in vivo rhuIFN alpha treatment of mice inoculated with AB22 cells attenuated both IL-6 mRNA expression in the tumours and serum IL-6 levels, ameliorated the depression of lymphocyte activities, and enhanced the number of tumour-infiltrating lymphocytes and macrophages. On the basis of these results it is suggested that IL-6 mediates some of these effects, directly or indirectly, and that a combination therapy of rhuIFN alpha and anti-IL-6 antibody may be an improved palliative treatment for patients with malignant mesothelioma.
间皮瘤患者的临床症状(包括发热、体重减轻和血小板增多)提示白细胞介素-6(IL-6)在恶性间皮瘤中发挥作用。因此,利用恶性间皮瘤小鼠模型来研究IL-6在这种癌症类型中的潜在作用,以及α干扰素(IFNα)治疗间皮瘤的效果是否可能部分通过调节IL-6水平和/或IL-6诱导的病理生物学过程来介导。通过生物测定法检测一组人和小鼠间皮瘤细胞系的内源性IL-6产生情况,并检测IL-6 mRNA表达。5个人类间皮瘤细胞系中的4个以及15个小鼠间皮瘤细胞系中的5个在体外产生中度至高水平的生物活性IL-6。mRNA检测证实了这一结果。选择其中一个具有代表性的小鼠细胞系AB22,用于在小鼠间皮瘤模型中进行进一步的体内研究。在接种AB22的小鼠中,可检测到的血清IL-6水平先于肉眼可检测到的肿瘤生长、临床症状(恶病质、腹胀、腹泻)以及外周淋巴器官的变化(细胞耗竭和功能抑制)出现。用抗IL-6抗体治疗可减轻临床症状(P < 0.001),用重组人(rhu)IFNα治疗也有同样效果(P < 0.001)。然而,抗IL-6抗体和rhuIFNα在体外对AB22间皮瘤细胞系均无直接生长抑制作用,但在体内,用rhuIFNα治疗接种AB22细胞的小鼠可减弱肿瘤中IL-6 mRNA表达和血清IL-6水平,改善淋巴细胞活性的抑制,并增加肿瘤浸润淋巴细胞和巨噬细胞的数量。基于这些结果,提示IL-6直接或间接介导了其中一些效应,并且rhuIFNα和抗IL-6抗体联合治疗可能是恶性间皮瘤患者一种更好的姑息治疗方法。