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IL-6 in malignant pleural effusions and its augmentation by intrapleural instillation of IL-2.

机译:恶性胸腔积液中的IL-6及其通过胸膜内滴注IL-2来增强。

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摘要

The levels and activities of endogenous IL-6 in malignant pleural effusions due to lung cancer before and during daily intrapleural instillations of recombinant IL-2 were examined by enzyme immunoassay and bioassay using an IL-6-dependent murine hybridoma cell line MH60.BSF2. Before therapy, malignant pleural effusions contained various levels of IL-6. Daily intrapleural instillation of recombinant IL-2 for treatment of malignant pleurisy resulted in significant augmentation of the levels and activities of IL-6 in the pleural effusions. On fractionation of the pleural effusion by chromatography, one major peak of material with a mol. wt of 24 kD showed IL-6 activity. In contrast, no significant level of tumour necrosis factor-alpha or IL-1 beta was detectable in pleural effusions before or during local IL-2 therapy. These data suggest that IL-2 is an important regulatory factor of secondary IL-6 production.
机译:通过酶免疫测定法和生物测定法,使用依赖于IL-6的鼠类杂交瘤细胞系MH60.BSF2,通过酶免疫法和生物测定法检查了在重组胸腔积液每天进行胸膜内滴注之前和期间由于肺癌引起的恶性胸腔积液中内源性IL-6的水平和活性。治疗前,恶性胸腔积液含有不同水平的IL-6。每天胸膜内滴注重组IL-2以治疗恶性胸膜炎,导致胸腔积液中IL-6的水平和活性显着增加。通过色谱分离胸腔积液时,物质的一个主峰具有摩尔。 24kD的wt显示IL-6活性。相反,在局部IL-2治疗之前或期间,在胸腔积液中未检测到显着水平的肿瘤坏死因子-α或IL-1β。这些数据表明,IL-2是继发性IL-6产生的重要调控因子。

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