首页> 外文期刊>European journal of clinical investigation >Acute-phase response patterns in isolated hepatic perfusion with tumour necrosis factor alpha (TNF-alpha) and melphalan in patients with colorectal liver metastases.
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Acute-phase response patterns in isolated hepatic perfusion with tumour necrosis factor alpha (TNF-alpha) and melphalan in patients with colorectal liver metastases.

机译:大肠肝转移患者的孤立性肝灌注中肿瘤坏死因子α(TNF-alpha)和美法仑的急性期反应模式。

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BACKGROUND: In this study, we have evaluated hepatotoxicity, secondary cytokine production and hepatic acute-phase response (APR) in patients who underwent isolated hepatic perfusion (IHP) with tumour necrosis factor (TNF) alpha and melphalan for irresectable colorectal liver metastases. DESIGN: An extracorporeal veno-venous bypass was used to shunt blood from the lower body and intestines to the heart. Inflow catheters were placed in the hepatic artery and portal vein, and an outflow catheter in the inferior caval vein. The liver was perfused for 60 min with 0.4 mg of TNF-alpha plus 1 mg kg-1 melphalan (IHPTM group, n = 6) or 1 mg kg-1 melphalan (IHPM group, n = 3). The liver was washed with macrodex before restoring vascular continuity. RESULTS: After the washout procedure, a TNF-alpha peak (169 +/- 38 pg mL-1) was demonstrated in the IHPTM group only. Both groups demonstrated peak levels of interleukin 6 (IL-6) in the perfusate as well as systemically. These were significantly higher in the IHPTM group. Acute-phase protein (APP) levels followed a similar pattern as has been demonstrated after major surgery, with no significant differences between both groups. The addition of TNF-alpha to the perfusate did not lead to a significant difference in APP levels and the time course between groups. CONCLUSIONS: IHP with TNF and melphalan is followed by a transient systemic peak of TNF directly after liver washout. Secondary IL-6 induction was seen in the present study after IHP with and without TNF, which was highest when TNF was added. This phenomenon cannot be extrapolated to APP induction, which appeared unaffected by the addition of TNF, presumably because the surgical procedure itself already causes maximal stimulation of APP production.
机译:摘要背景:在这项研究中,我们评估了接受了肿瘤坏死因子(TNF)α和美法仑的独立肝灌注(IHP)治疗无法切除的结直肠肝转移的患者的肝毒性,继发性细胞因子产生和肝急性期反应(APR)。设计:体外静脉-静脉旁路被用来将血液从下半身和肠道分流到心脏。流入导管放置在肝动脉和门静脉中,流出导管放置在下腔静脉中。用0.4 mgTNF-α加1 mg kg-1 melphalan(IHPTM组,n = 6)或1 mg kg-1 melphalan(IHPM组,n = 3)灌注肝脏60分钟。在恢复血管连续性之前,先用Macrodex清洗肝脏。结果:冲洗程序后,仅在IHPTM组中显示出TNF-α峰(169 +/- 38 pg mL-1)。两组均在灌流液和全身液中均显示出白介素6(IL-6)的峰值水平。在IHPTM组中,这些比例明显更高。急性期蛋白(APP)的水平与大手术后的情况相似,两组之间无显着差异。在灌注液中添加TNF-α不会导致APP水平和组间时间进程的显着差异。结论:在肝冲洗后,IHP伴有TNF和美法仑,随后是TNF的短暂系统性峰值。在有和没有TNF的IHP后,在本研究中发现了继发性IL-6诱导,这在添加TNF时最高。这种现象不能外推到APP诱导,这似乎不受TNF的添加的影响,大概是因为外科手术本身已经引起了APP产生的最大刺激。

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