Lonnemann G, Behme T C, Lenzner B, Floege J, Schulze M, Colton C K, Koch K M, Shaldon S
Department of Nephrology, Medizinische Hochschule Hannover, Germany.
Kidney Int. 1992 Jul;42(1):61-8. doi: 10.1038/ki.1992.261.
Pro-inflammatory cytokine-inducing substances derived from cultured E. coli have previously been shown to pass across low-flux regenerated cellulosic dialyzer membranes. In the present study, a sterile filtrate of Pseudomonas maltophilia grown from standard bicarbonate dialysis fluid was used to test the permeability of various dialyzer membranes (regenerated cellulose, cellulose triacetate, polyacrylonitrile, polysulfone and polyamide) to TNF alpha-inducing bacterial substances. Pyrogen-free tissue culture medium (MEM) was recirculated for 60 minutes in the dialysate compartment of a closed-loop dialysis system, then P. maltophilia filtrate was added and recirculation was continued for a further hour. Samples from the dialysate (MEM) and the blood side (containing 10% human plasma in MEM) were incubated with donor mononuclear cells (MNC) for 18 hours and TNF alpha release was measured in MNC supernatants by radioimmunoassay. Five minutes after the addition of P. maltophilia filtrate, mean TNF alpha-inducing activity in the dialysate increased from (mean +/- SEM) 0.10 +/- 0.02 to 18.2 +2- 1.5 (ng/2.5 x 10(6) MNC/18 hr). TNF alpha-inducing activity in the blood side increased with regenerated cellulose from 0.10 +/- 0.01 to 4.57 +/- 1.55 (N = 8; P less than 0.001); with cellulose triacetate from 0.20 +/- 0.05 to 0.44 +/- 0.10 (N = 5; P less than 0.05), and with polyacrylonitrile from 0.10 +/- 0.02 to 1.16 +/- 0.45 (N = 5; P less than 0.03). No increased TNF alpha-inducing activity was observed in the blood side of polysulfone (N = 5) or polyamide dialyzers (N = 5).(ABSTRACT TRUNCATED AT 250 WORDS)
先前已表明,培养的大肠杆菌产生的促炎细胞因子诱导物质能够穿过低通量的再生纤维素透析器膜。在本研究中,用从标准碳酸氢盐透析液中培养出的嗜麦芽窄食单胞菌的无菌滤液来测试各种透析器膜(再生纤维素、三醋酸纤维素、聚丙烯腈、聚砜和聚酰胺)对肿瘤坏死因子α诱导性细菌物质的通透性。无热原的组织培养基(MEM)在闭环透析系统的透析液隔室中循环60分钟,然后加入嗜麦芽窄食单胞菌滤液并继续循环1小时。将透析液(MEM)和血侧(含有10%人血浆的MEM)的样品与供体单核细胞(MNC)孵育18小时,并通过放射免疫测定法测量MNC上清液中的肿瘤坏死因子α释放量。加入嗜麦芽窄食单胞菌滤液5分钟后,透析液中肿瘤坏死因子α的平均诱导活性从(均值±标准误)0.10±0.02增加到18.2±1.5(纳克/2.5×10⁶个MNC/18小时)。血侧的肿瘤坏死因子α诱导活性随着再生纤维素从0.10±0.01增加到4.57±1.55(N = 8;P<0.001);随着三醋酸纤维素从0.20±0.05增加到0.44±0.10(N = 5;P<0.05),随着聚丙烯腈从0.10±0.02增加到1.16±0.45(N = 5;P<0.03)。在聚砜(N = 5)或聚酰胺透析器的血侧未观察到肿瘤坏死因子α诱导活性增加。(摘要截断于250字)