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高通量透析器内细胞因子诱导物质的保留

Retention of cytokine-inducing substances inside high-flux dialyzers.

作者信息

Lufft V, Mahiout A, Shaldon S, Koch K M, Schindler R

机构信息

Department of Nephrology, Medizinische Hochschule, Hannover, Germany.

出版信息

Blood Purif. 1996;14(1):26-34. doi: 10.1159/000170238.

Abstract

Reprocessing of dialyzers is often performed with nonsterile solutions possibly contaminated with bacterial-derived cytokine-inducing substances. We investigated the retention of cytokine-inducing substances inside the dialyzer during reprocessing in a closed loop in vitro hemodialysis system using a polyamide high flux membrane. After the first in vitro circulation of human whole blood, rinse of the blood compartment (BC) and reverse ultrafiltration (RUF) was performed with either cytokine-inducing substance-free saline or saline contaminated with filtrates from Pseudomonas cultures (6 ng/ml LAL-reactive material); subsequently, dialyzers were stored in 2% formaldehyde. Dialyzers were rinsed with approximately 15 liters pyrogen-free saline before the second circulation using blood from the same donor; the effluates were free of cytokine-inducing substances and formaldehyde. Before and after the blood circulations, peripheral blood mononuclear cells (PBMC) were separated and total production of IL-1 alpha and IL-1 beta was determined after overnight incubation. In noncirculated PBMC as well as in PBMC separated after whole blood circulation with pyrogen-free processed dialyzers, production of IL-1 beta was not detectable. After contaminated rinse of the BC, production of IL-1 beta could be observed (1,600 +/- 1,100 pg/ml, mean +/- SEM). When pyrogen-free RUF was performed after contaminated BC rinse, IL-1 beta production averaged 163 +/- 92 pg/ml when using reused dialyzers, but 1,820 +/- 880 pg/ml when using new dialyzers. After reuse with pyrogen-free BC-rinse and contaminated RUF no IL-1 beta synthesis was observed; however, when pyrogen-free BC-rinse and contaminated RUF was applied to new dialyzers, IL-1 beta synthesis averaged 1,620 +/- 1,200 pg/ml. We conclude that cytokine-inducing substances are retained inside the dialyzer, probably by adsorption to the membrane as well as to the protein layer covering the membrane and are still biologically active after sterilisation. Cytokine-inducing substances adsorbed to the protein layer can be partially removed by RUF. Finally, the protein layer on the membrane appears to reduce the convective transfer of cytokine-inducing substances from the dialysate into the blood compartment.

摘要

透析器的再处理通常使用可能被细菌衍生的细胞因子诱导物质污染的非无菌溶液进行。我们在使用聚酰胺高通量膜的体外闭环血液透析系统中研究了再处理过程中细胞因子诱导物质在透析器内的残留情况。在首次体外循环人全血后,用无细胞因子诱导物质的生理盐水或被铜绿假单胞菌培养滤液污染的生理盐水(6 ng/ml 鲎试剂反应性物质)冲洗血液腔室(BC)并进行反向超滤(RUF);随后,将透析器储存在2%甲醛中。在使用同一供体的血液进行第二次循环之前,用约15升无热原生理盐水冲洗透析器;流出液中无细胞因子诱导物质和甲醛。在血液循环前后,分离外周血单核细胞(PBMC),并在过夜孵育后测定IL-1α和IL-1β的总产生量。在未循环的PBMC以及用无热原处理的透析器进行全血循环后分离的PBMC中,未检测到IL-1β的产生。在对BC进行污染冲洗后,可观察到IL-1β的产生(1600±1100 pg/ml,平均值±标准误)。在对BC进行污染冲洗后进行无热原RUF时,使用复用透析器时IL-1β的产生平均为163±92 pg/ml,而使用新透析器时为1820±880 pg/ml。在用无热原BC冲洗和污染RUF复用后,未观察到IL-1β的合成;然而,当将无热原BC冲洗和污染RUF应用于新透析器时,IL-1β的合成平均为1620±1200 pg/ml。我们得出结论,细胞因子诱导物质保留在透析器内,可能是通过吸附到膜以及覆盖膜的蛋白质层上,并且在灭菌后仍具有生物活性。吸附到蛋白质层上的细胞因子诱导物质可通过RUF部分去除。最后,膜上的蛋白质层似乎减少了细胞因子诱导物质从透析液向血液腔室的对流转移。

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