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内源性致热原能否透过人工膜?

Transfer of endogenous pyrogens across artificial membranes?

作者信息

Lonnemann G, Linnenweber S, Burg M, Koch K M

机构信息

Department of Nephrology, Medizinische Hochschule Hannover, Germany.

出版信息

Kidney Int Suppl. 1998 May;66:S43-6.

PMID:9573572
Abstract

Synthetic high-flux dialyzer membranes used in continuous veno-venous hemofiltration are permeable to middle molecular size endogenous pyrogens, the pro-inflammatory cytokines IL-1 beta and TNF-alpha. The quantities removed by sieving are, however, negligible in vitro as well as in vivo. Adsorption of cytokines to the membrane polymer is the major mechanism of pyrogen removal. Adsorption seems to be semispecific for pro-inflammatory cytokines because levels of anti-inflammatory mediators were not changed or even increased during CVVH. Thus, CVVH may change cytokine profiles in septic patients supporting the predominance of anti-inflammatory over pro-inflammatory activity in plasma. It remains to be demonstrated whether modifications of extracorporeal blood purification systems (high-volume CVVH, plasma separation + adsorption) are able to amplify the change in cytokine profiles and whether this change influences outcome of septic patients.

摘要

用于连续性静脉-静脉血液滤过的合成高通量透析器膜可透过中等分子大小的内源性致热原,即促炎细胞因子白细胞介素-1β和肿瘤坏死因子-α。然而,通过筛滤去除的量在体外和体内均可忽略不计。细胞因子吸附到膜聚合物上是去除热原的主要机制。吸附似乎对促炎细胞因子具有半特异性,因为在连续性静脉-静脉血液滤过期间抗炎介质水平未发生变化甚至升高。因此,连续性静脉-静脉血液滤过可能会改变脓毒症患者的细胞因子谱,支持血浆中抗炎活性优于促炎活性。体外血液净化系统的改良(高容量连续性静脉-静脉血液滤过、血浆分离+吸附)是否能够放大细胞因子谱的变化以及这种变化是否会影响脓毒症患者的预后仍有待证实。

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