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使用新型以及经甲醛或Renalin处理的纤维素透析器进行体外血液透析期间的细胞因子产生情况。

Cytokine production during in vitro hemodialysis with new and formaldehyde- or renalin-reprocessed cellulose dialyzers.

作者信息

Pereira B J, Snodgrass B, Barber G, Perella C, Chopra S, King A J

机构信息

Division of Nephrology, New England Medical Center, Boston, MA 02111, USA.

出版信息

J Am Soc Nephrol. 1995 Oct;6(4):1304-8. doi: 10.1681/ASN.V641304.

Abstract

Critics of reuse have suggested that patients treated with reprocessed dialyzers are exposed to pyrogen trapped from the water or solutions used during the reprocessing cycle, thereby triggering the synthesis and release of proinflammatory cytokines, resulting in cachexia. To test this hypothesis, the production of interleukin (IL)-1 alpha by peripheral blood mononuclear cells (PBMC) during in vitro dialysis with new or reprocessed cellulose dialyzers was compared. An in vitro closed-loop dialysis circuit was created with standard hemodialysis blood lines and either new cellulose dialyzers or dialyzers reprocessed 10 times with either formaldehyde/bleach (formaldehyde) or peracetic acid/hydrogen peroxide mixture (Renalin). The circuit was rinsed with 2 L or more of pyrogen-free normal saline before the start of in vitro dialysis until the blood compartment tested negative for residual formaldehyde/Renalin. Heparinized whole blood from healthy volunteers was circulated for 3 h in the blood compartment at 100 mL/min at 37 degrees C. The dialysate compartment was sealed. Peripheral blood mononuclear cells (PBMC) were harvested from the blood compartment before and at the end of 3 h of in vitro dialysis. Total IL-1 alpha synthesis (cell associated plus secreted) by unstimulated and endotoxin-stimulated PBMC was measured by a specific, non-cross-reactive radioimmunoassay. After 3 h of in vitro dialysis, IL-1 alpha production (in picograms per 2.5 million PBMC) by unstimulated PBMC increased from 354 +/- 63 at baseline to 454 +/- 57 with new dialyzers (P = 0.25), from 453 +/- 101 to 450 +/- 67 with formaldehyde-reprocessed dialyzers (P = 0.98), and from 360 +/- 61 to 538 +/- 144 with Renalin-reprocessed dialyzers (P = 0.23). IL-1 alpha production by endotoxin-stimulated PBMC increased from 5,214 +/- 996 to 9,237 +/- 929 with new dialyzers (P < = 0.001), from 6,395 +/- 955 to 9,636 +/- 1,058 with formaldehyde-reprocessed dialyzers (P = 0.006), and from 7,561 +/- 1,000 to 10,092 +/- 2,470 with Renalin-reprocessed dialyzers (P = 0.32). However, there were no significant differences among groups with respect to IL-1 alpha production by unstimulated or endotoxin-stimulated PBMC either before or after 3 h of in vitro dialysis. These data argue against the suggestion that exposure to reprocessed dialyzers results in enhanced synthesis of proinflammatory cytokines. In fact, reprocessed dialyzers probably induce less cytokine production than do new cellulose dialyzers.

摘要

复用透析器的批评者认为,使用再处理透析器治疗的患者会接触到再处理过程中从水或溶液中捕获的热原,从而触发促炎细胞因子的合成和释放,导致恶病质。为了验证这一假设,比较了使用新的或再处理的纤维素透析器进行体外透析期间外周血单核细胞(PBMC)白细胞介素(IL)-1α的产生情况。使用标准血液透析血路以及新的纤维素透析器或用甲醛/漂白剂(甲醛)或过氧乙酸/过氧化氢混合物(Renalin)再处理10次的透析器创建了一个体外闭环透析回路。在体外透析开始前,用2L或更多无热原生理盐水冲洗回路,直到血液腔检测到残留甲醛/ Renalin呈阴性。来自健康志愿者的肝素化全血在37℃下以100mL / min的速度在血液腔中循环3小时。透析液腔被密封。在体外透析3小时之前和结束时从血液腔中采集外周血单核细胞(PBMC)。通过特异性、非交叉反应性放射免疫测定法测量未刺激和内毒素刺激的PBMC的总IL-1α合成(细胞相关加分泌)。体外透析3小时后,未刺激的PBMC产生的IL-1α(每250万个PBMC中的皮克数)从基线时的354±63增加到使用新透析器时的454±57(P = 0.25),使用甲醛再处理透析器时从453±101增加到450±67(P = 0.98),使用Renalin再处理透析器时从360±61增加到538±144(P = 0.23)。内毒素刺激的PBMC产生的IL-1α使用新透析器时从5214±996增加到9237±929(P≤0.001),使用甲醛再处理透析器时从6395±955增加到9636±1058(P = 0.006),使用Renalin再处理透析器时从7561±1000增加到10092±2470(P = 0.32)。然而,在体外透析3小时之前或之后,未刺激或内毒素刺激的PBMC产生的IL-1α在组间没有显著差异。这些数据反驳了接触再处理透析器会导致促炎细胞因子合成增加的观点。事实上,再处理透析器可能比新的纤维素透析器诱导产生的细胞因子更少。

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