Endotoxin and cytokine removal in sepsis.

C. Tetta, R. Bellomo, P. Inguaggiato, M. Wratten, C. Ronco
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引用次数: 43

Abstract

Sepsis, the leading cause of mortality in intensive care units, is a complex series of interrelated effects caused by the overproduction of multiple mediators and their unrestrained biological activity. Both proinflammatory and antiinflammatory mediators participate in the high complexity of sepsis and explain the failure of specific therapies to improve survival. Continuous extracorporeal therapies have been proposed as therapeutic options and as tools for blood purification in sepsis. Along these lines and in order to achieve higher clearances and mass removal rates, we studied the effects of plasmafiltration coupled with adsorption and provided in vitro and in vivo evidence that adsoprtion of multiple cytokines, activated complement components, and lipid mediators such as the platelet-activating factor occurs. We also showed that such treatment may lead to improved survival in a rabbit model of sepsis and to improved hemodynamics, reduced norepinephrine dose, and restoration of near-to-normal responsiveness of blood leukocytes to endotoxin in humans. It is anticipated that treatment of plasma, as a modular device to conventional hemofiltration, may pave the way to innovative approaches in the extracorporeal treatment of septic patients.
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脓毒症的内毒素和细胞因子去除。
脓毒症是重症监护病房死亡的主要原因,是由多种介质的过量产生及其不受限制的生物活性引起的一系列复杂的相互关联的影响。促炎和抗炎介质都参与了脓毒症的高度复杂性,并解释了特异性治疗无法提高生存率的原因。持续体外治疗已被提出作为治疗选择和血液净化的工具在败血症。沿着这些思路,为了获得更高的清除率和质量去除率,我们研究了血浆过滤与吸附相结合的效果,并提供了体外和体内证据,证明了多种细胞因子、活化补体成分和脂质介质(如血小板活化因子)的吸附发生。我们还表明,这种治疗可以提高兔脓毒症模型的存活率,改善血液动力学,减少去甲肾上腺素剂量,恢复人血液白细胞对内毒素的接近正常的反应性。预计血浆治疗作为传统血液过滤的模块化装置,可能为脓毒症患者体外治疗的创新方法铺平道路。
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Presidential Address: PRESIDENTIAL ADDRESS Fluctuations in the peripheral blood leukocyte and platelet counts in leukocytapheresis in healthy volunteers. Mobilization factors of peripheral blood stem cells in healthy donors. Cytokine removal by plasma exchange with continuous hemodiafiltration in critically ill patients. In vitro evaluation of newly developed adsorbent for selective removal of glycosylated low-density lipoprotein.
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