Critical Care Medicine Department, Clinical Center, National Institutes of Health, Building 10, Room 2C145, Bethesda, MD 20892, USA.
Expert Opin Drug Metab Toxicol. 2011 Apr;7(4):479-94. doi: 10.1517/17425255.2011.558190. Epub 2011 Feb 17.
Sepsis remains a leading cause of death worldwide. Despite years of extensive research, effective drugs that inhibit the pro-inflammatory effects of lipopolysaccharide (LPS) and improve outcome when added to conventional sepsis treatments are lacking. Eritoran tetrasodium (E5564) is a promising candidate therapy for sepsis belonging to a new class of such drugs which inhibit LPS-induced inflammation by blocking toll-like receptor 4.
This review focuses on the rationale for the use of eritoran tetrasodium in sepsis as well as on its pharmacokinetics, pharmacodynamics, efficacy and safety. Preclinical and clinical studies from a MEDLINE/PubMed literature search in August 2010 with the search terms 'eritoran' and 'E5564' are discussed.
Preclinical in vitro and in vivo studies of eritoran tetrasodium indicate it can limit excessive inflammatory mediator release associated with LPS and improve survival in sepsis models. While early clinical results are promising, its efficacy and safety for treating patients with sepsis are currently under investigation. Even if the ongoing Phase III clinical trial enrolling patients with severe sepsis and increased risk of death shows benefit from eritoran, questions remain and confirmatory studies would be necessary to define its clinical usage.
败血症仍然是全球范围内的主要死亡原因。尽管经过多年的广泛研究,缺乏有效的药物来抑制脂多糖(LPS)的促炎作用,并在常规败血症治疗中添加这些药物来改善预后。埃替拉滨四钠盐(E5564)是一种有前途的败血症候选治疗药物,属于通过阻断 Toll 样受体 4 抑制 LPS 诱导的炎症的新型药物。
本综述重点介绍了埃替拉滨四钠盐在败血症中的应用原理,以及其药代动力学、药效学、疗效和安全性。讨论了 2010 年 8 月通过 MEDLINE/PubMed 文献检索使用“eritoran”和“E5564”这两个检索词的相关研究。
埃替拉滨四钠盐的临床前体外和体内研究表明,它可以限制与 LPS 相关的过度炎症介质释放,并改善败血症模型中的存活率。虽然早期的临床结果很有希望,但它在治疗败血症患者方面的疗效和安全性目前正在研究中。即使正在进行的招募严重败血症和死亡风险增加的患者的 III 期临床试验显示埃替拉滨有益,仍存在疑问,需要进行确证性研究来确定其临床应用。