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用于治疗脓毒症的抗内毒素治疗方案。

Anti-endotoxin therapeutic options for the treatment of sepsis.

作者信息

Lynn W A

机构信息

Cameron Centre, Ealing Hospital, Southall, Middlesex, UK.

出版信息

J Antimicrob Chemother. 1998 Jan;41 Suppl A:71-80. doi: 10.1093/jac/41.suppl_1.71.

Abstract

The identification of lipopolysaccharide binding protein (LBP) and CD14 as key molecules in the cellular response to endotoxin has been a major advance in unravelling the pathophysiological basis of Gram-negative sepsis. Much interest has focused on developing effective anti-endotoxin treatments to abrogate the inflammatory consequences of Gram-negative infection. The therapeutic options can be divided into those aimed at neutralizing or clearing circulating endotoxin, including anti-endotoxin antibodies and endotoxin neutralizing proteins, and those that antagonize the effects of endotoxin on human cells--for example, lipid A analogues. Initial experiences with anti-lipopolysaccharide antibodies have been disappointing but a new generation of anti-endotoxin agents is about to enter clinical trials. Whether these will prove sufficiently effective to reduce the morbidity and mortality of Gram-negative sepsis remains to be seen.

摘要

脂多糖结合蛋白(LBP)和CD14作为细胞对内毒素反应的关键分子被鉴定出来,这是在阐明革兰氏阴性菌败血症病理生理基础方面取得的一项重大进展。人们对开发有效的抗内毒素治疗方法以消除革兰氏阴性菌感染的炎症后果非常感兴趣。治疗选择可分为旨在中和或清除循环内毒素的方法,包括抗内毒素抗体和内毒素中和蛋白,以及拮抗内毒素对人体细胞作用的方法,例如脂多糖A类似物。抗脂多糖抗体的初步试验结果令人失望,但新一代抗内毒素药物即将进入临床试验。这些药物是否能证明足够有效以降低革兰氏阴性菌败血症的发病率和死亡率,还有待观察。

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