Suppr超能文献

针对核心脂多糖决定簇的抗体:与异源脂多糖无交叉反应性。

Antibodies to core lipopolysaccharide determinants: absence of cross-reactivity with heterologous lipopolysaccharides.

作者信息

Heumann D, Baumgartner J D, Jacot-Guillarmod H, Glauser M P

机构信息

Department of Internal Medicine, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

出版信息

J Infect Dis. 1991 Apr;163(4):762-8. doi: 10.1093/infdis/163.4.762.

Abstract

Using monoclonal antibodies directed against defined epitopes of endotoxin core, this study demonstrated that the presentation of lipopolysaccharide (LPS) to antibodies is critical for measuring the specific binding of antibodies to LPS structures. False cross-reactive reactions apparently were observed when free core LPS or lipid A were used as antigens in ELISA, whereas coating with complexes of high-density lipoproteins with core LPS increased both the sensitivity and the specificity of the test compared with coating with free core LPS, so that nonspecific binding of antibodies was largely avoided. Using this technique, it was not possible to find broadly cross-reactive core LPS antibodies after immunization of rabbits and humans with rough mutants of gram-negative bacteria. These observations underscore the need for careful evaluation of the potential for cross-reactivity of antisera and of monoclonal antibodies directed against endotoxin core.

摘要

利用针对内毒素核心特定表位的单克隆抗体,本研究表明脂多糖(LPS)与抗体的呈现对于测量抗体与LPS结构的特异性结合至关重要。当在酶联免疫吸附测定(ELISA)中使用游离核心LPS或脂质A作为抗原时,显然会观察到假交叉反应,而用高密度脂蛋白与核心LPS的复合物包被相比用游离核心LPS包被,可提高检测的灵敏度和特异性,从而在很大程度上避免了抗体的非特异性结合。使用该技术,在用革兰氏阴性菌粗糙突变体免疫兔和人后,未能发现具有广泛交叉反应的核心LPS抗体。这些观察结果强调了仔细评估抗血清和针对内毒素核心的单克隆抗体交叉反应可能性的必要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验