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金黄色葡萄球菌5型和8型荚膜多糖的修订结构,新型糖缀合物疫苗的组成成分。

Revised structures for the capsular polysaccharides from Staphylococcus aureus Types 5 and 8, components of novel glycoconjugate vaccines.

作者信息

Jones Christopher

机构信息

Laboratory for Molecular Structure, National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Herts EN6 3QG, UK.

出版信息

Carbohydr Res. 2005 May 2;340(6):1097-106. doi: 10.1016/j.carres.2005.02.001.

Abstract

Glycoconjugate vaccines based on the capsular polysaccharides (CPSs) from Staphylococcus aureus serotypes 5 and 8 conjugated to genetically detoxified recombinant exoprotein A (rEPA) from Pseudomonas aeruginosa have been shown, in Phase 3 clinical trials, to elicit a strong bactericidal immune response in end-stage renal disease patients. Such vaccines have the potential to reduce morbidity and mortality due to methicillin-resistant Staphylococcus aureus (MRSA), a major cause of hospital-acquired infection. The serotype 5 and 8 polysaccharides have been fully characterized by NMR spectroscopy and full structural analyses carried out. Published structures were found incorrect and the revised structures of the repeat units of the two polysaccharides are: [carbohydrate structure: see text]. Resonances indicative of the presence of peptidoglycan were observed in the spectra of both CPSs, consistent with reports that the CPS is covalently linked to peptidoglycan.

摘要

基于金黄色葡萄球菌5型和8型荚膜多糖(CPS)与铜绿假单胞菌经基因解毒的重组外蛋白A(rEPA)偶联的糖缀合物疫苗,在3期临床试验中已显示,可在终末期肾病患者中引发强烈的杀菌免疫反应。此类疫苗有潜力降低耐甲氧西林金黄色葡萄球菌(MRSA)所致的发病率和死亡率,MRSA是医院获得性感染的主要原因。5型和8型多糖已通过核磁共振光谱进行了全面表征,并开展了完整的结构分析。发现已发表的结构有误,两种多糖重复单元的修订结构如下:[碳水化合物结构:见正文]。在两种CPS的光谱中均观察到了表明存在肽聚糖的共振信号,这与CPS与肽聚糖共价连接的报道一致。

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