金黄色葡萄球菌
抗生素
微生物学
细胞内
毒力
结合
万古霉素
细胞外
病菌
抗体
细胞内寄生虫
生物
细菌
免疫学
生物化学
数学分析
遗传学
数学
基因
作者
Sophie M. Lehar,Thomas H. Pillow,Min Xu,Leanna R. Staben,Kimberly K. Kajihara,Richard Vandlen,Laura DePalatis,Helga Raab,Wouter L. W. Hazenbos,J. Hiroshi Morisaki,Janice Kim,Summer Park,Martine Darwish,Byoung-Chul Lee,Hilda Hernandez,Kelly M. Loyet,Patrick J. Lupardus,Rina Fong,Donghong Yan,Cécile Chalouni
出处
期刊:Nature
[Nature Portfolio]
日期:2015-11-01
卷期号:527 (7578): 323-328
被引量:743
摘要
Staphylococcus aureus is considered to be an extracellular pathogen. However, survival of S. aureus within host cells may provide a reservoir relatively protected from antibiotics, thus enabling long-term colonization of the host and explaining clinical failures and relapses after antibiotic therapy. Here we confirm that intracellular reservoirs of S. aureus in mice comprise a virulent subset of bacteria that can establish infection even in the presence of vancomycin, and we introduce a novel therapeutic that effectively kills intracellular S. aureus. This antibody-antibiotic conjugate consists of an anti-S. aureus antibody conjugated to a highly efficacious antibiotic that is activated only after it is released in the proteolytic environment of the phagolysosome. The antibody-antibiotic conjugate is superior to vancomycin for treatment of bacteraemia and provides direct evidence that intracellular S. aureus represents an important component of invasive infections.
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