病菌
细胞内
细胞内寄生虫
细胞
生物
微生物学
免疫学
病毒学
细胞生物学
生物化学
作者
Min Ge,Zesong Ruan,Ya‐Xuan Zhu,W.Z. Wu,Chuang Yang,Han Lin,Jianlin Shi
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-10-30
卷期号:10 (44)
标识
DOI:10.1126/sciadv.adp3976
摘要
In the competition between the pathogen infection and the host defense, infectious microorganisms may enter the host cells by evading host defense mechanisms and use the intracellular biomolecules as replication nutrient. Among them, intracellular Staphylococcus aureus relies on the host cells to protect itself from the attacks by antibiotics or immune system to achieve long-term colonization in the host, and the consequent clinical therapeutic failures and relapses after antibiotic treatment. Here, we demonstrate that intracellular S. aureus surviving well even in the presence of vancomycin can be effectively eliminated using an emerging cell-mimicking therapeutic strategy. These cell mimics with natural killer cell–like activity (NKMs) are composed of a redox-responsive degradable carrier, and perforin and granzyme B within the carrier. NKMs perform far more effectivly than clinical antibiotics in treating intracellular bacterial infections, providing a direct evidence of the NK cell–mimicking immune mechanism in the treatment of intracellular S. aureus .
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