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用于治疗和预防耐甲氧西林肺炎的肺靶向溶葡萄球菌酶微球。

Lung-Targeting Lysostaphin Microspheres for Methicillin-Resistant Pneumonia Treatment and Prevention.

机构信息

Department of Infectious Diseases, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.

Institute of Translational Medicine, Zhejiang University, Hangzhou 310009, China.

出版信息

ACS Nano. 2021 Oct 26;15(10):16625-16641. doi: 10.1021/acsnano.1c06460. Epub 2021 Sep 28.

Abstract

Multifunctional antimicrobial strategies are urgently needed to treat methicillin-resistant (MRSA) caused pneumonia due to its increasing resistance, enhanced virulence, and high pathogenicity. Here, we report that lysostaphin, a bacteriolytic enzyme, encapsulated within poly(lactic--glycolic acid) microspheres (LyIR@MS) specially treats planktonic MRSA bacteria, mature biofilms, and related pneumonia. Optimized LyIR@MS with suitable diameters could deliver a sufficient amount of lysostaphin to the lung without a decrease in survival rate after intravenous injection. Furthermore, the degradable properties of the carrier make it safe for targeted release of lysostaphin to eliminate MRSA, repressing the expression of virulence genes and improving the sensitivity of biofilms to host neutrophils. In the MRSA pneumonia mouse model, treatment or prophylaxis with LyIR@MS significantly improved survival rate and relieved inflammatory injury without introducing adverse events. These findings suggest the clinical translational potential of LyIR@MS for the treatment of MRSA-infected lung diseases.

摘要

由于耐甲氧西林金黄色葡萄球菌(MRSA)的耐药性增强、毒力增强和致病性高,因此迫切需要采用多功能抗菌策略来治疗由其引起的肺炎。在这里,我们报告称,溶菌酶是一种溶菌酶,被包裹在聚乳酸-羟基乙酸微球(LyIR@MS)内,专门用于治疗浮游状态的 MRSA 细菌、成熟的生物膜和相关肺炎。经过优化的具有合适直径的 LyIR@MS 可以在不降低静脉注射后存活率的情况下向肺部输送足够量的溶菌酶。此外,载体的可降解特性使其能够安全地靶向释放溶菌酶以消除 MRSA,抑制毒力基因的表达,并提高生物膜对宿主中性粒细胞的敏感性。在 MRSA 肺炎小鼠模型中,LyIR@MS 的治疗或预防显著提高了生存率并缓解了炎症损伤,而没有引入不良反应。这些发现表明 LyIR@MS 具有治疗 MRSA 感染性肺病的临床转化潜力。

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