肺炎克雷伯菌
材料科学
微生物学
药品
生物
纳米技术
大肠杆菌
基因
药理学
生物化学
作者
Weiran Li,Ying Hu,Qishu Zhang,Liangqun Hua,Zhongqian Yang,Zhaoling Ren,Xiao Zheng,Weiwei Huang,Yanbing Ma
标识
DOI:10.1021/acsami.1c06701
摘要
Drug resistance of Klebsiella pneumoniae severely threatens human health. Overcoming the mechanisms of K. pneumoniae resistance to develop novel vaccines against drug-resistant K. pneumoniae is highly desired. Here, we report a technology platform that uses high pressure to drive drug-resistant K. pneumoniae to pass through a gap, inducing the formation of stable artificial bacterial biomimetic vesicles (BBVs). These BBVs had little to no bacterial intracellular protein or nucleic acid and had high yields. BBVs were efficiently taken up by dendritic cells to stimulate their maturation. BBVs as K. pneumoniae vaccines had the dual functions of inducing bacteria-specific humoral and cellular immune responses to increase animals' survival rate and reduce pulmonary inflammation and bacterial loads. We believe that BBVs are new-generation technology for bacterial vesicle preparation. Establishment of this BBV vaccine platform can maximally expand preparation technology for vaccines against drug-resistant K. pneumoniae.
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