Surficial nano-deposition locoregionally yielding bactericidal super CAR-macrophages expedites periprosthetic osseointegration.
Ziyang LiShengchang ZhangZhipeng FuYing LiuZhentao ManChongdeng ShiChunwei TangChen ChenQihao ChaiZhenmei YangJing ZhangXiaotian ZhaoHailun XuChunwei TangYan WangZiyang LiaoGongchang YuBin ShiKun ZhaoWei LiXinyi JiangPublished in: Science advances (2023)
Tracking and eradicating Staphylococcus aureus in the periprosthetic microenvironment are critical for preventing periprosthetic joint infection (PJI), yet effective strategies remain elusive. Here, we report an implant nanoparticle coating that locoregionally yields bactericidal super chimeric antigen receptor macrophages (CAR-MΦs) to prevent PJI. We demonstrate that the plasmid-laden nanoparticle from the coating can introduce S. aureus -targeted CAR genes and caspase-11 short hairpin RNA (CASP11 shRNA) into macrophage nuclei to generate super CAR-MΦs in mouse models. CASP11 shRNA allowed mitochondria to be recruited around phagosomes containing phagocytosed bacteria to deliver mitochondria-generated bactericidal reactive oxygen species. These super CAR-MΦs targeted and eradicated S. aureus and conferred robust bactericidal immunologic activity at the bone-implant interface. Furthermore, the coating biodegradability precisely matched the bone regeneration process, achieving satisfactory osteogenesis. Overall, our work establishes a locoregional treatment strategy for priming macrophage-specific bactericidal immunity with broad application in patients suffering from multidrug-resistant bacterial infection.
Keyphrases
- bone regeneration
- reactive oxygen species
- multidrug resistant
- staphylococcus aureus
- end stage renal disease
- cell death
- ejection fraction
- stem cells
- total hip arthroplasty
- escherichia coli
- soft tissue
- adipose tissue
- peritoneal dialysis
- newly diagnosed
- chronic kidney disease
- gene expression
- cancer therapy
- klebsiella pneumoniae
- prognostic factors
- genome wide
- bone mineral density
- transcription factor
- oxidative stress
- patient reported outcomes
- combination therapy
- induced apoptosis
- cystic fibrosis
- genome wide analysis