Surficial nano-deposition locoregionally yielding bactericidal super CAR-macrophages expedites periprosthetic osseointegration

Author:

Li Ziyang123ORCID,Zhang Shengchang1ORCID,Fu Zhipeng1ORCID,Liu Ying1ORCID,Man Zhentao23,Shi Chongdeng1ORCID,Tang Chunwei1,Chen Chen1ORCID,Chai Qihao2ORCID,Yang Zhenmei1ORCID,Zhang Jing1ORCID,Zhao Xiaotian1ORCID,Xu Hailun3ORCID,Han Maosen1ORCID,Wang Yan1ORCID,Liao Ziyang1,Yu Gongchang4ORCID,Shi Bin4ORCID,Zhao Kun1ORCID,Li Wei23ORCID,Jiang Xinyi1ORCID

Affiliation:

1. NMPA Key Laboratory for Technology Research and Evaluation of Drug Products and Key Laboratory of Chemical Biology (Ministry of Education), Department of Pharmaceutics, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, 44 Cultural West Road, Jinan, Shandong Province 250012, China.

2. Shandong Provincial Hospital, Shandong University, Jinan, Shandong Province 250021, China.

3. Department of Joint Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong Province 250021, China.

4. Neck-Shoulder and Lumbocrural Pain Hospital of Shandong First Medical University, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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