Neutrophil membrane-coated nanoparticles inhibit synovial inflammation and alleviate joint damage in inflammatory arthritis.
Qiangzhe ZhangDiana DehainiYue ZhangJulia ZhouXiangyu ChenLifen ZhangRonnie H FangWeiwei GaoLiangfang ZhangPublished in: Nature nanotechnology (2018)
Rheumatoid arthritis is a common chronic inflammatory disorder and a major cause of disability. Despite the progress made with recent clinical use of anti-cytokine biologics, the response rate of rheumatoid arthritis treatment remains unsatisfactory, owing largely to the complexity of cytokine interactions and the multiplicity of cytokine targets. Here, we show a nanoparticle-based broad-spectrum anti-inflammatory strategy for rheumatoid arthritis management. By fusing neutrophil membrane onto polymeric cores, we prepare neutrophil membrane-coated nanoparticles that inherit the antigenic exterior and associated membrane functions of the source cells, which makes them ideal decoys of neutrophil-targeted biological molecules. It is shown that these nanoparticles can neutralize proinflammatory cytokines, suppress synovial inflammation, target deep into the cartilage matrix, and provide strong chondroprotection against joint damage. In a mouse model of collagen-induced arthritis and a human transgenic mouse model of arthritis, the neutrophil membrane-coated nanoparticles show significant therapeutic efficacy by ameliorating joint damage and suppressing overall arthritis severity.
Keyphrases
- rheumatoid arthritis
- oxidative stress
- mouse model
- disease activity
- induced apoptosis
- interstitial lung disease
- ankylosing spondylitis
- diabetic rats
- anti inflammatory
- endothelial cells
- multiple sclerosis
- drug delivery
- cancer therapy
- signaling pathway
- cell proliferation
- walled carbon nanotubes
- systemic lupus erythematosus
- idiopathic pulmonary fibrosis
- tissue engineering