Bioengineered Neutrophil Extinguisher Targets Cascade Immune Pathways of Macrophages for Alleviating Cytokine Storm in Pneumonia.
Anwei ZhouKerong ChenYa GaoXinyuan ZhouZihan TianWeiwei ChenYurui XuZhuo ChenXing-Hai NingPublished in: ACS nano (2023)
Cytokine storm is a common complication of COVID-19 pneumonia and has been proven to contribute to high mortality rates. However, current treatment approaches exhibit limited potential to balance immune response and overproduction of inflammatory cytokines, leading to poor therapeutic outcomes. Herein, a smart bioengineered neutrophil, Extinguisher, composed of live neutrophils encapsulating the liposome formulation of NF-κB suppressor MLN4924 and STING inhibitor H-151 (Lip@MH), is developed for alleviating the hyperinflammatory cytokine storm. Extinguisher inherits motility and chemotaxis characteristics of neutrophils, allowing for the specific delivery and sustained release of Lip@MH within inflamed tissues. Subsequently, Lip@MH effectively transports anti-inflammatory agents into macrophages and synergistically inhibits inflammatory pathways of NF-κB and STING, leading to decreased production of cytokines. In vivo studies demonstrate that Extinguisher not only selectively accumulates at the site of pneumonia caused by Pseudomonas aeruginosa -induced acute lung injury but inhibits the production of inflammatory factors through regulating NF-κB/STING signaling pathways, thereby effectively calming cytokine storm. Importantly, Extinguisher significantly improves therapeutic benefits and survival in mice with acute pneumonia. Therefore, Extinguisher represents an appropriate combination of cell therapy and immunoregulation for cytokine storm intervention and may bring insights into the treatment of COVID-19 pneumonia.
Keyphrases
- signaling pathway
- respiratory failure
- lps induced
- cell therapy
- oxidative stress
- coronavirus disease
- immune response
- pi k akt
- sars cov
- pseudomonas aeruginosa
- anti inflammatory
- randomized controlled trial
- community acquired pneumonia
- gene expression
- liver failure
- stem cells
- mesenchymal stem cells
- cystic fibrosis
- biofilm formation
- combination therapy
- risk assessment
- extracorporeal membrane oxygenation
- risk factors
- drug delivery
- hepatitis b virus
- cell proliferation
- cardiovascular events
- diabetic rats
- weight loss
- dendritic cells
- high glucose
- bone marrow
- acute respiratory distress syndrome
- endothelial cells
- multidrug resistant
- climate change
- replacement therapy
- respiratory syndrome coronavirus
- intensive care unit