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PMSC-NVs are **peptide-functionalized mesenchymal stem cell-derived nanovesicles** engineered to selectively target vascular regions with disturbed blood flow, a characteristic feature of atherosclerosis-prone sites. These nanovesicles are derived from human mesenchymal stem cells (hMSCs) and are functionalized with the peptide GSPREYTSYMPH (PREY) via plasmid modification, improving their ability to home to injured or inflamed endothelium. PMSC-NVs have demonstrated potent **anti-inflammatory** and **pro-endothelial recovery** effects in preclinical (mouse and porcine) models of atherosclerosis, recapitulating the beneficial properties of hMSCs and presenting a novel **theragnostic platform** for atherosclerosis prevention and treatment[1][5]. Mechanistically, PMSC-NVs act through delivery of bioactive molecular cargo (such as proteins, lipids, RNAs) that modulate inflammation and support vascular repair at sites of endothelial dysfunction. The platform is at a preclinical research stage and is not currently approved for use in humans.
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