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New nanotherapy targets inflammation of arteries in cardiovascular diseases

manhattantribune.com by manhattantribune.com
11 October 2024
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New nanotherapy targets inflammation of arteries in cardiovascular diseases
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LR: Plaque levels in an artery before and after nanotherapy infusion. Credit: Natural communications (2024). DOI: 10.1038/s41467-024-52005-1

Inflammation of the arteries is one of the main precursors and drivers of cardiovascular disease, the leading cause of death in the United States. This inflammation is associated with the buildup of dangerous plaque inside the arteries. Advanced treatments are needed to target this inflammation in patients. Researchers at Michigan State University have tested a new infusion of nanotherapeutic nanoparticles that precisely targets inflammation and activates the immune system to help clear arterial plaque.

The research is published in the journal Natural communications.

“There are two different things that people seem to be afraid of when it comes to plaques,” said Bryan Smith, an associate professor in the College of Engineering’s department of biomedical engineering and the Institute of Science and Technology. Quantitative Health Engineering from MSU. “A lot of people don’t really understand the difference between them.”

The first example is when your artery becomes blocked (for example, a 95-99% blockage). Often, symptoms such as chest pain or pressure or nausea and dizziness appear beforehand and doctors place a stent in the artery to increase blood flow. The second is when the plaque is very inflammatory. This can make the plaque vulnerable to rupture, which can lead to blocked arteries elsewhere in the body.

“It’s the scariest problem that leads to most heart attacks,” Smith said. “Because such plaques do not necessarily block a large part of the artery, and because the effects of the rupture can very suddenly completely block blood flow, such a heart attack can seem to come out of nowhere.”

“Large batch” SWNTs retain their expected physicochemical properties and induce phagocytosis in vitro. Physicochemical characterization of SWNTs loaded in large batches of SHP1i shows successful loading and release of SHP1i in acidic solutions. A DLS; b UV-Vis spectroscopy; And c FT-IR spectroscopy of SWNT and SWNT-Cy5.5-SHP1i; d Release of SHP1i from SWNTs at neutral and acidic pH. Data are presented as mean values ​​± SD. n = 3 on independent repetitions; e The in vitro incucyte phagocytosis assay demonstrates that large batch SWNT-SHP1i treatment of RAW264.7 macrophages significantly increases phagocytosis of apoptotic cells compared to SWNT treatment. ****P. < 0.0001 by unpaired two-tailed t test. Data are presented as mean values ​​± SEM. n= 16 per group on technical repetitions. Credit: Natural communications(2024). DOI: 10.1038/s41467-024-52005-1

Smith and his team, including postdoctoral co-authors Yapei Zhang and Manisha Kumari, created nanoparticles (materials finer than a human hair) that they used to develop a nanotherapy infusion. Nanotherapy selectively targets a specific type of immune cell that enters and becomes part of the plaque. These treated cells “eat away” at parts of the plaque core, removing it from the artery wall and decreasing levels of inflammation in the blood vessels.

Previous studies by Smith and colleagues, the Leeper Lab at Stanford University, tested the perfusion in mice and now in porcine models, to prove the efficacy of the perfusion and, more importantly, its lack of harm. side effects due to its precise immune targeting.

“Using PET (positron emission tomography), we were able to measure the effects of the therapy on the pigs’ arteries,” Smith said. “We have shown in animal models such as pigs that we can decrease levels of inflammation in plaque, not only through this PET imaging technique used clinically, but also through molecular testing. Equally important , we did not see any of the side effects that would have been anticipated if the therapy had not been precisely targeted.”

Previous studies in mice required hundreds of microliters of nanotherapy infusion, but more recently, Smith and his team achieved a measurable impact in pigs by increasing the amount produced in liters. These volumes are within the range necessary for human use. This study represents a crucial step toward translating safer and more effective cardiovascular therapies into patient clinical trials.

More information:
Sharika Bamezai et al, Pro-efferocyte nanotherapies reduce vascular inflammation without inducing anemia in a large animal model of atherosclerosis, Natural communications(2024). DOI: 10.1038/s41467-024-52005-1

Provided by Michigan State University

Quote: New nanotherapy targets arterial inflammation in cardiovascular disease (October 10, 2024) retrieved October 10, 2024 from

This document is subject to copyright. Except for fair use for private study or research purposes, no part may be reproduced without written permission. The content is provided for informational purposes only.



Tags: arteriescardiovasculardiseasesinflammationnanotherapytargets
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