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Abstract 10828: Stem-Cell Therapy for Abdominal Aortic Aneurysms in Swine

Authors :
Brian Zilberman
Gaby Ghobrial
Robert Emery
Nicholas De Leo
Clara Zhu
Rebecca Platoff
Ping Zhang
Olga Ostrovsky
Krystal Hunter
Vaishali Krishnadoss
Noshadi Iman
Spencer Brown
Jeffrey P Carpenter
Source :
Circulation. 144
Publication Year :
2021
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2021.

Abstract

Introduction: The current treatment paradigm of abdominal aortic aneurysms (AAA) focuses on observing patients until their disease reaches certain thresholds for intervention, with no preceding treatment available. There is an opportunity to develop drug or cell-based therapies to prevent further aneurysmal growth and decrease the risk of a highly morbid rupture. A previously validated acute AAA swine model was treated directly with gelfoam containing human adipose-derived stem cells (h-ADSCs). Methods: Male Yorkshire swine (n=16) received periadventitial injections (type 1 collagenase and porcine pancreatic elastase) into a 4 cm segment of infrarenal aorta. Experimental group (n=7) received gel foam soaked with 10 million h-ADSCs and control group (n=9) media-soaked gel foam. Aortic diameters (AD) were monitored at post-operative day (POD) 7 and 14 using ultrasound with euthanasia on POD 21. Suprarenal (control) and infrarenal aortas (experimental) were harvested for PCR, mechanical tensiometry testing, histopathological analyses as well as immunohistochemistry (IHC). Each animal served as their own control. Groups were compared with paired t-tests and Mann Whitney U tests. Results: Twelve animals survived until POD 21. Stem cell treated AAAs, unlike controls, demonstrated no growth (-1.6 ± 8.8% vs. 34.8 ± 13.7%, p Conclusion: Stem cell therapy prevents the development of aortic aneurysms in a swine model. Stem cell treated swine with induced AAAs show more normal gross features, histologic, and biochemical properties compared to untreated controls with induced AAAs. Further investigation is merited as a possible translatable therapy for aneurysmal disease.

Details

ISSN :
15244539 and 00097322
Volume :
144
Database :
OpenAIRE
Journal :
Circulation
Accession number :
edsair.doi...........73025b1d5d7f9a1a0063017ae8efd4bb
Full Text :
https://doi.org/10.1161/circ.144.suppl_1.10828