AsiaIPEX is a one-stop-shop for players in the IP industry, facilitating IP trade and connection to the IP world. Whether you are a patent owner interested in selling your IP, or a manufacturer looking to buy technologies to upgrade your operation, you will find the portal a useful resource.

Triple Growth Factor Delivery for Acute Coronary Occlusion

Others

Chin A, et al (2006) PDGF-AB-based functional cardioprotection of the aging rat heart. Exp Gerontol. 41(1):63-8.

Edelberg JM, Cai D, Xaymardan M. (2003) Translation of PDGF cardioprotective pathways. Cardiovasc Toxicol. 2003;3(1):27-35.

Jheng J et al (2006) Growth Factor-Mediated Reversal of Senescent Dysfunction of Ischemia-Induced Cardioprotection. Am J Physiol Heart Circ Physiol. 290(2):H525-30.

Xaymardan M et al (2004) Senescent Impairment in Synergistic Cytokine Pathways That Provide Rapid Cardioprotection in the Rat Heart. J. Exp. Med. 199 (6): 797-804

*Abstract

In his research on cardiac disease, Dr. Jay Edelberg, Assistant Professor of Medicine at the Weill Medical College of Cornell University, has been characterizing the communication between cardiac myocytes and microvascular endothelial cells mediated by platelet-derived growth factor-AB (PDGF-AB). During 2002 he made several discoveries about this pathway from animal experiments that have led to inventions to help prevent and heal cardiac dysfunction associated with aging and disease.

 

This invention is a method of reducing damage following coronary occlusion. His earlier results had shown PDGF to be cardioprotective when delivered 24 hours prior to, but not at time of, coronary occlusion. Hypothesizing that administration of downstream proteins could expand the window of opportunity of cardioprotection from myocardial infarction, the Edelberg lab determined the set of proteins that enhance the beneficial actions of PDGF.

 

The investigators developed a mixture of growth factors (PDGF-AB, VEGF and Angiopoietin-2) that - when delivered by intramyocardial injection at the time of coronary occlusion in a rat infarction model - prevented acute myocardial cell death and reduced myocardial injury measured 14 days after the occlusion to about half of that observed with PBS, PDGF alone, or other protein combinations. Please see J. Exp. Med. 2004 for details.

 

Overall, these studies demonstrate that concomitant delivery of PDGF with other downstream products expanded the therapeutic utility of PDGF cardioprotection from myocardial infarction, suggesting that clinical strategies based on this combination may be useful in treating acute coronary syndromes.

 

Please see D-2911 and D-3123 for related technologies.

*Licensing
Dan-Oscar Antsonda429@cornell.edu212-746-1297
Country/Region
USA

For more information, please click Here
Mobile Device