Objective of the proposed Islet Cell Resource (ICR) is to continue and further expand the mission of the existing cGMP Islet Cell processing at the University of Miami-Diabetes Research Institute by participating in the proposed network of ICRs. The proposed UM-DRI ICR, together with other selected ICRs, will be responsible for optimization of the procurement of human pancreata from cadaver donors, isolation and quality control of islet cell preparations, distribution of islets for provided applied research or clinical protocols. The proposed ICR will also continue to perform research and development to improve isolation techniques, optimize cellular viability and function, and to improve shipping of human islet cells between centers for research and clinical transplant applications. The proposed UM-DRI ICR has been already working in compliance with the Food and Drug Administration (FDA) Good Manufacturing Practice (GMP) guidelines relevant to Phase cell therapy trials. The objectives of the proposed ICR are to: 1. Optimize the isolation procedures to obtain high yields of functional islet cells. 2. Provide well-characterized islet cells for transplantation into patients with type 1 diabetes. 3. Distribute islet cells to investigators for clinical research or for applied research applications that are in line with the objectives of this RFA. 4. Develop isolation, preservation and shipment procedures that result in maximal islet cell function upon transplantation.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Animal (Mammalian and Nonmammalian) Model, and Animal and Biological Materials Resource Cooperative Agreements (U42)
Project #
1U42RR016603-01
Application #
6440125
Study Section
Special Emphasis Panel (ZRR1-CR-6 (01))
Program Officer
Knazek, Richard
Project Start
2001-09-30
Project End
2006-08-31
Budget Start
2001-09-30
Budget End
2002-08-31
Support Year
1
Fiscal Year
2001
Total Cost
$800,000
Indirect Cost
Name
University of Miami School of Medicine
Department
Surgery
Type
Schools of Medicine
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33146
Vendrame, Francesco; Padilla, Nathalia; Peixoto, Eduardo et al. (2018) Chronic Liraglutide Administration Fails to Suppress Postprandial Glucagon Levels in Type 1 Diabetic Islet Allograft Recipients With Graft Dysfunction. Transplantation 102:e39-e40
Peixoto, Eduardo; Vendrame, Francesco; Arnau, Alvaro et al. (2016) Ten Years of Preserved Kidney Function After Islet Transplant Graft Failure. Diabetes Care 39:e209-e211
Fotino, Carmen; Vergani, Andrea; Fiorina, Paolo et al. (2015) P2X receptors and diabetes. Curr Med Chem 22:891-901
Fotino, Nicoletta; Fotino, Carmen; Pileggi, Antonello (2015) Re-engineering islet cell transplantation. Pharmacol Res 98:76-85
Klein, Dagmar; Álvarez-Cubela, Silvia; Lanzoni, Giacomo et al. (2015) BMP-7 Induces Adult Human Pancreatic Exocrine-to-Endocrine Conversion. Diabetes 64:4123-34
Faleo, Gaetano; Berggren, Per-Olof; Pileggi, Antonello (2014) Intravital imaging of cytotoxic T lymphocytes. Methods Mol Biol 1186:121-9
Cechin, Sirlene; Alvarez-Cubela, Silvia; Giraldo, Jaime A et al. (2014) Influence of in vitro and in vivo oxygen modulation on ? cell differentiation from human embryonic stem cells. Stem Cells Transl Med 3:277-89
Leitão, Cristiane Bauermann; Peixoto, Eduardo Moraes Leao; Westphalen, Antonio C et al. (2014) Liver fat accumulation after islet transplantation and graft survival. Cell Transplant 23:1221-7
Peixoto, Eduardo Moraes Leao; Bozkurt, Nujen Colak; Messinger, Shari et al. (2014) The use of 1.5-anhydroglucitol for monitoring glycemic control in islet transplant recipients. Cell Transplant 23:1213-9
Miki, Atsushi; Ricordi, Camillo; Yamamoto, Toshiyuki et al. (2014) Improved human islet preparations using glucocorticoid and exendin-4. Pancreas 43:1317-22

Showing the most recent 10 out of 107 publications