Pancreatic islet allograft in spleen with immunossuppression with cyclosporine. Experimental model in dogs

Author:

Waisberg Jaques1,Neff Charles Benjamin1,Waisberg Daniel Reis2,Germini Demetrius3,Gonçalves José Eduardo,Zanotto Arnaldo4,Speranzini Manlio Basilio1

Affiliation:

1. Faculty of Medicine of ABC, Brazil

2. University of Sao Paulo, Brazil

3. Hospital do Servidor Publico Estadual, Brazil

4. USP, Brazil

Abstract

PURPOSE: To study the functional behavior of the allograft with immunosuppression of pancreatic islets in the spleen. METHODS: Five groups of 10 Mongrel dogs were used: Group A (control) underwent biochemical tests; Group B underwent total pancreatectomy; Group C underwent total pancreatectomy and pancreatic islet autotransplant in the spleen; Group D underwent pancreatic islet allograft in the spleen without immunosuppressive therapy; Group E underwent pancreatic islet allograft in the spleen and immunosuppression with cyclosporine. All of the animals with grafts received pancreatic islets prepared by the mechanical-enzymatic method - stationary collagenase digestion and purification with dextran discontinuous density gradient, implanted in the spleen. RESULTS: The animals with autotransplant and those with allografts with immunosuppression that became normoglycemic showed altered results of intravenous tolerance glucose (p < 0.001) and peripheral and splenic vein plasmatic insulin levels were significantly lower (p < 0.001) in animals that had allografts with immunosuppression than in those with just autotransplants. CONCLUSIONS: In the animals with immunosupression with cyclosporine subjected to allograft of pancreatic islets prepared with the mechanical-enzymatic preparation method (stationary collagenase digestion and purification with dextran discontinuous density gradient), the production of insulin is decreased and the response to intravenous glucose is altered.

Publisher

FapUNIFESP (SciELO)

Subject

Surgery

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3. Two-layer cold storage method for pancreas and islet cell transplantation;Fujino Y;World J Gastroenterol.,2010

4. Hepatic artery vs. portalvein infusion of microbeads;Wang W;Xenotransplantation.,2010

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