Three-yr follow-up of a type 1 diabetes mellitus patient with an islet xenotransplant


Por: Valdés-González R.A., White D.J.G., Dorantes L.M., Terán L., Garibay-Nieto G.N., Bracho-Blanchet E., Dávila-Pérez R., Evia-Viscarra L., Ormsby C.E., Ayala-Sumuano J.T., Silva-Torres M.L., Ramírez-González B.

Publicada: 1 ene 2007
Categoría: Transplantation

Resumen:
In order to alleviate the shortage of human donors, the use of porcine islets of Langerhans for xenotransplantation in diabetic patients has been proposed as a solution. To overcome rejection, we have developed a procedure for protecting the islets by combining them with Sertoli cells and placing them in a novel subcutaneous device, that generates an autologous collagen covering. A type 1 diabetic woman was closely monitored for 10 months, and then transplanted in two devices with two months of difference and a third time after 22 months. Here we present a three-yr follow-up. The close monitoring induced a rapid decrease in exogenous insulin requirements, which stabilized between 19 and 28 IU/d for nine months. After transplantation, the requirements reduced further to below 6 IU/d and for some weeks she was insulin free. Glycosylated hemoglobin levels decreased concomitantly. Porcine insulin could be detected in the serum after a glucose challenge and insulin positive cells inside a removed device after two yr. No complications have arisen and no porcine endogenous retrovirus infection has been detected through PCR and RT-PCR. This case demonstrates the feasibility of using the xenotransplantation of porcine cells to alleviate metabolic complications and insulin requirements in type 1 diabetic patients. © 2007 Blackwell Munksgaard.

Filiaciones:
Valdés-González R.A.:
 Department of Surgery, Faculty of Medicine, National Autonomous University of Mexico, Mexico City, Mexico

 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

White D.J.G.:
 Robarts Research Institute, University of Western Ontario, London, ON, Canada

Dorantes L.M.:
 Department of Endocrinology, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Terán L.:
 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Garibay-Nieto G.N.:
 Department of Endocrinology, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Bracho-Blanchet E.:
 Department of Surgery, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Dávila-Pérez R.:
 Department of Surgery, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Evia-Viscarra L.:
 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Ormsby C.E.:
 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Ayala-Sumuano J.T.:
 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Silva-Torres M.L.:
 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico

Ramírez-González B.:
 Laboratory of Xenotransplantation, Children's Hospital of Mexico 'Federico Gómez', Calle Dr. Márquez 162, 06720 México City, D.F., Mexico
ISSN: 09020063
Editorial
WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA, Estados Unidos America
Tipo de documento: Article
Volumen: 21 Número: 3
Páginas: 352-357
WOS Id: 000246151700010
ID de PubMed: 17488384

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