Transplanted human pancreatic islets after long-term insulin independence.

Détails

ID Serval
serval:BIB_F2BE3ACEA912
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Transplanted human pancreatic islets after long-term insulin independence.
Périodique
American journal of transplantation
Auteur⸱e⸱s
Muller Y.D., Gupta S., Morel P., Borot S., Bettens F., Truchetet M.E., Villard J., Seebach J.D., Holmberg D., Toso C., Lobrinus J.A., Bosco D., Berney T.
ISSN
1600-6143 (Electronic)
ISSN-L
1600-6135
Statut éditorial
Publié
Date de publication
04/2013
Peer-reviewed
Oui
Volume
13
Numéro
4
Pages
1093-1097
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Long-term insulin independence after islets of Langerhans transplantation is rarely achieved. The aims of this study were to identify the histological and immunological features of islets transplanted in a type 1 diabetic patient who died of a cerebral hemorrhage after >13 years insulin independence. Islets were pooled from two donors with respectively one and five HLA mismatches. Insulin-positive islets were found throughout the right and left liver, and absent in the pancreas. Two- and three-dimensional analysis showed that islets lost their initial rounded and compact morphology, had a mean diameter of 136 μm and were constituted of an unfolded epithelial band of 39.1 μm. Leukocyte phenotyping showed no evidence of a tolerogenic environment in the islet-containing portal spaces. Finally, HLA typing of microdissected islets showed HLA from the best matched donor in all 23 microdissection samples, compared to 1/23 for the least matched donor. This case report demonstrates that allogeneic islets can survive over 13 years while maintaining insulin independence. Allogeneic islets had unique morphologic features and implanted in the liver regardless of their size. Finally, our results suggest that, in this case, rejection had been prevalent over autoimmunity, although this hypothesis warrants further investigation.
Mots-clé
Adult, Autoimmunity, Diabetes Mellitus, Type 1/therapy, Female, HLA Antigens/chemistry, HLA-DRB1 Chains/genetics, Humans, Immune System, Insulin/therapeutic use, Insulin-Secreting Cells/cytology, Islets of Langerhans Transplantation/methods, Kidney Transplantation/methods, Leukocytes/cytology, Liver/pathology, Microscopy, Fluorescence, Pancreas/pathology, Phenotype, Polymerase Chain Reaction, Treatment Outcome
Pubmed
Web of science
Open Access
Oui
Création de la notice
01/11/2023 15:09
Dernière modification de la notice
13/04/2024 7:06
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