Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4839
Title: Interleukin-10 gene transfection of donor pancreas grafts protects against rejection after heterotopic pancreas transplantation in a rat model
Authors: Özden, H.
Kabay, Burhan.
Guven, G.
Acikalin, M.F.
Erbiş, Halil.
Alatas, O.
Keywords: Gene therapy
Interleukin-10
Pancreas transplantation
cytokine
green fluorescent protein
interleukin 10
sodium chloride
streptozocin
virus vector
animal experiment
animal model
animal tissue
article
correlation analysis
diabetes mellitus
gene therapy
genetic transfection
glucose blood level
graft rejection
heterotrophy
histology
histopathology
insulin blood level
male
nonhuman
organ donor
pancreas transplantation
priority journal
rat
rat strain
Animals
Blood Glucose
Diabetes Mellitus, Experimental
Gene Therapy
Graft Rejection
Green Fluorescent Proteins
Humans
Insulin
Male
Pancreas
Pancreas Transplantation
Random Allocation
Rats
Rats, Sprague-Dawley
Rats, Wistar
Transfection
Transplantation, Heterotopic
Abstract: Objective: The aim of this study was to assess the effect of immunoregulatory cytokine interleukin-10 (IL-10) gene therapy on pancreas tissue rejection in a heterotopic pancreas transplantation model. Background: Modulation of inflammatory responses by anti-inflammatory cytokines (e.g., IL-10) has been suggested to minimize organ rejection. In this context, modulation of cytokines using gene therapy could be a new therapeutic modality in preventing organ rejection. Methods: The study was performed using male inbred Wistar rats as recipients and Sprague-Dawley rats as donors. 24 h before transplantation, groups of rats, named IL-10 (n = 20) and green fluorescent protein (GFP, n = 20), were injected with viral vectors Ad5CMVhIL10 or Ad5CMVGFP. Sham-operated rats (n = 20) underwent saline injection only before transplantation. The pancreatic tissue from each of these donor rats was subsequently transplanted into the corresponding groups of streptozotocin- induced diabetic recipient rats. Recipients were thus transfected with either IL-10 (n = 20), GFP-only carrying viral vectors (n = 20) or no viral vectors (normal saline, n = 20). A selected number of animals from each recipient group (n = 5) was sacrificed at weekly intervals for 3 weeks and some were further followed up to 12 weeks before sacrifice. Histological assessment of the pancreatic tissue was made based on rejection and GFP expression. Blood glucose levels were checked daily in all groups until sacrifice. Upon sacrifice, serum cytokine and insulin levels were measured. Histopathological correlations between blood glucose levels, serum insulin levels and serum IL-10 levels were made. Results: IL-10 gene therapy significantly attenuated pancreas rejection compared to controls, provided more normal blood glucose levels and elevated plasma insulin levels. Upon assumed natural deactivation of transferred viruses after 4 weeks, differences between groups in terms of rejection, blood glucose and insulin levels disappeared. Conclusion: These findings suggest that IL-10 gene therapy significantly reduced pancreas rejection. Copyright © 2005 S. Karger AG.
URI: https://hdl.handle.net/11499/4839
https://doi.org/10.1159/000087867
ISSN: 0014-312X
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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