Assessment of 18F-FDG-leukocyte imaging to monitor rejection after pancreatic islet transplantation.
Details
Serval ID
serval:BIB_549E3FAF007E
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Assessment of 18F-FDG-leukocyte imaging to monitor rejection after pancreatic islet transplantation.
Journal
Transplantation proceedings
ISSN
0041-1345 (Print)
ISSN-L
0041-1345
Publication state
Published
Issued date
11/2006
Peer-reviewed
Oui
Volume
38
Number
9
Pages
3033-3034
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Abstract
We sought to investigate the feasibility of 18F-FDG-leukocyte imaging to detect islet rejection.
Two thousand Sprague-Dawley (SD, syngeneic group) or Lewis (allogeneic group) islet equivalents were intraportally injected into SD rat recipients. Four and 7 days after transplantation, 10(8) 18F-FDG-labeled splenocytes were injected into the jugular vein. Splenocytes were harvested from naïve or sensitized (12 days after intraportal transplantation of 2000 Lewis IEQ) SD rats. Positron emission tomography (PET) imaging was started 5 minutes after splenocyte infusion and performed hourly for 4 hours.
One hour after splenocyte injection, FDG was mainly detected in the heart and lungs. It was then further distributed to other organs, and from the second hour, the highest tracer concentration was located in the abdomen. Liver FDG uptake was similar between syngeneic, allogeneic, and sensitized allogeneic groups at 4 and 7 days after islet transplantation.
No islet rejection was detected by 18F-FDG-leukocyte imaging. The amount of transplanted tissue was only few millilitres and the additional related inflammation in case of rejection is small and difficult to detect. The liver showed a relatively high spontaneous tracer uptake; the related background prevented detection of a potential increase in tracer uptake in cases of islet rejection.
Two thousand Sprague-Dawley (SD, syngeneic group) or Lewis (allogeneic group) islet equivalents were intraportally injected into SD rat recipients. Four and 7 days after transplantation, 10(8) 18F-FDG-labeled splenocytes were injected into the jugular vein. Splenocytes were harvested from naïve or sensitized (12 days after intraportal transplantation of 2000 Lewis IEQ) SD rats. Positron emission tomography (PET) imaging was started 5 minutes after splenocyte infusion and performed hourly for 4 hours.
One hour after splenocyte injection, FDG was mainly detected in the heart and lungs. It was then further distributed to other organs, and from the second hour, the highest tracer concentration was located in the abdomen. Liver FDG uptake was similar between syngeneic, allogeneic, and sensitized allogeneic groups at 4 and 7 days after islet transplantation.
No islet rejection was detected by 18F-FDG-leukocyte imaging. The amount of transplanted tissue was only few millilitres and the additional related inflammation in case of rejection is small and difficult to detect. The liver showed a relatively high spontaneous tracer uptake; the related background prevented detection of a potential increase in tracer uptake in cases of islet rejection.
Keywords
Animals, Fluorodeoxyglucose F18, Graft Rejection/diagnostic imaging, Islets of Langerhans Transplantation/immunology, Liver/diagnostic imaging, Positron-Emission Tomography, Radiopharmaceuticals, Rats, Rats, Inbred Lew, Rats, Sprague-Dawley, Transplantation, Homologous, Transplantation, Isogeneic
Pubmed
Web of science
Create date
14/06/2021 8:59
Last modification date
24/05/2024 11:34
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