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Diabetes Publish Ahead of Print published online ahead of print December 7, 2007
DOI: 10.2337/db07-0720a

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Original Research

Reduced Immunogenicety of First Trimester Human Fetal Pancreas

Kerstin Brands1, Emily Colvin1, Lindy J Williams1, Rennian Wang2, Richard B Lock3, and Bernard E Tuch1

1Diabetes Transplant Unit, The Prince of Wales Hospital and The University of New South Wales, Sydney, Australia
2Departments of Physiology & Pharmacology and Medicine, University of Western Ontario, London, Canada
3Leukaemia Biology Program, Children's Cancer Institute Australia for Medical Research, University of New South Wales, Sydney, Australia

Objective: The use of human fetal pancreatic tissue may provide a potential source of transplantable β-cells as a therapy for type 1 diabetes. Human fetal pancreas has a remarkable capacity to grow and differentiate in vivo and has been shown to reverse diabetes in rodents. However it is known that human fetal pancreas obtained from the 2nd trimester of gestation is immunogenic and is rejected after transplantation. Tissue obtained from earlier stages might prove to be immune privileged, as has been shown for other tissues.

Research Design and Methods: In this study we determined the immunogenicity of human fetal pancreatic tissue obtained from the 1st trimester of gestation in a humanized mouse model. A microarray study of immunoregulatory gene expression in 1st and 2nd trimester human fetal pancreas was also undertaken.

Results: The analysis of transplanted human fetal pancreata revealed a significantly decreased immunogenicity of the 1st trimester tissue. The 1st trimester grafts showed only limited cellular infiltration and contained numerous insulin positive cells, whereas 2nd trimester tissue was completely infiltrated and rejected. Furthermore an analysis of immunoregulatory genes expressed in 1st and 2nd trimester human fetal pancreas by microarray demonstrated the upregulation of several key immunoregulatory genes in the 2nd trimester tissue. This might account for the reduced immunogenicity of the younger tissue.

Conclusions: Our results provide the first indication that the use of 1st trimester human fetal pancreas for transplantation might increase the survival of the grafts and might decrease the requirement for immunosuppressive drugs.


Correspondence: b.tuch{at}unsw.edu.au


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Related Article:

First-Trimester Human Fetal Pancreas Transplantation for Type 1 Diabetes Treatment: An Alternative Approach for Achieving Long-Term Graft Survival?
Georgia Fousteri and Matthias von Herrath
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G. Fousteri and M. von Herrath
First-Trimester Human Fetal Pancreas Transplantation for Type 1 Diabetes Treatment: An Alternative Approach for Achieving Long-Term Graft Survival?
Diabetes, March 1, 2008; 57(3): 525 - 526.
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