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Longitudinal In Vivo Imaging and Quantification of Human Pancreatic Islet Grafting and Contributing Host Cells in the Anterior Eye Chamber
Published on: June 11, 2020
Graft dysfunction in pancreas and islet transplantation: morphological aspects
Cinthia B Drachenberg1, John C Papadimitriou
1Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA. cdrac001@umaryland.edu
Current Opinion in Organ Transplantation
|December 24, 2010
Summary
Whole pancreas transplantation (WPnTx) and islet transplantation aim for insulin independence in diabetics. This review covers antibody-mediated rejection and posttransplant diabetes mellitus (PTDM) in WPnTx, alongside islet transplant pathology.
Area of Science:
- Transplantation immunology
- Endocrinology
- Pathology
Background:
- β-Cell replacement therapies, including whole pancreas transplantation (WPnTx) and islet transplantation, seek to achieve long-term insulin independence for diabetic patients.
- Despite advances, challenges remain in minimizing side-effects and complications associated with these interventions.
Purpose of the Study:
- To review the current understanding of morphological features of antibody-mediated rejection in WPnTx.
- To summarize the clinical and morphological aspects of posttransplant diabetes mellitus (PTDM), including recurrent autoimmune diabetes mellitus.
- To briefly discuss histopathological data related to islet transplantation.
Main Methods:
- Review of recent literature on histopathology and diagnostic modalities in solid organ transplantation, specifically WPnTx.
- Focus on morphological features of allograft rejection, particularly antibody-mediated rejection.
- Analysis of data concerning the incidence and mechanisms of PTDM.
Main Results:
- Standardization efforts in WPnTx have led to categorization of morphological features of allograft rejection.
- Antibody-mediated rejection is a significant factor impacting both short and long-term graft survival in WPnTx.
- Posttransplant diabetes mellitus (PTDM) occurs with high incidence following WPnTx, necessitating further understanding of its mechanisms.
Conclusions:
- Understanding the morphological characteristics of antibody-mediated rejection and PTDM is crucial for improving WPnTx outcomes.
- Further research into PTDM mechanisms is essential for developing preventive and therapeutic strategies.
- Histopathological insights into islet transplantation are also being considered in the context of β-cell replacement.
