Abstract
The initial step in successful islet transplantation is procurement of healthy donor islets. Given the limited number of donor pancreata selected for islet isolation and that islets from multiple donors are typically required to obtain insulin independence, it is critical to improve pancreas procurement rates and yield of islets for transplantation. Islets are delicate microorgans that are susceptible to apoptosis, hypoxia, and ischemia during isolation, culture, and the peritransplant period. Once the islets are engrafted, both prompt revascularization and protection from beta-cell death and graft rejection are key to secure long-term survival and function. To facilitate the engraftment of more robust islets suitable for combating the challenging isolation period and proinflammatory transplantation milieu, numerous approaches have been employed to prevent beta-cell dysfunction and death including immune modulation, prevention of apoptosis and hypoxia, as well as stimulation of growth factors, angiogenesis, and reinnervation. In addition to briefly discussing islet isolation procedures, procurement rates, and islet transplantation, the relevant literature pertaining to successful suboptimal islet transplantation is reviewed to provide insight into potential approaches to balance the limited supply of available donor islets.
Highlights
Islet transplantation is an experimental procedure available to a limited group of type 1 diabetes patients
Longitudinal studies have shown that 75% of islet grafts fail within the first two years after transplantation, and patients return to exogenous insulin therapy [7]
The beta score has been found to be inversely proportional to the level of panel reactivity antibodies such that a high level of panel reactive antibodies is associated with a lower beta score that is indicative of a decreased islet transplantation success rate and vice versa [9]
Summary
Islet transplantation is an experimental procedure available to a limited group of type 1 diabetes patients. It is of importance to the islet transplantation field to optimize the islet isolation protocol as well as minimize the various destabilizing or toxic contributors to the graft environment, since multiple factors reduce the effective number of functional islets after transplantation To this end several recent promising advances have been made to optimize the field: one study persufflated the pancreas to increase oxygenation of the tissue which elevates ATP levels during preservation [27]; another study targeted donor-specific memory T cells with a neutralizing antibody to the adhesion molecule lymphocyte function-associated antigen 1 in combination with a cocktail of basiliximab and sirolimus or belatacept in order to minimize the activity of this blockade-resistant population of memory T cells [28]
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