“…However, the results from 5-year follow-up demonstrated that approximately 80% of recipient patients had C-peptide present posttransplant, but only 10% maintained insulin independence (4,5). The fact that it requires only 1000 IEQ/kg in human autotransplants compared with 10,000 IEQ/kg in allotransplants reveals that alloreactive T cells contribute the most to islet allograft failure (19). The current paradigm of immunosuppression, including sirolimus and tacrolimus, has nearubiquitous targets of distribution and as a result leads to a number of side effects for the islet recipients and for the implanted islet  cells (20 -25).…”
Local expression of B7-H4 prolongs islet allograft survival in vivo, suggesting translational potential for beta-cell replacement with reduced immune injury.
“…However, the results from 5-year follow-up demonstrated that approximately 80% of recipient patients had C-peptide present posttransplant, but only 10% maintained insulin independence (4,5). The fact that it requires only 1000 IEQ/kg in human autotransplants compared with 10,000 IEQ/kg in allotransplants reveals that alloreactive T cells contribute the most to islet allograft failure (19). The current paradigm of immunosuppression, including sirolimus and tacrolimus, has nearubiquitous targets of distribution and as a result leads to a number of side effects for the islet recipients and for the implanted islet  cells (20 -25).…”
Local expression of B7-H4 prolongs islet allograft survival in vivo, suggesting translational potential for beta-cell replacement with reduced immune injury.
“…Table shows the minimal islet mass expressed as IEQ/kg that has been associated with insulin independence of the recipient in three settings: clinical autologous and allogeneic islet transplantation and pre‐clinical (pig to non‐human primate) islet xenotransplantation . The gap in immunological compatibility remains the main cause for the need of higher number of islets; however, metabolic differences between animal species (such as pigs and Cynomolgous monkeys) further contribute to increased islet mass demand.…”
Section: Human Donor Shortage: the Rationale For Beta‐cell Surrogatesmentioning
confidence: 99%
“…One of the consequences of improving compatibility between donor and recipient will translate to lower islet mass required to achieve glucose control after transplantation. Table 1 shows the minimal islet mass expressed as IEQ/kg that has been associated with insulin independence of the recipient in three settings: clinical autologous and allogeneic islet transplantation and pre-clinical (pig to non-human primate) islet xenotransplantation (13,15,26,32,37,52,53). The gap in immunological compatibility remains the main cause for the need of higher number of islets; however, Fig.…”
Section: Human Donor Shortage: the Rationale For Beta-cell Surrogatesmentioning
Beta-cell replacement is the only physiologically relevant alternative to insulin injections in patients with type 1 diabetes (T1D). Pancreas and islet transplantation from deceased organ donors can provide a new beta-cell pool to produce insulin, help blood glucose management, and delay secondary diabetes complications. For children and adolescents with T1D, whole pancreas transplantation is not a viable option because of surgical complications, whereas islet transplantation, even if it is procedurally simpler, must still overcome the burden of immunosuppression to become a routine therapy for children in the future.
“…In a case study by Illouz et al, a patient suffering from chronic pancreatitis for more than two years and abnormal glucose tolerance test underwent pancreatectomy and islet autotransplantation and remains insulin independent 5 years after transplantation with less than 1,000 IEQ/kg body weight [ 294 ]. Interestingly, the same group has shown that no significant correlation exists between the number of islets transplanted and insulin independence.…”
Section: Autotransplantation For Chronic Pancreatitismentioning
Diabetes mellitus remains one of the leading causes of morbidity and mortality worldwide. According to the Centers for Disease Control and Prevention, approximately 23.6 million people in the United States are affected. Of these individuals, 5 to 10% have been diagnosed with Type 1 diabetes mellitus (T1DM), an autoimmune disease. Although it often appears in childhood, T1DM may manifest at any age, leading to significant morbidity and decreased quality of life. Since the 1960s, the surgical treatment for diabetes mellitus has evolved to become a viable alternative to insulin administration, beginning with pancreatic transplantation. While islet cell transplantation has emerged as another potential alternative, its role in the treatment of T1DM remains to be solidified as research continues to establish it as a truly viable alternative for achieving insulin independence. In this paper, the historical evolution, procurement, current status, benefits, risks, and ongoing research of islet cell transplantation are explored.
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