J. Oberholzer et al., Human islet transplantation - Lessons from 13 autologous and 13 allogeneictransplantations, TRANSPLANT, 69(6), 2000, pp. 1115-1123
Background. A series of 13 islet autotransplantations and 13 islet allotran
splantations performed between 1992 and 1999 at the University Hospital of
Geneva are presented. Factors affecting the outcome are analyzed.
Methods. Islet autotransplantation has been performed in seven patients wit
h chronic pancreatitis and in six patients with benign tumors undergoing ex
tensive pancreatectomy. Islet allografts were performed in C-peptide-negati
ve patients simultaneously or after a kidney or lung transplantation. Each
recipient received islets from one to four donors. Panel-reactive antibodie
s were monitored by microlymphocytotoxicity test.
Results, Eleven of 13 patients who underwent autotransplantation maintained
insulin independence for 6 months to 5 years. Two years after autologous i
slet transplantation, five of nine patients were insulin independent with a
n glycosylated hemoglobin of 5.9%. Three late islet failures occurred in pa
tients with chronic pancreatitis. Islet yield was significantly lower in pa
tients with chronic pancreatitis than in patients with benign tumors (2044
equivalent islet number/gram resected pancreas versus 5184 equivalent islet
number/gram; P=0.037). In islet allotransplantation, no early graft loss w
as found. All 13 patients who underwent allotransplantation had basal C-pep
tide levels above 0.3 nmol/L for 3 months to 5 years. Mean glycosylated hem
oglobin decreased from 9.1% before transplantation to 5.5% at month 3. Insu
lin independence was achieved in two type I diabetic patients. In four of s
ix patients with graft failure, the graft had induced panel-reactive antibo
dies.
Conclusions. In islet autotransplantation, the reduced number of islets tha
t can be isolated from fibrotic pancreata may be the major limiting factor.
In islet allotransplantation, early graft function can now be consistently
achieved. Islet allografts seem to be highly immunogenic, and chronic isle
t failure cannot be prevented consistently by conventional immunosuppressio
n.