Improvement in β-Cell Secretory Capacity After Human Islet Transplantation According to the CIT07 Protocol

التفاصيل البيبلوغرافية
العنوان: Improvement in β-Cell Secretory Capacity After Human Islet Transplantation According to the CIT07 Protocol
المؤلفون: Malek Kamoun, Ali Naji, Cornelia Dalton-Bakes, Maral Palangian, Kumar Vivek, Zaw Min, Eline T. Luning Prak, Eileen Markmann, Michael R. Rickels, Chengyang Liu, Clyde F. Barker, Carissa Fuller, Scott A. Soleimanpour, Richard D. Shlansky-Goldberg, Allen J. Chiou
المصدر: Diabetes
بيانات النشر: American Diabetes Association, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Edmonton protocol, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, Islets of Langerhans Transplantation, Urology, 030209 endocrinology & metabolism, 030230 surgery, Tacrolimus, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Insulin-Secreting Cells, Internal medicine, Diabetes mellitus, Insulin Secretion, Internal Medicine, medicine, Humans, Hypoglycemic Agents, Insulin, Original Research, Sirolimus, geography, geography.geographical_feature_category, C-Peptide, C-peptide, business.industry, Immunosuppression, Middle Aged, Islet, medicine.disease, 3. Good health, Transplantation, Diabetes Mellitus, Type 1, Treatment Outcome, Endocrinology, chemistry, Female, Immunology and Transplantation, business, Immunosuppressive Agents, medicine.drug
الوصف: The Clinical Islet Transplantation 07 (CIT07) protocol uses antithymocyte globulin and etanercept induction, islet culture, heparinization, and intensive insulin therapy with the same low-dose tacrolimus and sirolimus maintenance immunosuppression as in the Edmonton protocol. To determine whether CIT07 improves engrafted islet β-cell mass, our center measured β-cell secretory capacity from glucose-potentiated arginine tests at days 75 and 365 after transplantation and compared those results with the results previously achieved by our group using the Edmonton protocol and normal subjects. All subjects were insulin free, with CIT07 subjects receiving fewer islet equivalents from a median of one donor compared with two donors for Edmonton protocol subjects. The acute insulin response to glucose-potentiated arginine (AIRpot) was greater in the CIT07 protocol than in the Edmonton protocol and was less in both cohorts than in normal subjects, with similar findings for C-peptide. The CIT07 subjects who completed reassessment at day 365 exhibited increasing AIRpot by trend relative to that of day 75. These data indicate that engrafted islet β-cell mass is markedly improved with the CIT07 protocol, especially given more frequent use of single islet donors. Although several peritransplant differences may have each contributed to this improvement, the lack of deterioration in β-cell secretory capacity over time in the CIT07 protocol suggests that low-dose tacrolimus and sirolimus are not toxic to islets.
تدمد: 1939-327X
0012-1797
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f158e425a50f360420bdffa1c90b5fd9Test
https://doi.org/10.2337/db12-1802Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....f158e425a50f360420bdffa1c90b5fd9
قاعدة البيانات: OpenAIRE