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Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases

OBJECTIVE: To assess long-term metabolic and immunological follow-up of microencapsulated human islet allografts in nonimmunosuppressed patients with type 1 diabetes (T1DM). RESEARCH DESIGN AND METHODS: Four nonimmunosuppressed patients, with long-standing T1DM, received intraperitoneal transplant (...

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Autores principales: Basta, Giuseppe, Montanucci, Pia, Luca, Giovanni, Boselli, Carlo, Noya, Giuseppe, Barbaro, Barbara, Qi, Meirigeng, Kinzer, Katie P., Oberholzer, José, Calafiore, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198271/
https://www.ncbi.nlm.nih.gov/pubmed/21926290
http://dx.doi.org/10.2337/dc11-0731
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author Basta, Giuseppe
Montanucci, Pia
Luca, Giovanni
Boselli, Carlo
Noya, Giuseppe
Barbaro, Barbara
Qi, Meirigeng
Kinzer, Katie P.
Oberholzer, José
Calafiore, Riccardo
author_facet Basta, Giuseppe
Montanucci, Pia
Luca, Giovanni
Boselli, Carlo
Noya, Giuseppe
Barbaro, Barbara
Qi, Meirigeng
Kinzer, Katie P.
Oberholzer, José
Calafiore, Riccardo
author_sort Basta, Giuseppe
collection PubMed
description OBJECTIVE: To assess long-term metabolic and immunological follow-up of microencapsulated human islet allografts in nonimmunosuppressed patients with type 1 diabetes (T1DM). RESEARCH DESIGN AND METHODS: Four nonimmunosuppressed patients, with long-standing T1DM, received intraperitoneal transplant (TX) of microencapsulated human islets. Anti-major histocompatibility complex (MHC) class I–II, GAD65, and islet cell antibodies were measured before and long term after TX. RESULTS: All patients turned positive for serum C-peptide response, both in basal and after stimulation, throughout 3 years of posttransplant follow-up. Daily mean blood glucose, as well as HbA(1c) levels, significantly improved after TX, with daily exogenous insulin consumption declining in all cases and being discontinued, just transiently, only in patient 4. Anti-MHC class I–II and GAD65 antibodies all tested negative at 3 years after TX. CONCLUSIONS: The grafts did not elicit any immune response, even in the cases where more than one preparation was transplanted, as a unique finding, compatible with encapsulation-driven “bioinvisibility” of the grafted islets. This result had never been achieved with the recipient’s general immunosuppression.
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spelling pubmed-31982712012-11-01 Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases Basta, Giuseppe Montanucci, Pia Luca, Giovanni Boselli, Carlo Noya, Giuseppe Barbaro, Barbara Qi, Meirigeng Kinzer, Katie P. Oberholzer, José Calafiore, Riccardo Diabetes Care Original Research OBJECTIVE: To assess long-term metabolic and immunological follow-up of microencapsulated human islet allografts in nonimmunosuppressed patients with type 1 diabetes (T1DM). RESEARCH DESIGN AND METHODS: Four nonimmunosuppressed patients, with long-standing T1DM, received intraperitoneal transplant (TX) of microencapsulated human islets. Anti-major histocompatibility complex (MHC) class I–II, GAD65, and islet cell antibodies were measured before and long term after TX. RESULTS: All patients turned positive for serum C-peptide response, both in basal and after stimulation, throughout 3 years of posttransplant follow-up. Daily mean blood glucose, as well as HbA(1c) levels, significantly improved after TX, with daily exogenous insulin consumption declining in all cases and being discontinued, just transiently, only in patient 4. Anti-MHC class I–II and GAD65 antibodies all tested negative at 3 years after TX. CONCLUSIONS: The grafts did not elicit any immune response, even in the cases where more than one preparation was transplanted, as a unique finding, compatible with encapsulation-driven “bioinvisibility” of the grafted islets. This result had never been achieved with the recipient’s general immunosuppression. American Diabetes Association 2011-11 2011-10-15 /pmc/articles/PMC3198271/ /pubmed/21926290 http://dx.doi.org/10.2337/dc11-0731 Text en © 2011 by the American Diabetes Association. https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ (https://creativecommons.org/licenses/by-nc-nd/3.0/) for details.
spellingShingle Original Research
Basta, Giuseppe
Montanucci, Pia
Luca, Giovanni
Boselli, Carlo
Noya, Giuseppe
Barbaro, Barbara
Qi, Meirigeng
Kinzer, Katie P.
Oberholzer, José
Calafiore, Riccardo
Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases
title Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases
title_full Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases
title_fullStr Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases
title_full_unstemmed Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases
title_short Long-Term Metabolic and Immunological Follow-Up of Nonimmunosuppressed Patients With Type 1 Diabetes Treated With Microencapsulated Islet Allografts: Four cases
title_sort long-term metabolic and immunological follow-up of nonimmunosuppressed patients with type 1 diabetes treated with microencapsulated islet allografts: four cases
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198271/
https://www.ncbi.nlm.nih.gov/pubmed/21926290
http://dx.doi.org/10.2337/dc11-0731
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