Select your timezone:

Islet transplantation, xeno and organoids

Thursday October 26, 2023 - 15:20 to 16:20

Room: Indigo 204

118.5 Insulin independence after intraportal islet transplantation in patients with kidney allograft and type 1 diabetes mellitus.

William Lin, United States

Post-Doctoral Researcher
Transplant Surgery
University of Chicago

Abstract

Insulin independence after intraportal islet transplantation in patients with kidney allograft and type 1 diabetes mellitus

Mateusz Ogledzinski1, William Lin1, Sarah Gondek 1, Kamila Milejczyk1, Braden Juengel 1, Piotr J Bachul1, Lindsay Basto1, Laurencia Perea1, Ling-jia Wang1, Martin Tibudan1, Rolf Barth1, John J Fung1, Piotr Witkowski1.

1Surgery, University of Chicago, Chicago, IL, United States

Background: Islet after kidney transplantation (IAK) could be an alternative to pancreas transplant in patients with T1DM but clinical outcomes of IAK are inconsistent and the experience is very limited.  Here, we present our pilot study of islet after kidney transplantation, which provided insulin independence and optimal blood glucose control.  

Material: Islet transplantation was performed 5 (2-5.5) years after initial kidney transplant in four T1DM patients and at a median age of 50(45-59) with median BMI of 25(23-26) and median HbA1c of 8.6(6.8-10.2). Median serum creatinine and eGFR were 1.5 (0.9-2.1)and 50 (31-91), respectively. All those patients received basiliximab induction and standard for kidney transplant maintenance immunosuppression.  One additional patient received islets infusion  2 days after kidney transplantation with anti-thymocyte globulin induction. Etanercept was administered subcutaneously as peri-transplant anti-inflammatory therapy.  

Results: Single islet infusion led to insulin independence in all five patients. Currently four patients remain insulin independent with serum HbA1c <6 for 24, 15, 11 and 4 months after the transplant. Another patient with a high BMI of 30 required a second islet transplant four months after the first one, maintaining insulin independence for the subsequent 5 years. Patients achieved optimal clinical outcome with islet mass and donors comparable to those offered to islet transplant alone recipients with a mean IEQ transplanted of 396,000 (6,121 IEQ/k) and donor BMI 36 (33-37). None of the patients have experienced short or long term adverse events related to islet transplantation. Kidney graft function remained stable without progression of proteinuria. 

Conclusion: Islet after kidney transplantation allows for the restoration of insulin independence in type 1 diabetic patients without compromising kidney graft function.

The study was supported by the Dompe ́ Farmaceutici S.p.A. The authors would like to acknowledge the generosity and support of Dr. Martin Jendrisak and the entire team of the Gift of Hope Organ & Tissue Donor Network in Chicago, NJ Sharing Network, Lifebanc Ohio for providing the human pancreas tissues used in the present study. We also acknowledge support from the NIDDK P30 DK020595 and the Kovler Family Fund..

Organized by

Supported by

Hosted by


IPITA-IXA-CTRMS Joint Congress • San Diego, CA, USA • October 26-29, 2023
© 2024 IPITA-IXA-CTRMS 2023