Simultaneous Islet and Kidney Transplantation in Seven Patients With Type 1 Diabetes and End-Stage Renal Disease Using a Glucocorticoid-Free Immunosuppressive Regimen With Alemtuzumab Induction

  1. Jianming Tan,
  2. Shunliang Yang,
  3. Jinquan Cai,
  4. Junqi Guo,
  5. Lianghu Huang,
  6. Zhixian Wu,
  7. Jin Chen and
  8. Lianming Liao
  1. From the Organ Transplant Institute, Fuzhou General Hospital, Fuzhou, China
  1. Corresponding author: Jianming Tan, doctortjm{at}yahoo.com

Abstract

OBJECTIVE—The aim of this study was to evaluate the efficiency and safety of simultaneous islet and kidney transplantation in patients with type 1 diabetes and end-stage renal disease using a glucocorticoid-free immunosuppressive regimen with alemtuzumab induction.

RESEARCH DESIGN AND METHODS—Seven patients with type 1 diabetes and end-stage renal failure were transplanted with allogenic islets and kidneys procured from brain-dead donors. To prevent organ rejection, patients received alemtuzumab for induction immunosuppression, followed by sirolimus and tacrolimus. No glucocorticoids were given at any time.

RESULTS—The median duration of follow-up was 18.3 months (range 13–31). Kidney survival was 100%. Four patients became insulin independent at 1 year. The other three reduced insulin use to less than 25% of the amount required before transplantation. Serum C-peptide levels were significantly greater posttransplant in all patients, indicating continued islet function. No major procedure-related complications were observed.

CONCLUSIONS—Our results demonstrate that a steroid-free immunosuppressive regimen consisting of alemtuzumab, sirolimus, and tacrolimus is feasible for simultaneous islet and kidney transplantation. The question of whether this induction regimen is superior to more standard induction deserves large studies.

Footnotes

  • Published ahead of print at http://diabetes.diabetesjournals.org on 15 July 2008. Clinical trial reg. no. NCT00692562, clinicaltrials.gov.

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    • Accepted June 30, 2008.
    • Received March 14, 2008.
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