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Predictive factors of allosensitization after immunosuppressant withdrawal in recipients of long-term cultured islet cell grafts

Journal Contribution - Journal Article

Background: Islet transplantation has been reported to induce allosensitization in the majority of type 1 diabetic recipients of fresh or shortly incubated islet grafts prepared from one to three donors.

Methods: We examined the appearance of human leukocyte antigen (HLA) antibodies after withdrawal of immunosuppressants in 35 type 1 diabetic recipients of islet cell grafts prepared from a median of 6 donors (range, 2-11), cultured for longer periods, and characterized for their cellular composition. Immunosuppression consisted of antithymocyte globulin induction followed by mycophenolate mofetil plus calcineurin inhibitors (n=28, with 7 also receiving steroids) or sirolimus with (n=3) or without calcineurin inhibitors (n=4). Both the complement-dependent cytotoxicity (CDC) assay (class I) and the solid-phase flow-based Luminex method (class I and II) were used to identify HLA antibodies.

Results: Immunosuppressant withdrawal resulted in CDC positivity for class I antibodies in only 6% of patients. However, the majority became positive for class I antibodies (72%) or class II antibodies (72%) in the Luminex assay; positivity was not correlated to a higher number of donors or HLA mismatches, but with a lower [beta]-cell purity; use of steroids reduced de novo positivity for Luminex class I antibodies.

Conclusion: Allosensitization to cultured human islet cell grafts was low when assessed by CDC assay but high in Luminex. No correlation was found with the number of donors but risk was higher for grafts with lower [beta]-cell purity.
Journal: Transplantation
ISSN: 0041-1337
Volume: 96
Pages: 162-169
Publication year:2013
Keywords:islet transplantation
  • WoS Id: 000330378600016
  • DOI: https://doi.org/10.1097/tp.0b013e3182977afc
  • Scopus Id: 84880533755
  • ORCID: /0000-0003-0228-699X/work/60677834
  • ORCID: /0000-0002-9007-6177/work/60767417
  • ORCID: /0000-0002-8671-4527/work/61349255
  • ORCID: /0000-0002-6440-2485/work/61423308
  • ORCID: /0000-0001-5758-9547/work/76554332
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