Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Porcine Islet-Specific Tolerance Induced by the Combination of Anti-Lfa-1 and Anti-Cd154 Mabs Is Dependent on Pd-1 Publisher Pubmed



Arefanian H1, 2, 3 ; Tredget EB1 ; Mok DCM1 ; Ramji Q1 ; Rafati S1 ; Rodriguezbarbosa J4 ; Korbutt GS1 ; Rajotte RV1 ; Gill RG5 ; Rayat GR1
Authors
Show Affiliations
Authors Affiliations
  1. 1. Alberta Diabetes Institute, Surgical-Medical Research Institute, Department of Surgery, University of Alberta, Edmonton, AB, Canada
  2. 2. Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Pancreatic Islet Biology and Transplantation Unit, Dasman Diabetes Institute, Kuwait, Dasman, Kuwait
  4. 4. Institute of Biomedicine (Immunobiology), University of Leon, Campus de Vegazana s/n, Leon, Spain
  5. 5. Barbara Davis Center for Childhood Diabetes, University of Colorado, Aurora, CO, United States

Source: Cell Transplantation Published:2016


Abstract

We previously demonstrated that short-term administration of a combination of anti-LFA-1 and anti-CD154 monoclonal antibodies (mAbs) induces tolerance to neonatal porcine islet (NPI) xenografts that is mediated by regulatory T cells (Tregs) in B6 mice. In this study, we examined whether the coinhibitory molecule PD-1 is required for the induction and maintenance of tolerance to NPI xenografts. We also determined whether tolerance to NPI xenografts could be extended to allogeneic mouse or xenogeneic rat islet grafts since we previously demonstrated that tolerance to NPI xenografts could be extended to second-party NPI xenografts. Finally, we determined whether tolerance to NPI xenografts could be extended to allogeneic mouse or second-party porcine skin grafts. Diabetic B6 mice were transplanted with 2,000 NPIs under the kidney capsule and treated with short-term administration of a combination of anti-LFA-1 and anti-CD154 mAbs. Some of these mice were also treated simultaneously with anti-PD-1 mAb at >150 days posttransplantation. Spleen cells from some of the tolerant B6 mice were used for proliferation assays or were injected into B6 rag−/− mice with established islet grafts from allogeneic or xenogeneic donors. All B6 mice treated with anti-LFA-1 and anti-CD154 mAbs achieved and maintained normoglycemia until the end of the study; however, some mice that were treated with anti-PD-1 mAb became diabetic. All B6 rag−/− mouse recipients of first- and second-party NPIs maintained normoglycemia after reconstitution with spleen cells from tolerant B6 mice, while all B6 rag−/− mouse recipients of allogeneic mouse or xenogeneic rat islets rejected their grafts after cell reconstitution. Tolerant B6 mice rejected their allogeneic mouse or xenogeneic second-party porcine skin grafts while remaining normoglycemic until the end of the study. These results show that porcine islet-specific tolerance is dependent on PD-1, which could not be extended to skin grafts. © 2016 Cognizant, LLC.
Related Docs
Experts (# of related papers)