Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation
Therapies that promote tolerance will improve outcomes in solid organ transplantation by eliminating the need for long-term immunosuppression. This thesis investigates two possible tolerance induction mechanisms: rapamycin induced expression of regulatory T cells and re-education of the immune syste...
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ndltd-LACETR-oai-collectionscanada.gc.ca-OTU.1807-429312014-01-11T03:44:24ZInduction of Tolerance: Mechanisms and Implications for Clinical TransplantationShyu, Wendy Huei-PingTransplantationTolerance0982Therapies that promote tolerance will improve outcomes in solid organ transplantation by eliminating the need for long-term immunosuppression. This thesis investigates two possible tolerance induction mechanisms: rapamycin induced expression of regulatory T cells and re-education of the immune system using syngeneic hematopoietic stem cell transplantation. Fibrinogen-like protein 2, a effector molecule of regulatory T cells, was also determined as a key mediator in the tolerance induction pathway as depletion of fibrinogen-like protein 2 lead to allograft rejection. The feasibility of using syngeneic hematopoietic stem cells for inducing allograft tolerance was studied by setting up a murine heart and bone marrow transplant model. Syngeneic T-depleted bone marrow transplantation resulted in a slight prolongation of the graft survival time compared to the animals reconstituted with total bone marrow cells. We provide compelling evidence to suggest that fibrinogen-like protein 2 and syngeneic hematopoietic stem cells can possibly be used to induce transplantation tolerance.Levy, Gary A.2013-112013-11-28T15:42:59ZNO_RESTRICTION2013-11-28T15:42:59Z2013-11-28Thesishttp://hdl.handle.net/1807/42931en_ca |
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Transplantation Tolerance 0982 |
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Transplantation Tolerance 0982 Shyu, Wendy Huei-Ping Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation |
description |
Therapies that promote tolerance will improve outcomes in solid organ transplantation by eliminating the need for long-term immunosuppression. This thesis investigates two possible tolerance induction mechanisms: rapamycin induced expression of regulatory T cells and re-education of the immune system using syngeneic hematopoietic stem cell transplantation. Fibrinogen-like protein 2, a effector molecule of regulatory T cells, was also determined as a key mediator in the tolerance induction pathway as depletion of fibrinogen-like protein 2 lead to allograft rejection. The feasibility of using syngeneic hematopoietic stem cells for inducing allograft tolerance was studied by setting up a murine heart and bone marrow transplant model. Syngeneic T-depleted bone marrow transplantation resulted in a slight prolongation of the graft survival time compared to the animals reconstituted with total bone marrow cells. We provide compelling evidence to suggest that fibrinogen-like protein 2 and syngeneic hematopoietic stem cells can possibly be used to induce transplantation tolerance. |
author2 |
Levy, Gary A. |
author_facet |
Levy, Gary A. Shyu, Wendy Huei-Ping |
author |
Shyu, Wendy Huei-Ping |
author_sort |
Shyu, Wendy Huei-Ping |
title |
Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation |
title_short |
Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation |
title_full |
Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation |
title_fullStr |
Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation |
title_full_unstemmed |
Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation |
title_sort |
induction of tolerance: mechanisms and implications for clinical transplantation |
publishDate |
2013 |
url |
http://hdl.handle.net/1807/42931 |
work_keys_str_mv |
AT shyuwendyhueiping inductionoftolerancemechanismsandimplicationsforclinicaltransplantation |
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