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The susceptibility of baboons to the novel immunosuppressant, FTY720

Bibliography: leaves 109-118.

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Bibliographic Details
Main Author: Semple, P L
Other Authors: Quesniaux, Valerie
Format: Thesis
Language:English
Published: Department of Medicine 2014
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access_status_str Open Access
author Semple, P L
author2 Quesniaux, Valerie
author_browse Quesniaux, Valerie
Semple, P L
author_facet Quesniaux, Valerie
Semple, P L
author_sort Semple, P L
collection Thesis
description Bibliography: leaves 109-118.
format Thesis
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institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:26.116Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
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publisher Department of Medicine
publisherStr Department of Medicine
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/3463 The susceptibility of baboons to the novel immunosuppressant, FTY720 Semple, P L Quesniaux, Valerie Medicine Bibliography: leaves 109-118. Since there is a major scarcity of donor organs world-wide, the experimental search for human organs has focused on two alternatives; mechanical devices and cross-species transplants. The use of mechanical devices as substitute organs is understandably limited due to complications from trying to duplicate the function of complex organs such as the liver. This has resulted in a renewed interest in xenotransplantation. Organs from non-human primates would arguably be the organs of choice but ethical consideration prevents this. The transplantation of organs from pigs or sheep to humans i.e. xenotransplants, results in hyperacute rejection. The development of immunosuppressive agents such as Cyc1osporine A and Tacrolimus have significantly improved the survival of organ transplants. However, although there is a good 1-5 year survival, the recurrent problem of chronic rejection still remains, and unresponsiveness to allografts has never been induced by these immunosuppressive agents. More importantly, the presence of adverse side effects including immunological complications and drug toxicity e.g. nephrotoxicity, remains a serious problem. Since the drugs currently available for allotransplantation preferably target T -cells, and are therefore unlikely to be sufficient for xenotransplantation where there is a strong B-cell driven response, there is a need for new immunosuppressive agents. FTY720 (2 amino-2-(2-[ 4-octylphenyl] ethyl)-1,3-propanediol hydrochloride), a novel, immunosuppressive drug active in rodent and dog transplantation models, has shown no toxic side effects in pre-clinical studies although no long-term patient studies exist. 2014-07-29T09:10:28Z 2014-07-29T09:10:28Z 2000 Master Thesis Masters MSc http://hdl.handle.net/11427/3463 eng application/pdf Department of Medicine Faculty of Health Sciences University of Cape Town
spellingShingle Medicine
Semple, P L
The susceptibility of baboons to the novel immunosuppressant, FTY720
thesis_degree_str Master's
title The susceptibility of baboons to the novel immunosuppressant, FTY720
title_full The susceptibility of baboons to the novel immunosuppressant, FTY720
title_fullStr The susceptibility of baboons to the novel immunosuppressant, FTY720
title_full_unstemmed The susceptibility of baboons to the novel immunosuppressant, FTY720
title_short The susceptibility of baboons to the novel immunosuppressant, FTY720
title_sort susceptibility of baboons to the novel immunosuppressant fty720
topic Medicine
url http://hdl.handle.net/11427/3463
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