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- W2898845627 abstract "Purpose of review The aim of this study was to review the recent progress in xenotransplantation achieved through genetic engineering and discuss the potential of tolerance induction to overcome remaining barriers to extended xenograft survival. Recent findings The success of life-saving allotransplantation has created a demand for organ transplantation that cannot be met by the supply of human organs. Xenotransplantation is one possible solution that would allow for a nearly unlimited supply of organs. Recent genetic engineering of swine has decreased the reactivity of preformed antibodies to some, but not all, potential human recipients. Experiments using genetically modified swine organs have now resulted in survival of life-supporting kidneys for over a year. However, the grafts show evidence of antibody-mediated rejection on histology, suggesting additional measures will be required for further extension of graft survival. Tolerance induction through mixed chimerism or thymic transplantation across xenogeneic barriers would be well suited for patients with a positive crossmatch to genetically modified swine or relatively negative crossmatches to genetically modified swine, respectively. Summary This review highlights the current understanding of the immunologic processes in xenotransplantation and describes the development and application of strategies designed to overcome them from the genetic modification of the source animal to the induction of tolerance to xenografts." @default.
- W2898845627 created "2018-11-09" @default.
- W2898845627 creator A5003679165 @default.
- W2898845627 creator A5021758948 @default.
- W2898845627 creator A5056437755 @default.
- W2898845627 date "2018-12-01" @default.
- W2898845627 modified "2023-09-26" @default.
- W2898845627 title "Xenotransplantation tolerance: applications for recent advances in modified swine" @default.
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- W2898845627 doi "https://doi.org/10.1097/mot.0000000000000585" @default.
- W2898845627 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7010353" @default.
- W2898845627 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30379724" @default.
- W2898845627 hasPublicationYear "2018" @default.
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