Cargando…
The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation
There is a critical shortage of organs, cells, and corneas from deceased human donors worldwide. There are also shortages of human blood for transfusion. A potential solution to all of these problems is the transplantation of organs, cells, and corneas from a readily available animal species, such a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Department of Journal of Biomedical Research
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721033/ https://www.ncbi.nlm.nih.gov/pubmed/23885264 http://dx.doi.org/10.7555/JBR.27.20130063 |
_version_ | 1782278029630767104 |
---|---|
author | Cooper, David K.C. Hara, Hidetaka Ezzelarab, Mohamed Bottino, Rita Trucco, Massimo Phelps, Carol Ayares, David Dai, Yifan |
author_facet | Cooper, David K.C. Hara, Hidetaka Ezzelarab, Mohamed Bottino, Rita Trucco, Massimo Phelps, Carol Ayares, David Dai, Yifan |
author_sort | Cooper, David K.C. |
collection | PubMed |
description | There is a critical shortage of organs, cells, and corneas from deceased human donors worldwide. There are also shortages of human blood for transfusion. A potential solution to all of these problems is the transplantation of organs, cells, and corneas from a readily available animal species, such as the pig, and the transfusion of red blood cells from pigs into humans. However, to achieve these ends, major immunologic and other barriers have to be overcome. Considerable progress has been made in this respect by the genetic modification of pigs to protect their tissues from the primate immune response and to correct several molecular incompatibilities that exist between pig and primate. These have included knockout of genes responsible for the expression of major antigenic targets for primate natural anti-pig antibodies, insertion of human complement- and coagulation-regulatory transgenes, and knockdown of swine leukocyte antigens that stimulate the primate's adaptive immune response. As a result of these manipulations, the administration of novel immunosuppressive agents, and other innovations, pig hearts have now functioned in baboons for 6-8 months, pig islets have maintained normoglycemia in diabetic monkeys for > 1 year, and pig corneas have maintained transparency for several months. Clinical trials of pig islet transplantation are already in progress. Future developments will involve further genetic manipulations of the organ-source pig, with most of the genes that are likely to be beneficial already identified. |
format | Online Article Text |
id | pubmed-3721033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Editorial Department of Journal of Biomedical Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-37210332013-07-24 The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation Cooper, David K.C. Hara, Hidetaka Ezzelarab, Mohamed Bottino, Rita Trucco, Massimo Phelps, Carol Ayares, David Dai, Yifan J Biomed Res Invited Review There is a critical shortage of organs, cells, and corneas from deceased human donors worldwide. There are also shortages of human blood for transfusion. A potential solution to all of these problems is the transplantation of organs, cells, and corneas from a readily available animal species, such as the pig, and the transfusion of red blood cells from pigs into humans. However, to achieve these ends, major immunologic and other barriers have to be overcome. Considerable progress has been made in this respect by the genetic modification of pigs to protect their tissues from the primate immune response and to correct several molecular incompatibilities that exist between pig and primate. These have included knockout of genes responsible for the expression of major antigenic targets for primate natural anti-pig antibodies, insertion of human complement- and coagulation-regulatory transgenes, and knockdown of swine leukocyte antigens that stimulate the primate's adaptive immune response. As a result of these manipulations, the administration of novel immunosuppressive agents, and other innovations, pig hearts have now functioned in baboons for 6-8 months, pig islets have maintained normoglycemia in diabetic monkeys for > 1 year, and pig corneas have maintained transparency for several months. Clinical trials of pig islet transplantation are already in progress. Future developments will involve further genetic manipulations of the organ-source pig, with most of the genes that are likely to be beneficial already identified. Editorial Department of Journal of Biomedical Research 2013-07 2013-06-12 /pmc/articles/PMC3721033/ /pubmed/23885264 http://dx.doi.org/10.7555/JBR.27.20130063 Text en © 2013 by the Journal of Biomedical Research. All rights reserved. |
spellingShingle | Invited Review Cooper, David K.C. Hara, Hidetaka Ezzelarab, Mohamed Bottino, Rita Trucco, Massimo Phelps, Carol Ayares, David Dai, Yifan The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
title | The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
title_full | The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
title_fullStr | The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
title_full_unstemmed | The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
title_short | The potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
title_sort | potential of genetically-engineered pigs in providing an alternative source of organs and cells for transplantation |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721033/ https://www.ncbi.nlm.nih.gov/pubmed/23885264 http://dx.doi.org/10.7555/JBR.27.20130063 |
work_keys_str_mv | AT cooperdavidkc thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT harahidetaka thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT ezzelarabmohamed thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT bottinorita thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT truccomassimo thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT phelpscarol thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT ayaresdavid thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT daiyifan thepotentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT cooperdavidkc potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT harahidetaka potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT ezzelarabmohamed potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT bottinorita potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT truccomassimo potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT phelpscarol potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT ayaresdavid potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation AT daiyifan potentialofgeneticallyengineeredpigsinprovidinganalternativesourceoforgansandcellsfortransplantation |