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PMID: 15714161 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Porcine hematopoietic progenitor cell transplantation in nonhuman primates: a review of progress.

Transplantation ·Vol. 79 ·No. 1 ·2005-01-15 ·Pages 1-9

Tseng YL, Tseng YL, Sachs DH, Cooper DK

Abstract

The critical shortage of human donor organs for transplantation would be overcome if a suitable animal, e.g., the pig, could be used as an organ source. There are, however, several immune barriers that have to date resulted in limited function of pig organs transplanted into nonhuman primates. It would be beneficial, and indeed may be essential, to induce a state of tolerance in the primate recipient to the pig organ. In allotransplantation, the successful transplantation of hematopoietic progenitor cells with the development of mixed chimerism is associated with the induction of tolerance toward a donor-specific organ. For some years, this approach has been explored in the pig-to-nonhuman primate model. This experience is briefly reviewed. The problems of natural and elicited anti-pig antibodies, recipient platelet adhesion to pig hematopietic progenitor cells, and the rapid removal of these cells by the host macrophage-phagocytic system are highlighted. Recent experience with the use of hematopoietic cells from pigs homozygous for alpha1,3-galactosyltransferase gene-knockout is reported.

MeSH Terms
Animals Galactosyltransferases/genetics Hematopoietic Stem Cell Transplantation Macaca fascicularis Papio Platelet Aggregation Swine Transplantation, Heterologous
Chemicals
Galactosyltransferases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tseng Yau-Lin
Transplantation Biology Research Center, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02129, USA.
Tseng Yan-Lin
Sachs David H
Cooper David K C
Article Info
Journal
Transplantation
Abbr.
Transplantation
ISSN
0041-1337
Published
2005-01-15
Pages
1-9
Language
English
Region
United States
NLM ID
0132144
Subset
IM
Grants
NIAID NIH HHS · 1P01 AI45897 · United States
Corrections
ErratumIn
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