Literature DB >> 1355681

The fetus as an optimal donor and recipient of hemopoietic stem cells.

E D Zanjani1, J L Ascensao, A W Flake, M R Harrison, M Tavassoli.   

Abstract

In the present work we used allogeneic in utero transplantation of fetal stem cells in sheep and monkeys. Thus, both the donor and recipient cells had preimmune status. We showed engraftment of allogeneic stem cells in the tolerant environment of the host. The engrafted cells showed trilineage (lymphoid, erythroid and myeloid) expression of differentiation. Long term maintenance of these engrafted cells was observed. We also demonstrated that ex vivo incubation of donor cells with growth factor can enhance the engraftment. Moreover, we have shown that the engrafted cells respond to phlebotomy in the same manner as endogenous cells. We, therefore, conclude that (a) Preimmune fetuses are highly suitable for stem cell transplantation both as donors and recipients. (b) Engraftment can be modulated by brief maneuvers such as ex vivo manipulation. (c) Functionally, the engrafted cells can respond to hemopoietic stimuli in a similar manner as the endogenous cells. Implications of this transplantation system in clinical medicine is discussed. Everyone who is involved in organ transplantation must, sooner or later, come to grips with immunological barriers which establishes the individuality of each organism by recognizing "self" from "non-self". Transplanters must overcome this barrier, if allogeneic organ transplantation is to be successful. In the case of hemopoietic stem cells (HSC), where immunocompetent cells are transplanted, graft-vs-host disease (GVHD) may also be expected. Tolerance can be expected when the recipient is genetically immunodeficient, thus being unable to mount an immunological barrier.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1355681

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  6 in total

1.  Isolation and therapeutic potential of human haemopoietic stem cells.

Authors:  Andrew D Clark; Heather G Jørgensen; Joanne Mountford; Tessa L Holyoake
Journal:  Cytotechnology       Date:  2003-03       Impact factor: 2.058

2.  Soluble factor(s) produced by adult bone marrow stroma inhibit in vitro proliferation and differentiation of fetal liver BFU-E by inducing apoptosis.

Authors:  V Roy; C M Verfaillie
Journal:  J Clin Invest       Date:  1997-08-15       Impact factor: 14.808

3.  Temporal definition of haematopoietic stem cell niches in a large animal model of in utero stem cell transplantation.

Authors:  Christine Jeanblanc; Angelina Daisy Goodrich; Evan Colletti; Saloomeh Mokhtari; Christopher D Porada; Esmail D Zanjani; Graça Almeida-Porada
Journal:  Br J Haematol       Date:  2014-03-27       Impact factor: 6.998

4.  In utero transplanted human hepatocytes allow postnatal engraftment of human hepatocytes in pigs.

Authors:  James E Fisher; Joseph B Lillegard; Travis J McKenzie; Brian R Rodysill; Peter J Wettstein; Scott L Nyberg
Journal:  Liver Transpl       Date:  2013-03       Impact factor: 5.799

5.  In Utero Haematopoietic Stem Cell Transplantation (IUHSCT).

Authors:  Maria Concetta Renda; Aurelio Maggio
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-12-29       Impact factor: 2.576

Review 6.  Engineered Swine Models of Cancer.

Authors:  Adrienne L Watson; Daniel F Carlson; David A Largaespada; Perry B Hackett; Scott C Fahrenkrug
Journal:  Front Genet       Date:  2016-05-09       Impact factor: 4.599

  6 in total

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