Literature DB >> 11924916

Allogeneic transplantation using peripheral blood stem cells.

N H Russell1, J L Byrne.   

Abstract

Over the past 9 years there has been a remarkable increase in the use of peripheral blood stem cells (PBSC) for allogeneic transplantation, primarily for matched sibling transplants but also increasingly for unrelated donor transplantation. In 1999 over 50% of all sibling transplants and over 25% of unrelated donor transplants reported to the European Group for Blood and Marrow Transplantation (EBMT) used PBSC. The major reason for this increasing use of PBSC relates to the rapid haemopoietic recovery seen which mirrors the advantages of using PBSC in autologous transplantation. This improvement in engraftment is a consequence of the larger number of stem cells that can be collected from G-CSF-mobilized peripheral blood compared to bone marrow. Evidence from randomized trials now shows a survival advantage for the use of PBSC in patients with advanced leukaemia. The reason for this improved survival appears primarily to relate to a reduced risk of transplant-related mortality and, possibly, a reduced risk of relapse, However, these randomized studies have also confirmed that there is an increased risk of chronic graft-versus-host disease associated with PBSC transplantation and further follow-up is required to determine the long-term impact on outcome.

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Year:  2001        PMID: 11924916     DOI: 10.1053/beha.2001.0167

Source DB:  PubMed          Journal:  Best Pract Res Clin Haematol        ISSN: 1521-6926            Impact factor:   3.020


  3 in total

1.  An MHC-defined primate model reveals significant rejection of bone marrow after mixed chimerism induction despite full MHC matching.

Authors:  C P Larsen; A Page; K H Linzie; M Russell; T Deane; L Stempora; E Strobert; M C T Penedo; T Ward; R Wiseman; D O'Connor; W Miller; S Sen; K Singh; L S Kean
Journal:  Am J Transplant       Date:  2010-09-17       Impact factor: 8.086

2.  The human-sheep chimeras as a model for human stem cell mobilization and evaluation of hematopoietic grafts' potential.

Authors:  Graça Almeida-Porada; Christopher Porada; Nicole Gupta; Ali Torabi; David Thain; Esmail D Zanjani
Journal:  Exp Hematol       Date:  2007-10       Impact factor: 3.084

3.  Variant rs1801157 in the 3'UTR of SDF-1ß does not explain variability of healthy-donor G-CSF responsiveness.

Authors:  Miriam Schulz; Darja Karpova; Gabriele Spohn; Annette Damert; Erhard Seifried; Vera Binder; Halvard Bönig
Journal:  PLoS One       Date:  2015-03-24       Impact factor: 3.240

  3 in total

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