VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...
VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...
VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...
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THE BIOLOGY 0FCD34.<br />
D. Robert Sutherland and Armand Keating<br />
ONCOLOGY RESEARCH, AND THE UNIVERSITY OF TORONTO<br />
AUTOLOGOUS BONE MARROW TRANSPLANT PROGRAM, THE<br />
TORONTO HOSPITAL, TORONTO, CANADA.<br />
INTRODUCTION<br />
The CD34 antigen is of interest because it is the only molecule identified to<br />
date whose expression within the blood system, is restricted to a small number<br />
of primitive progenitor cells in the bone marrow (BM). The availability of CD34<br />
antibodies has greatly aided the development of techniques for the enrichment<br />
of primitive progenitor cells for a variety of studies of hematopoiesis in vitro.<br />
Additionally, the use of CD34 antibodies for the 'positive selection' of hematopoietic<br />
stem/progenitor cells represents an alternative strategy to 'purging' for<br />
the large-scale manipulation of cells prior to transplantation. The availability of<br />
pure populations of the most primitive hematopoietic progenitor cells may also<br />
facilitate the development of genetic techniques for the repair of specific blood<br />
cell disorders. Though its precise function remains unknown, the pattern of expression<br />
of the the CD34 structure suggests that it plays an important role in<br />
early hematopoiesis.<br />
SEROLOGY AND EPITOPE MAPPING STUDIES<br />
All seven antibodies, MY10, B1.3C5,12.8,115.2, ICH3, TUK3, and QBEND<br />
10, assigned to the CD34 cluster ( n<br />
, identify an antigen which is expressed on 1-<br />
3% of normal BM cells. This population has been shown to include virtually all<br />
unipotent, and multipotent myeloid progenitors as well as pre-CFU. Primitive T<br />
and B lymphocyte precursors and leukemias of primitive myeloid and lymphoid<br />
lineages also express CD34. Significantly, CD34+ BM cells can reconstitute<br />
all lineages of the hematopoietic system in lethally-irradiated baboons and rhesus<br />
monkeys, suggesting, that the 'stem cells' responsible for long-term reconstitution<br />
of hematopoiesis, express the CD34 antigen (see 2<br />
and refs therein). This<br />
population is also capable of reconstituting hematopoiesis in humans