F. Bertolini et al., HEMATOPOIETIC STEM-CELLS FROM DIFFERENT SOURCES - BIOLOGICAL AND TECHNICAL ASPECTS, Bone marrow transplantation, 21, 1998, pp. 5-7
Hematopoietic stem cell (HSC) enumeration is crucial to predict the en
graftment potential of a given HSC collection, and currently involves
the surrogate count of nucleated cells, CFU or CD34(+) cells. However,
there is raising evidence that CFU are HSC involved in shortterm but
not in long-term reconstitution, and that only a small fraction of all
CD34(+) cells have long term multilineage engraftment potential, In t
his regard, there is evidence that cord blood (CB), bone marrow (BM) a
nd peripheral blood (PB) derived HSC are highly heterogeneous for a nu
mber of antigens useful for HSC enumeration by flow cytometry, Moreove
r, there is a raising evidence that a CD34(-) human HSC might exist, T
he CD34(-) HSC has been already described in animals and in human Hoec
hst 33342 negative HSC, This notwithstanding, clinical data have clear
ly demonstrated that purified allogeneic CD34(+) cells can reconstitut
e the myeloid and the lymphoid lineages in myeloablated recipients. In
the lack of a suitable marker for CD34(-) HSC enumeration, it is hard
to predict the role of CD34(-) HSC in hematopoietic reconstitution af
ter transplantation, On the other hand, these cells might be a better
target for HSC expansion and gene transfer.