The purified CD34(+) cell fraction has been used for hematopoietic stem cell transplantation since they were demonstrated to have long-term reconstituting ability. Therefore, the potential effects of CD34(-) stem cells on the clinical course have been a major concern in recipients of CD34(+)-selected transplantation. To address this concern, we used an in vitro assay to determine whether transplant recipients have CD34- precursor population. Lin(-)CD34(-) cells were isolated from bone marrow cells in 11 transplant recipients including four CD34-selected transplantations, six standard bone marrow transplantations, and one T cell-depleted marrow transplantation. The frequency of the Lin-CD34- population in four CD34-enriched transplantation recipients was not different from those of normal donors or recipients of other modes of transplantation: 0.96 +/- 1.01% (mean +/- s.d., n = 4), 0.45 +/- 0.16% (n = 6), and 0.66 +/- 0.59% (n = 7), respectively. However, the Lin-CD34- population obtained from the recipients of CD34-enriched transplantation acquired neither CD34 expression nor colony-forming activity after 7 days of culture, whereas the cells from all the normal individuals and standard BMT recipients were able to differentiate into CD34+ cells accompanied by the emergence of colony-forming activity. We conclude that recipients of CD34-enriched transplantation appear to have defects in their CD34(-) precursor population. The clinical significance of these defects will be determined in a life-long follow-up of these patients.
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Ho, Jenny M.
Dobson, Stephanie M.
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Dobson, Stephanie M.
McLeod, Jessica
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
McLeod, Jessica
Voisin, Veronique
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Univ Toronto, Terrence Donnelly Ctr Cellular & Biomed Res, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Voisin, Veronique
Murison, Alex
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Murison, Alex
Kennedy, James
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Kennedy, James
Zandi, Sasan
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Univ Toronto, Lab Med & Pathobiol, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Zandi, Sasan
Eppert, Kolja
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McGill Univ, Res Inst, Ctr Hlth, Montreal, PQ, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Eppert, Kolja
Minden, Mark D.
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Univ Toronto, Div Med Oncol & Hematol, Princess Margaret Canc Ctr, Toronto, ON, Canada
Univ Toronto, Dept Med Biophys, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Minden, Mark D.
Lupien, Mathieu
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Univ Toronto, Dept Med Biophys, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Lupien, Mathieu
Dick, John E.
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Univ Toronto, Mol Genet, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Dick, John E.
Wang, Jean C. Y.
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Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
Univ Toronto, Dept Med, Toronto, ON, Canada
Dept Med, Div Med Oncol & Hematol, Toronto, ON, CanadaUniv Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada