SEPARATION OF BLAST CELL AND LYMPHOCYTE-T PROGENITORS IN THE BLOOD OF PATIENTS WITH ACUTE MYELOBLASTIC-LEUKEMIA

  • 1 January 1979
    • journal article
    • research article
    • Vol. 54  (1) , 186-195
Abstract
The peripheral blood of acute myeloblastic leukemia (AML) patients often contains large numbers of 2 distinct cell populations, both capable of forming colonies in culture under similar conditions. The 1st population consists of the precursors of blast cells and has specificity for AML; the 2nd population consists of T [thymus-derived] lymphocyte precursors, also found in normal blood. The 2 progenitor populations could be separated by exploiting the capacity of T lymphocyte (but not blasts) progenitors to form rosettes with sheep erythrocytes (E rosettes). After E-rosette formation, T lymphocyte precursors could be removed by centrifugation on Ficoll-Hypaque. Such separation had a number of consequences. Blast progenitors could be detected where unseparated mononuclear preparations yielded no colonies or only T lymphocyte colonies (20 of 21 patients). The stimulator requirements of the blast progenitors changed indicating that cell-cell interactions may take place between blast and T lymphocyte progenitors. It is feasible to characterize blast and T-lymphocyte precursors independently, even though they may coexist in peripheral blood. This may be important if progenitor properties are attributes contributing to the variance in outcome in AML.

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