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Autologous Bone Marrow Transplantation - Blog Science Connections

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CALLA-Negative Clonogenic Cultures in<br />

CALLA-Positive B-Cell Precursor Acute<br />

Lymphoblastic Leukemia<br />

Fatih M. CJckun, John H. Kersey, Daniel A Vallera,<br />

Norma K C. Ramsay, Kevin G. Waddick, and<br />

Kazimiera J. Gajl-Peczalska<br />

A variety of immunologic strategies is being evaluated for effective ex vivo<br />

purging of residual leukemic cells from autografts. The alternatives include<br />

treatment of marrow with monoclonal antibodies (MAbs) plus complement,<br />

with immunotoxins, and with MAbs linked to magnetic beads (1). For a MAb to<br />

be of therapeutic value in autologous bone marrow transplantation (ABMT) for<br />

acute lymphoblastic leukemia (ALL), it must be reactive with the majority of<br />

clonogenic ALL blasts in autografts. Choosing a MAb for ex vivo marrow<br />

purging has been exclusively based on the immunologic surface marker<br />

profiles of the bulk of marrow blasts at diagnosis or relapse. Given the high<br />

degree of heterogeneity in ALL, the immunophenotype of marrow blasts may<br />

not reliably predict the immunophenotype of clonogenic ALL cells. Currently,<br />

very little is known about the immunologic surface marker profiles of<br />

clonogenic blasts in ALL. The paucity of knowledge largely reflects the historic<br />

difficulties in cloning ALL blasts.<br />

To learn more about these cells, we have developed colony assays that<br />

enable us to culture leukemic cells of B lineage (2,3) and T lineage from freshly<br />

757

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