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Autologous Bone Marrow Transplantation - Blog Science Connections

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Using a Liquid Cell Culture Assay to Measure<br />

In Vitro Elimination of Burkitt's Cells From<br />

<strong>Bone</strong> <strong>Marrow</strong><br />

/. Philip, M. C. Favrot, V. Combaret, J. G Laurent, B. Kremens,<br />

and T. Philip<br />

We have developed a liquid cell culture assay that enables the growth of<br />

Burkitt's lymphoma (BL) cells, whose culture is either Epstein-Barr virus (EBV)<br />

positive or negative, from cytologically normal bone marrow. As previously<br />

reported, we currently use such an assay in our patients' follow-up to detect<br />

minimal bone marrow involvement (1). This assay has permitted us to show<br />

that 40% of patients in partial remission or in relapse have bone marrow<br />

involvement, even if their bone marrow is cytologically normal (2).<br />

We describe here how we have modified this assay to refine and quantify<br />

the purging procedure. In artificial models when irradiated allogeneic bone<br />

marrow is contaminated with BL cell lines, this liquid culture assay enables the<br />

growth of as few as one BL cell in 4 x 10 6<br />

normal bone marrow cells in a wide<br />

range of BL cell lines. This culture assay also is useful in newly established<br />

EBV-negative or EBV-positive lines from our Caucasian patients who are<br />

candidates for autologous bone marrow transplantation (ABMT) (3). More<br />

recently, the assay has been used to quantify the elimination of fresh Burkitt's<br />

cells from our patients' autologous bone marrow and to evaluate the quality of<br />

therapeutic purging procedures, either in a preclinical assay or in the clinical<br />

procedure itself, and we will specially emphasize this last point here.<br />

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