IDENTIFICATION OF MALIGNANT-CELLS IN MULTIPLE-MYELOMA BONE-MARROW WITH IMMUNOGLOBULIN V-H GENE PROBES BY FLUORESCENT IN-SITU HYBRIDIZATION AND FLOW-CYTOMETRY

Because it has been difficult to identify and separate malignant cells in human lymphoid malignancies, we have developed a flow cytometry-based fluorescent in situ hybridization (FISH) technique using immunoglobulin (Ig) heavy chain variable region (V-H) gene probes. After obtaining the specific V-H gene sequence expressed by the multiple myeloma IM-9 cell line and the malignant cells in five multiple myeloma patients, sense and antisense biotinylated single-stranded RNA probes were prepared by transcription from the malignant clone's V-H DNA sequences. The cells from the IM-9 cell line and from the mononuclear bone marrow cells of multiple myeloma patients were fixed, hybridized with the above biotinylated RNA probes, incubated with streptavidin-phycoerythrin, and analyzed by FACS(R) analysis. The myeloma cells stained positive with their own specific antisense V-H biotinylated RNA probes, whereas sense and irrelevant antisense biotinylated probes demonstrated only background staining. Dilutional concentrations of the IM-9 cell line with normal bone marrow cells were also accurately quantitated by this procedure. The application of this technique will allow a more accurate assessment of tumor burden in patients with multiple myeloma and should permit an accurate method of tumor cell purification for clinical as well as biological studies. Furthermore, this technological advance should be equally effective at identifying specific V-H gene-expressing cells in other lymphoid malignancies, as well as in nonmalignant B cell disorders.