Open AccessEnumeration of cytoplasmic μ immunoglobulin positive acute lymphoblastic leukemia cells by flow cytometry: Comparison with fluorescence microscopy
Author(s) -
Zipf T. F.,
Bryant L. D.,
Koskowich G. N.,
MacGregor S. E.,
Chin L.,
Johnson H.
Publication year - 1984
Publication title -
cytometry
Language(s) - English
Resource type - Journals
eISSN - 1097-0320
pISSN - 0196-4763
DOI - 10.1002/cyto.990050609
Subject(s) - flow cytometry , fluorescence microscope , antibody , enumeration , cytoplasm , phenotype , biology , immunophenotyping , fluorescence , lymphoblastic leukemia , microbiology and biotechnology , direct fluorescent antibody , cytometry , immunology , leukemia , pathology , medicine , biochemistry , gene , physics , mathematics , quantum mechanics , combinatorics
The pre‐B phenotype of childhood acute lymphoblastic leukemia, in which the μ immunoglobulin molecule is expressed in the cytoplasm of the blast cells, has been shown to have independent prognostic significance. Patients with this phenotype of the disease tend to have a poorer outcome on contemporary treatment regimens than do those with the other B‐precursor pheonotypes. For these clinical studies, the detection of the pre‐B phenotype has depended upon fluorescent‐microscope based techniques. A flow‐cytometry based technique for the detection of the cytoplasmic μ immunoglobulin molecule is presented here and the results compared in detail with those of fluorescent microscopy. The results show that the two techniques are equivalent. The flow cytometry method has the advantage of a standardized control, is less labor intensive, and is observer‐independent.