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Updated: Aug 15, 2026

Flow Cytometry to Estimate Leukemia Stem Cells in Primary Acute Myeloid Leukemia and in Patient-derived-xenografts, at Diagnosis and Follow Up
Published on: March 26, 2018
Lymphomas: membrane markers and cell flow cytometric diagnosis
Lymphocytes are characterized by membrane markers which, in part, reflect biological and functional activity. This is particularly true for T lymphocyte subsets identified by monoclonal antibodies. The B lymphocytes can be identified but in a more general manner. It has been proposed that the use of these markers will aid in the differential diagnosis of a variety of lymphomas. The objective of this work was to evaluate the use of monoclonal antibodies (MAb-s) and surface immunoglobulin (sIg) analysis in a cell flow cytometer (CFC) as methods to identify and classify lymphomas. The cell flow cytometric findings were then evaluated in light of the histopathologic diagnosis (HPD). Fifty-eight (58) patients with a variety of lymphomas and benign lymph node disorders were studied. Lymph node tissue samples were obtained after surgical removal and appropriately prepared for evaluation in a CFC. Results showed that the variety of hyperplasias and reactive follicular lymphadenopathies could not be characterized by the technique or application of CFC alone. Both B cell and T cell lymphomas could be recognized and differentiated by MAb-s and/or light chain monotypism using sIg's in a CFC, but morphologic and clinical information were required for diagnostic confirmation. Hodgkin's disease could not be identified by CFC because of the lack of a specific identifiable marker. Cell flow cytometry provides an easy and rapid adjunct to the diagnosis of a variety of lymphomas. At the present time, membrane markers in cell suspensions from tissues (lymph nodes) identified by MAb-s and sIg's in a CFC cannot be used to provide definitive diagnoses for reactive lymphadenopathies, Hodgkin's disease or some classes of lymphomas.
Lymphocytes are characterized by membrane markers which, in part, reflect biological and functional activity. This is particularly true for T lymphocyte subsets identified by monoclonal antibodies. The B lymphocytes can be identified but in a more general manner. It has been proposed that the use of these markers will aid in the differential diagnosis of a variety of lymphomas. The objective of this work was to evaluate the use of monoclonal antibodies (MAb-s) and surface immunoglobulin (sIg) analysis in a cell flow cytometer (CFC) as methods to identify and classify lymphomas. The cell flow cytometric findings were then evaluated in light of the histopathologic diagnosis (HPD). Fifty-eight (58) patients with a variety of lymphomas and benign lymph node disorders were studied. Lymph node tissue samples were obtained after surgical removal and appropriately prepared for evaluation in a CFC. Results showed that the variety of hyperplasias and reactive follicular lymphadenopathies could not be characterized by the technique or application of CFC alone. Both B cell and T cell lymphomas could be recognized and differentiated by MAb-s and/or light chain monotypism using sIg's in a CFC, but morphologic and clinical information were required for diagnostic confirmation. Hodgkin's disease could not be identified by CFC because of the lack of a specific identifiable marker. Cell flow cytometry provides an easy and rapid adjunct to the diagnosis of a variety of lymphomas. At the present time, membrane markers in cell suspensions from tissues (lymph nodes) identified by MAb-s and sIg's in a CFC cannot be used to provide definitive diagnoses for reactive lymphadenopathies, Hodgkin's disease or some classes of lymphomas.

