MUM1/IRF4 expression in the circulating compartment of chronic lymphocytic leukemia
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作者:
Craig, Fiona
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Univ Pittsburgh, Sch Med, Dept Pathol, Div Hematopathol, Pittsburgh, PA USAUniv Pittsburgh, Sch Med, Dept Pathol, Div Hematopathol, Pittsburgh, PA USA
Craig, Fiona
[1
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Soma, Lorinda
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Univ Pittsburgh, Sch Med, Dept Pathol, Div Hematopathol, Pittsburgh, PA USAUniv Pittsburgh, Sch Med, Dept Pathol, Div Hematopathol, Pittsburgh, PA USA
Soma, Lorinda
[1
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Melan, Melissa
[2
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Kant, Jeffrey
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Univ Pittsburgh, Sch Med, Dept Pathol, Div Mol Diagnost, Pittsburgh, PA USA
Univ Pittsburgh, Sch Med, Dept Human Genet, Pittsburgh, PA USAUniv Pittsburgh, Sch Med, Dept Pathol, Div Hematopathol, Pittsburgh, PA USA
Kant, Jeffrey
[2
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Swerdlow, Steven
[1
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机构:
[1] Univ Pittsburgh, Sch Med, Dept Pathol, Div Hematopathol, Pittsburgh, PA USA
[2] Univ Pittsburgh, Sch Med, Dept Pathol, Div Mol Diagnost, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Dept Human Genet, Pittsburgh, PA USA
MUM1/IRF4 is normally expressed in late germinal center/post germinal center B-cells. Previous studies of chronic lymphocytic leukemia in bone marrow and lymph node have demonstrated variable expression of MUM1/IRF4 and conflicting prognostic significance. In this study we evaluated MUM1/IRF4 expression in peripheral blood CLL cells utilizing Histogel cell blocks. MUM1/IRF4 was absent in 4/36 (11%) specimens. The remaining cases demonstrated variable intensity and proportion of positive cells: 20% positive 16/36 (44%), 20-50% positive 12/36 (33%), 50% 4/36 (11%). No correlation was identified between MUM1/IRF4 and percent of CD38 positive cells, CD38 status (+/-), ZAP-70 status (+/-), and IgVH mutational status. The variability in MUM1/IRF4 staining suggests a level of biologic complexity that is not adequately reflected in the current binary models of CLL pathobiology. This heterogeneity may reflect the role of MUM1/IRF4 as an effector and integrator of several lymphocyte activation pathways including antigenic and environmental stimuli.