CD4 AND CD8 ANTIGEN COEXPRESSION - A FLOW CYTOMETRIC STUDY OF PERIPHERAL-BLOOD, BONE-MARROW, BODY-FLUID, AND SOLID LYMPHORETICULAR SPECIMENS

Citation
Eh. Nah et al., CD4 AND CD8 ANTIGEN COEXPRESSION - A FLOW CYTOMETRIC STUDY OF PERIPHERAL-BLOOD, BONE-MARROW, BODY-FLUID, AND SOLID LYMPHORETICULAR SPECIMENS, Archives of pathology and laboratory medicine, 121(4), 1997, pp. 381-384
Citations number
17
Categorie Soggetti
Pathology,"Medical Laboratory Technology","Medicine, Research & Experimental
Journal title
Archives of pathology and laboratory medicine
ISSN journal
00039985 → ACNP
Volume
121
Issue
4
Year of publication
1997
Pages
381 - 384
Database
ISI
SICI code
0003-9985(1997)121:4<381:CACAC->2.0.ZU;2-B
Abstract
Objective.-CD4 and CD8 antigen coexpression occurs not only on blastic T-cell malignancies, but also on a small subset of mature lymphocytes . The aim of this study was to determine the prevalence of this popula tion of cells and to identify features that can be used to differentia te them from T lymphoblasts. Design.-All specimens submitted to the cl inical flow cytometry laboratory from August 1, 1994, through July 31, 1995, were analyzed for CD4 and CD8 coexpression. Main Outcome Measur e.-Percentage of lymphocytes coexpressing the CD4 and CD8 antigens. Re sults.-Four percent (22/526) of all specimens contained a population o f CD4/CD8 coexpressing cells. Five cases represented CD4 and CD8 antig en expression on neoplastic cells. In 17 cases, the CD4/CD8 coexpressi ng cells appeared to represent a population of mature lymphocytes with a normal phenotype. The immature cells of T-cell acute lymphocytic le ukemia and lymphoblastic lymphoma represented a dominant uniform popul ation of cells demonstrating strong staining with both the CD4 and CD8 antigens. Cases containing a mature population of CD4/CD8 coexpressin g cells were characterized by fewer coexpressing cells and variable ex pression of CD8. There were cases where distinction of this population of mature CD4/CD8 coexpressing lymphoid cells from a blastic malignan cy was not possible using immunophenotyping alone. Conclusion.-Correla tion of clinical, morphologic, and immunophenotypic data is recommende d to prevent the misdiagnosis of subtle involvement by a blastic T-cel l malignancy.