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CD8 expression in a case of chronic lymphocytic leukemia with trisomy 12
M C Bayo Hanza1, M F Palacios, R Dourisboure
1Department of Immunología Oncológica, Instituto de Investigaciones Hematológicas 'Mariano R. Castex', Academia Nacional de Medicina, Buenos Aires, Argentina.
Insights
This study details a rare case of B-cell chronic lymphocytic leukemia (B-CLL) exhibiting T-cell marker CD8. Further research is needed to determine the prognostic significance of this B-CLL subtype.
Area of Science:
- Hematology
- Immunophenotyping
- Cancer Genetics
Background:
- B-cell chronic lymphocytic leukemia (B-CLL) is a common lymphoid malignancy.
- Typical B-CLL cells express B-cell markers and lack T-cell antigens.
- Aberrant antigen expression can occur in B-CLL, but T-cell marker expression is rare.
Observation:
- A case of B-CLL presented with unusual expression of the T-cell-associated antigen CD8.
- Two-color flow-cytometric analysis confirmed CD8 expression on neoplastic B-cells.
- Immunoglobulin heavy-chain gene rearrangement confirmed B-cell clonality, while T-cell receptor gene rearrangement was absent.
Findings:
- Ploidy analysis revealed a tetraploid cell population and a high S-phase fraction.
- Fluorescence in situ hybridization (FISH) detected trisomy 12 in the B-CLL cells.
- The aberrant CD8 expression in this B-CLL case suggests a potential distinct subtype.
Implications:
- This case highlights the phenotypic heterogeneity within B-CLL.
- Trisomy 12 and a high S-phase fraction may be associated with this CD8-expressing B-CLL subtype.
- Further studies on additional cases are crucial to establish the clinical and prognostic implications of CD8 expression in B-CLL.
Abstract:
We report a case of B-cell chronic lymphocytic leukemia (B-CLL) with aberrant expression of the T-cell-associated antigen CD8, as revealed by two-color flow-cytometric analysis. DNA studies showed immunoglobulin heavy-chain gene rearrangement, but not of gamma-chain T-cell receptor, confirming the B-cell origin of the neoplastic cells. Ploidy analysis showed a tetraploid population and high S-phase fraction. B-CLL cells also carried trisomy 12, detected by fluorescence in situ hybridization. The identification of more cases with the same features would be necessary to establish the prognosis of this subtype of B-CLL.
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