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Comprehensive Protocol to Sample and Process Bone Marrow for Measuring Measurable Residual Disease and Leukemic Stem Cells in Acute Myeloid Leukemia
Published on: March 5, 2018
Flow cytometric analysis of phenotypes and naïve/memory/effector T-cell subsets of T-cell large granular lymphocytic
Haipeng Shao1, Ning Dong2, Richard Shao3
1Department of Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Abstract:
This study investigates T-cell antigen expression and functional subsets in T-cell large granular lymphocytic leukemia (T-LGLL) cells by flow cytometry. The leukemic T-LGLs frequently showed expressions of CD57, dim CD2, CD5 and CD7, and more likely CD16 and HLA-DR, compared with reactive/benign T-LGLs. The leukemic T-LGLs were composed predominantly of CD8+ effector memory with re-acquired CD45RA cells (TEMRA, median: 89.6%), with TEMRA cells in >70% of the T-LGLs in 82% of the cases. A small subset of T-LGLL cases showed predominance of CD8+ naïve cells (TN, 2%), CD8+ effector memory cells (TEM, 4%) and transition states between different functional subsets (10%). In contrast, reactive/benign T-LGLs in the control group showed more variable expression of CD62L and CD45RA and more frequent functional subsets other than TEMRA cells. There is significant overlap between leukemic T-LGLs and reactive/benign T-LGLs in terms of common T-cell antigen expression and naïve/memory/effector T-cell subsets.

