Abstract |
The usefulness of flow cytometric variable β-chain repertoire (FC-Vβ) and T-cell receptor gene rearrangement (TCR-GR) analyses for differentiating T-cell large granular lymphocytic leukemia (T-LGLL) from reactive T-large granular lymphocyte (T-LGL) lymphocytosis has been insufficiently studied to date. In this study, we analyzed the diagnostic value of TCR-GR and FC-Vβ analysis in T-LGLL, and compared these results. In our study, FC-Vβ analysis was positive in all cases of T-LGLL, and clonality assessment of FC-Vβ had equal sensitivity and specificity to GeneScanning analysis but was more sensitive than heteroduplex analysis. Suspected T-cell clonality can best be addressed by evaluating two TCR targets (TCRβ and TCRγ), either in parallel or consecutively. Signal transducer and activator of transcription 3 (STAT3) mutation may provide a diagnostic tool for classifying some cases of T-LGL lymphocytosis as true T-LGLL. Our results further demonstrate a significant correlation of STAT3 mutation with pure red cell aplasia, neutropenia, hepatomegaly, β2-microglobulin and anemia.
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Authors | Zhi-Yuan Qiu, Wen-Yi Shen, Lei Fan, Li Wang, Hui Yu, Chun Qiao, Yu-Jie Wu, Rui-Nan Lu, Jun Qian, Guang-Sheng He, Wei Xu, Jian-Yong Li |
Journal | Leukemia & lymphoma
(Leuk Lymphoma)
Vol. 56
Issue 2
Pg. 324-31
(Feb 2015)
ISSN: 1029-2403 [Electronic] United States |
PMID | 24828862
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Receptors, Antigen, T-Cell
- STAT3 Transcription Factor
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Topics |
- Aged
- Clone Cells
(metabolism, pathology)
- Diagnosis, Differential
- Female
- Flow Cytometry
(methods)
- Gene Rearrangement
- Humans
- Leukemia, Large Granular Lymphocytic
(diagnosis, genetics)
- Lymphocytosis
(diagnosis, genetics)
- Male
- Middle Aged
- Mutation
- Receptors, Antigen, T-Cell
(genetics)
- STAT3 Transcription Factor
(genetics)
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