细胞仪
CD19
骨髓
CD38
医学
慢性淋巴细胞白血病
CD5型
CD20
B细胞
免疫系统
抗原
抗体
病理
作者
Valentina Giudice,Matteo D'Addona,Nunzia Montuori,Carmine Selleri
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2021-09-08
卷期号:13 (18): 4513-4513
被引量:2
标识
DOI:10.3390/cancers13184513
摘要
Large granular lymphocyte (LGL) leukemia is a lymphoproliferative disorder of mature T or NK cells frequently associated with autoimmune disorders and other hematological conditions, such as myelodysplastic syndromes. Immunophenotype of LGL cells is similar to that of effector memory CD8+ T cells with T-cell receptor (TCR) clonality defined by molecular and/or flow cytometric analysis. Vβ usage by flow cytometry can identify clonal TCR rearrangements at the protein level, and is fast, sensitive, and almost always available in every Hematology Center. Moreover, Vβ usage can be associated with immunophenotypic characterization of LGL clone in a multiparametric staining, and clonal kinetics can be easily monitored during treatment and follow-up. Finally, Vβ usage by flow cytometry might identify LGL clones silently underlying other hematological conditions, and routine characterization of Vβ skewing might identify recurrent TCR rearrangements that might trigger aberrant immune responses during hematological or autoimmune conditions.
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