血管免疫母细胞性T细胞淋巴瘤
淋巴瘤
造血
IDH2型
克隆(Java方法)
多克隆B细胞反应
生物
分子生物学
癌症研究
IGHV@
人口
突变
B细胞
遗传学
免疫学
白血病
基因
干细胞
医学
T细胞
抗体
慢性淋巴细胞白血病
B细胞受体
IDH1
环境卫生
免疫系统
作者
Friederike H. Schwartz,Qian Cai,Eva Fellmann,Sylvia Hartmann,Mikko I. Mäyränpää,Marja‐Liisa Karjalainen‐Lindsberg,Christer Sundström,René Scholtysik,Martin‐Leo Hansmann,Ralf Küppers
摘要
Angioimmunoblastic T-cell lymphomas (AITLs) frequently carry mutations in the TET2 and IDH2 genes. TET2 mutations represent early genetic lesions as they had already been detected in haematopoietic precursor cells of AITL patients. We show by analysis of whole-tissue sections and microdissected PD1+ cells that the frequency of TET2-mutated AITL is presumably even higher than reported (12/13 cases in our collection; 92%). In two-thirds of informative AITLs (6/9), a fraction of B cells was also TET2-mutated. Investigation of four AITLs by TET2 and IGHV gene sequencing of single microdissected B cells showed that between 10% and 60% of polyclonal B cells in AITL lymph nodes harboured the identical TET2 mutations of the respective T-cell lymphoma clone. Thus, TET2-mutated haematopoietic precursor cells in AITL patients not only give rise to the T-cell lymphoma but also generate a large population of mutated mature B cells. Future studies will show whether this is a reason why AITL patients frequently also develop B-cell lymphomas. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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