Literature DB >> 28337768

TET2 mutations in B cells of patients affected by angioimmunoblastic T-cell lymphoma.

Friederike H Schwartz1,2, Qian Cai1, Eva Fellmann2, Sylvia Hartmann2, Mikko I Mäyränpää3,4, Marja-Liisa Karjalainen-Lindsberg3,4, Christer Sundström5, René Scholtysik1, Martin-Leo Hansmann2,6, Ralf Küppers1,6.   

Abstract

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. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Entities:  

Keywords:  B cells; IDH2; TET2; angioimmunoblastic T-cell lymphoma; somatic mutation

Mesh:

Substances:

Year:  2017        PMID: 28337768     DOI: 10.1002/path.4898

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   9.883


  20 in total

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