Literature DB >> 26981933

Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

H S Kuehn1, B Boisson1, M E Conley1, S D Rosenzweig1, C Cunningham-Rundles1, J Reichenbach1, A Stray-Pedersen1, E W Gelfand1, P Maffucci1, K R Pierce1, J K Abbott1, K V Voelkerding1, S T South1, N H Augustine1, J S Bush1, W K Dolen1, B B Wray1, Y Itan1, A Cobat1, H S Sorte1, S Ganesan1, S Prader1, T B Martins1, M G Lawrence1, J S Orange1, K R Calvo1, J E Niemela1, J-L Casanova1, T A Fleisher1, H R Hill1, A Kumánovics1.   

Abstract

BACKGROUND: Common variable immunodeficiency (CVID) is characterized by late-onset hypogammaglobulinemia in the absence of predisposing factors. The genetic cause is unknown in the majority of cases, and less than 10% of patients have a family history of the disease. Most patients have normal numbers of B cells but lack plasma cells.
METHODS: We used whole-exome sequencing and array-based comparative genomic hybridization to evaluate a subset of patients with CVID and low B-cell numbers. Mutant proteins were analyzed for DNA binding with the use of an electrophoretic mobility-shift assay (EMSA) and confocal microscopy. Flow cytometry was used to analyze peripheral-blood lymphocytes and bone marrow aspirates.
RESULTS: Six different heterozygous mutations in IKZF1, the gene encoding the transcription factor IKAROS, were identified in 29 persons from six families. In two families, the mutation was a de novo event in the proband. All the mutations, four amino acid substitutions, an intragenic deletion, and a 4.7-Mb multigene deletion involved the DNA-binding domain of IKAROS. The proteins bearing missense mutations failed to bind target DNA sequences on EMSA and confocal microscopy; however, they did not inhibit the binding of wild-type IKAROS. Studies in family members showed progressive loss of B cells and serum immunoglobulins. Bone marrow aspirates in two patients had markedly decreased early B-cell precursors, but plasma cells were present. Acute lymphoblastic leukemia developed in 2 of the 29 patients.
CONCLUSIONS: Heterozygous mutations in the transcription factor IKAROS caused an autosomal dominant form of CVID that is associated with a striking decrease in B-cell numbers. (Funded by the National Institutes of Health and others.).

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Year:  2016        PMID: 26981933      PMCID: PMC4836293          DOI: 10.1056/NEJMoa1512234

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  41 in total

1.  Ikaros, an early lymphoid-specific transcription factor and a putative mediator for T cell commitment.

Authors:  K Georgopoulos; D D Moore; B Derfler
Journal:  Science       Date:  1992-10-30       Impact factor: 47.728

2.  Ikaros sets thresholds for T cell activation and regulates chromosome propagation.

Authors:  N Avitahl; S Winandy; C Friedrich; B Jones; Y Ge; K Georgopoulos
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3.  Human Ikaros function in activated T cells is regulated by coordinated expression of its largest isoforms.

Authors:  Tapani Ronni; Kimberly J Payne; Sam Ho; Michelle N Bradley; Glenn Dorsam; Sinisa Dovat
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4.  LyF-1, a transcriptional regulator that interacts with a novel class of promoters for lymphocyte-specific genes.

Authors:  K Lo; N R Landau; S T Smale
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

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Authors:  Carrie L Lucas; Hye Sun Kuehn; Fang Zhao; Julie E Niemela; Elissa K Deenick; Umaimainthan Palendira; Danielle T Avery; Leen Moens; Jennifer L Cannons; Matthew Biancalana; Jennifer Stoddard; Weiming Ouyang; David M Frucht; V Koneti Rao; T Prescott Atkinson; Anahita Agharahimi; Ashleigh A Hussey; Les R Folio; Kenneth N Olivier; Thomas A Fleisher; Stefania Pittaluga; Steven M Holland; Jeffrey I Cohen; Joao B Oliveira; Stuart G Tangye; Pamela L Schwartzberg; Michael J Lenardo; Gulbu Uzel
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