Literature DB >> 19415009

Ela2 mutations and clinical manifestations in familial congenital neutropenia.

Masaaki Shiohara1, Tomonari Shigemura, Shoji Saito, Miyuki Tanaka, Ryu Yanagisawa, Kazuo Sakashita, Hiroshi Asada, Eizaburo Ishii, Kazutoshi Koike, Motoaki Chin, Masao Kobayashi, Kenichi Koike.   

Abstract

PURPOSE: Three familial cases of each of severe congenital neutropenia (SCN) and cyclic neutropenia (CN) in addition to 3 sporadic cases of SCN were analyzed for neutrophil elastase (Ela2) gene mutation. The contents of the neutrophil-specific granule proteins cathelicidin antimicrobial peptide and neutrophil gelatinase-associated lipocalin were also analyzed in SCN.
METHODS: Genomic DNA was extracted from the patients' peripheral blood or bone marrow, and the coding sequence of the Ela2 gene was amplified by polymerase chain reaction and subjected to direct sequencing. The contents of antimicrobial peptides were analyzed by flow cytometry.
RESULTS: Three cases of familial SCN (P13L, R52P, and S97L), 2 of familial CN (W212stop and P110L), and 1 of sporadic SCN (V72M) were shown to have heterozygous mutations in the Ela2 gene. W212stop found in a familial CN case was a novel mutation of Ela2. Prophylactic treatment for growth factors or antibiotic prophylaxis against bacterial infection was useful for lowering the frequency of infectious episodes. Adult patients tended to have less frequent infections compared with minors in the same family. The contents of both cathelicidin antimicrobial peptide and neutrophil gelatinase-associated lipocalin were significantly reduced in SCN compared with healthy controls.
CONCLUSIONS: Prophylaxis by growth factor or antibiotics is useful for decreasing risks of bacterial infections in SCN and CN. Adults were likely to have less frequent infections than children in familial cases of SCN and CN with the same mutation of Ela2.

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Year:  2009        PMID: 19415009     DOI: 10.1097/MPH.0b013e3181984dbe

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  5 in total

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Journal:  Am J Hum Genet       Date:  2016-08-04       Impact factor: 11.025

2.  Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation.

Authors:  Esther van de Vosse; Els M Verhard; Anton J T Tool; Adriëtte W de Visser; Taco W Kuijpers; Pieter S Hiemstra; Jaap T van Dissel
Journal:  Ann Hematol       Date:  2010-08-28       Impact factor: 3.673

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Journal:  Int J Mol Sci       Date:  2020-06-30       Impact factor: 5.923

Review 4.  The genetics of human hematopoiesis and its disruption in disease.

Authors:  Erik L Bao; Aaron N Cheng; Vijay G Sankaran
Journal:  EMBO Mol Med       Date:  2019-07-17       Impact factor: 12.137

Review 5.  Assessment of Congenital Neutropenia in Children: Common Clinical Sceneries and Clues for Management.

Authors:  Ilaria Lazzareschi; Elena Rossi; Antonietta Curatola; Giovanna Capozio; Luca Benacquista; Ludovica Iezzi; Donato Rigante
Journal:  Mediterr J Hematol Infect Dis       Date:  2022-01-01       Impact factor: 2.576

  5 in total

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