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Neutrophil Elastase Defects in Congenital Neutropenia.

Authors :
Rydzynska Z
Pawlik B
Krzyzanowski D
Mlynarski W
Madzio J
Source :
Frontiers in immunology [Front Immunol] 2021 Apr 22; Vol. 12, pp. 653932. Date of Electronic Publication: 2021 Apr 22 (Print Publication: 2021).
Publication Year :
2021

Abstract

Severe congenital neutropenia (SCN) is a rare hematological condition with heterogenous genetic background. Neutrophil elastase (NE) encoded by ELANE gene is mutated in over half of the SCN cases. The role of NE defects in myelocytes maturation arrest in bone marrow is widely investigated; however, the mechanism underlying this phenomenon has still remained unclear. In this review, we sum up the studies exploring mechanisms of neutrophil deficiency, biological role of NE in neutrophil and the effects of ELANE mutation and neutropenia pathogenesis. We also explain the hypotheses presented so far and summarize options of neutropenia therapy.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Rydzynska, Pawlik, Krzyzanowski, Mlynarski and Madzio.)

Details

Language :
English
ISSN :
1664-3224
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
33968054
Full Text :
https://doi.org/10.3389/fimmu.2021.653932