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Neutrophil Elastase Defects in Congenital Neutropenia.
- 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.)
- Subjects :
- Gene Expression Regulation
Humans
Leukocyte Elastase chemistry
Leukocyte Elastase genetics
Leukocyte Elastase metabolism
Mutation
Neutropenia diagnosis
Neutropenia genetics
Protein Processing, Post-Translational
Protein Transport
Signal Transduction
Structure-Activity Relationship
Congenital Bone Marrow Failure Syndromes diagnosis
Congenital Bone Marrow Failure Syndromes genetics
Genetic Association Studies
Genetic Predisposition to Disease
Leukocyte Elastase deficiency
Neutropenia congenital
Neutrophils enzymology
Subjects
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