Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.
Postgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
Front Immunol. 2021 Apr 22;12:653932. doi: 10.3389/fimmu.2021.653932. eCollection 2021.
Severe congenital neutropenia (SCN) is a rare hematological condition with heterogenous genetic background. Neutrophil elastase (NE) encoded by 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 mutation and neutropenia pathogenesis. We also explain the hypotheses presented so far and summarize options of neutropenia therapy.
严重先天性中性粒细胞减少症(SCN)是一种罕见的血液学疾病,具有异质性的遗传背景。超过一半的 SCN 病例中,基因编码的中性粒细胞弹性蛋白酶(NE)发生突变。NE 缺陷导致骨髓中髓细胞成熟停滞的作用已得到广泛研究;然而,这一现象的机制仍不清楚。在这篇综述中,我们总结了探索中性粒细胞缺乏机制、NE 在中性粒细胞中的生物学作用以及突变和中性粒细胞减少症发病机制的研究。我们还解释了迄今为止提出的假说,并总结了中性粒细胞减少症的治疗选择。