Mutations in the neutrophil elastase gene in cyclic and congenital neutropenia

Curr Opin Immunol. 2001 Oct;13(5):535-8. doi: 10.1016/s0952-7915(00)00254-5.

Abstract

Severe neutropenia disorders are characterized by extremely low levels of peripheral blood neutrophils, a maturation block of bone marrow progenitor cells and recurring severe bacterial and fungal infections. Recent reports indicated that severe neutropenia is a consequence of an impaired survival and abnormal cell cycle progression of myeloid progenitor cells in both cyclic and severe congenital neutropenia. Mutations in the neutrophil elastase gene were identified in all patients with cyclic neutropenia and most of the patients with severe congenital neutropenia. We hypothesize that expression of mutant neutrophil elastase protein results in deregulation of intracellular activity and premature cell death of myeloid-committed progenitor cells in these disorders, resulting in the lack of peripheral blood neutrophils. The potential molecular mechanisms of mutant-protein-mediated neutropenia is discussed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Humans
  • Leukocyte Elastase / genetics*
  • Mutation / genetics*
  • Neutropenia / congenital*
  • Neutropenia / enzymology*
  • Neutropenia / genetics
  • Periodicity*

Substances

  • Leukocyte Elastase