Stromal-derived factor-1 abolishes constitutive apoptosis of WHIM syndrome neutrophils harbouring a truncating CXCR4 mutation

Br J Haematol. 2006 Sep;134(6):640-4. doi: 10.1111/j.1365-2141.2006.06240.x. Epub 2006 Aug 9.

Abstract

Warts, hypogammaglobulinaemia, infections, myelokathexis (WHIM) syndrome is an inherited immune disorder associated with CXCR4 gene mutations. Recent studies suggested that impaired receptor downregulation and enhanced chemotactic responsiveness to stromal-derived factor-1 (SDF-1), the sole cognate ligand for CXCR4, may account for the characteristic features of WHIM patients. This study evaluated whether the interaction of SDF-1 with CXCR4 could block constitutive apoptosis of peripheral blood neutrophils from congenital neutropenia patients and controls. SDF-1 was found to be a potent anti-apoptotic factor for WHIM neutrophils harbouring a truncating CXCR4 mutation, but not for neutrophils from control individuals, thus supporting the notion that such mutations may confer enhanced functional responses.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Agammaglobulinemia / immunology*
  • Agammaglobulinemia / pathology
  • Apoptosis / drug effects
  • Case-Control Studies
  • Cell Culture Techniques
  • Chemokine CXCL12
  • Chemokines, CXC / pharmacology*
  • Female
  • Humans
  • Immunologic Deficiency Syndromes / immunology*
  • Immunologic Deficiency Syndromes / pathology
  • Infections / immunology
  • Infections / pathology
  • Mutation
  • Neutrophils / metabolism
  • Neutrophils / pathology*
  • Receptors, CXCR4 / genetics*
  • Receptors, CXCR4 / metabolism
  • Syndrome
  • Warts / immunology*
  • Warts / pathology

Substances

  • CXCL12 protein, human
  • Chemokine CXCL12
  • Chemokines, CXC
  • Receptors, CXCR4