Hyperinflammation in patients with chronic granulomatous disease leads to impairment of hematopoietic stem cell functions

J Allergy Clin Immunol. 2016 Jul;138(1):219-228.e9. doi: 10.1016/j.jaci.2015.11.028. Epub 2016 Feb 4.

Abstract

Background: Defects in phagocytic nicotinamide adenine dinucleotide phosphate oxidase 2 (NOX2) function cause chronic granulomatous disease (CGD), a primary immunodeficiency characterized by dysfunctional microbicidal activity and chronic inflammation.

Objective: We sought to study the effect of chronic inflammation on the hematopoietic compartment in patients and mice with X-linked chronic granulomatous disease (X-CGD).

Methods: We used immunostaining and functional analyses to study the hematopoietic compartment in patients with CGD.

Results: An analysis of bone marrow cells from patients and mice with X-CGD revealed a dysregulated hematopoiesis characterized by increased numbers of hematopoietic progenitor cells (HPCs) at the expense of repopulating hematopoietic stem cells (HSCs). In patients with X-CGD, there was a clear reduction in the proportion of HSCs in bone marrow and peripheral blood, and they were also more rapidly exhausted after in vitro culture. In mice with X-CGD, increased cycling of HSCs, expansion of HPCs, and impaired long-term engraftment capacity were found to be associated with high concentrations of proinflammatory cytokines, including IL-1β. Treatment of wild-type mice with IL-1β induced enhanced cell-cycle entry of HSCs, expansion of HPCs, and defects in long-term engraftment, mimicking the effects observed in mice with X-CGD. Inhibition of cytokine signaling in mice with X-CGD reduced HPC numbers but had only minor effects on the repopulating ability of HSCs.

Conclusions: Persistent chronic inflammation in patients with CGD is associated with hematopoietic proliferative stress, leading to a decrease in the functional activity of HSCs. Our observations have clinical implications for the development of successful autologous cell therapy approaches.

Keywords: Chronic granulomatous disease; IL-1β; anakinra; cell cycle; competitive repopulation assay; dysfunctional hematopoiesis; engraftment defect; gene therapy; hematopoietic stem cell; hyperinflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Biomarkers
  • Case-Control Studies
  • Cell Count
  • Cell Differentiation
  • Child
  • Child, Preschool
  • Colony-Forming Units Assay
  • Cytokines / metabolism
  • Cytokines / pharmacology
  • Disease Models, Animal
  • Graft Survival
  • Granulomatous Disease, Chronic / etiology
  • Granulomatous Disease, Chronic / metabolism*
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism*
  • Humans
  • Immunophenotyping
  • Inflammation Mediators / metabolism
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Phenotype
  • Signal Transduction
  • Young Adult

Substances

  • Biomarkers
  • Cytokines
  • Inflammation Mediators