Hematopoietic Processes in Eosinophilic Asthma

Chest. 2017 Aug;152(2):410-416. doi: 10.1016/j.chest.2017.01.021. Epub 2017 Jan 24.

Abstract

Airway eosinophilia is a hallmark of allergic asthma, and understanding mechanisms that promote increases in lung eosinophil numbers is important for effective pharmacotherapeutic development. It has become evident that expansion of hematopoietic compartments in the bone marrow (BM) promotes differentiation and trafficking of mature eosinophils to the airways. Hematopoietic progenitor cells egress the BM and home to the lungs, where in situ differentiation within the tissue provides an ongoing source of proinflammatory cells. In addition, hematopoietic progenitor cells in the airways can respond to locally derived alarmins to produce a panoply of cytokines, thereby themselves acting as effector proinflammatory cells that potentiate type 2 responses in eosinophilic asthma. In this review, we provide evidence for these findings and discuss novel targets for modulating eosinophilopoietic processes, migration, and effector function of precursor cells.

Keywords: airway inflammation; allergic asthma; asthma; bone marrow.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Asthma / drug therapy
  • Asthma / etiology*
  • Asthma / physiopathology
  • CD4-Positive T-Lymphocytes / physiology
  • Cell Differentiation / physiology
  • Cytokine Receptor Common beta Subunit / antagonists & inhibitors
  • Cytokines / antagonists & inhibitors
  • Cytokines / physiology
  • Eosinophils / cytology
  • Eosinophils / physiology
  • Hematopoiesis / physiology*
  • Hematopoietic Stem Cells / physiology
  • Humans
  • Membrane Proteins / antagonists & inhibitors
  • Pulmonary Eosinophilia / drug therapy
  • Pulmonary Eosinophilia / etiology*
  • Pulmonary Eosinophilia / physiopathology
  • Respiratory Hypersensitivity / etiology
  • Respiratory Hypersensitivity / physiopathology
  • Thymic Stromal Lymphopoietin

Substances

  • Antibodies, Monoclonal, Humanized
  • Cytokine Receptor Common beta Subunit
  • Cytokines
  • Membrane Proteins
  • TMEM102 protein, human
  • Thymic Stromal Lymphopoietin