The role of danger signals and ectonucleotidases in acute graft-versus-host disease

Hum Immunol. 2016 Nov;77(11):1037-1047. doi: 10.1016/j.humimm.2016.02.005. Epub 2016 Feb 20.

Abstract

Allogeneic hematopoietic cell transplantation (allo-HCT) represents the only curative treatment approach for many patients with benign or malignant diseases of the hematopoietic system. However, post-transplant morbidity and mortality are significantly increased by the development of acute graft-versus-host disease (GvHD). While alloreactive T cells act as the main cellular mediator of the GvH reaction, recent evidence suggests a critical role of the innate immune system in the early stages of GvHD initiation. Danger-associated molecular patterns released from the intracellular space as well as from the extracellular matrix activate antigen-presenting cells and set pro-inflammatory pathways in motion. This review gives an overview about danger signals representing therapeutic targets with a clinical perspective with a particular focus on extracellular nucleotides and ectonucleotidases.

Keywords: ATP; Adenosine; Allogeneic hematopoietic cell transplantation; DAMP; Ectonucleotidase; Graft-versus-host disease; HMGB1; Heat shock protein; Inflammasome; S100 protein family; Uric acid.

Publication types

  • Review

MeSH terms

  • Acute Disease
  • Animals
  • Antigens, CD / metabolism*
  • Apyrase / metabolism*
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / immunology*
  • Hematologic Neoplasms / complications
  • Hematologic Neoplasms / therapy*
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immunity, Innate
  • Pyrophosphatases / metabolism*
  • Receptors, Pattern Recognition / metabolism
  • T-Lymphocytes / immunology*
  • Transplantation, Homologous

Substances

  • Antigens, CD
  • Receptors, Pattern Recognition
  • Pyrophosphatases
  • Apyrase
  • CD39 antigen