Induction of a hypercoagulability state and endothelial cell activation by granulocyte colony-stimulating factor in peripheral blood stem cell donors

J Hematother Stem Cell Res. 2002 Aug;11(4):675-81. doi: 10.1089/15258160260194820.

Abstract

In June, 1997, we initiated a prospective study to analyze the effect of granulocyte colony-stimulating factor (G-CSF) on coagulation system in peripheral blood stem cells (PBSC) donors following G-CSF administration. Since, 25 consecutively healthy donors received G-CSF (filgrastim) to mobilize and collect PBSC and 20 donors were finally included in the study. Blood samples were collected immediately before starting G-CSF and prior to PBSC collection to analyze the following parameters: prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen, hypercoagulability markers (D-dimer, TAT complex, F1 + 2), natural anticoagulants (antithrombin, protein C, protein S), endothelial activation markers [von Willebrand factor antigen (vWF:Ag) and angiotensin converting enzyme (ACE)], and resistance to activated protein C. We found a significant increase in F1 + 2 and D-dimer while a significant decrease of antithrombin and protein C activity was evidenced. Regarding endothelial cell activation markers, a significant increase of vWF:Ag with a slightly significant decrease of ACE were also observed. Therefore, in PBSC donors receiving G-CSF our results reveal activation of both coagulation and endothelial cells that could favor the developing of thrombotic events. In consequence, a careful monitoring should be considered in those cases with risk factors for thrombosis.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Blood Coagulation
  • Blood Component Removal / methods
  • Endothelium, Vascular / physiopathology*
  • Female
  • Filgrastim
  • Granulocyte Colony-Stimulating Factor / therapeutic use*
  • Hematopoietic Stem Cell Mobilization / methods*
  • Histocompatibility Testing
  • Humans
  • Male
  • Middle Aged
  • Partial Thromboplastin Time
  • Prospective Studies
  • Prothrombin Time
  • Recombinant Proteins
  • Thrombophilia / blood
  • Thrombophilia / physiopathology*
  • Tissue Donors*
  • von Willebrand Factor / analysis

Substances

  • Recombinant Proteins
  • von Willebrand Factor
  • Granulocyte Colony-Stimulating Factor
  • Filgrastim