Genetic variant of the G-CSF receptor gene is associated with lower mobilization potential and slower recovery of granulocytes after transplantation of autologous peripheral blood progenitor cells

Cytokine. 2012 Nov;60(2):463-7. doi: 10.1016/j.cyto.2012.06.021. Epub 2012 Jul 15.

Abstract

Peripheral blood mobilized by cytokines (i.e. granulocyte colony stimulating factor, G-CSF) and chemotherapy has become a major source of hematopoietic stem and progenitor cells for transplantation (PBPCT). In this study the effect of the G-CSF receptor (CSF3R) gene polymorphism was investigated. The presence of the CSF3R variant (T allele, rs3917924) was related to CD34(+) mobilization yield and the pace of granulocyte recovery after autologous PBPCT. The mobilization yield was higher in patients lacking the CSF3R variant (OR=4.756, p=0.046) and those with multiple myeloma (OR=10.534, p=0.019). The pace of granulocyte recovery was found to be associated with the CSF3R polymorphism and was significantly slower in patients carrying the CSF3R-T variant than in CC homozygotes (median of 17 vs. 13 days, p<0.001). This association was confirmed (OR=4.445, p=0.014) by multiple regression analysis considering patient age and sex, the number of transplanted CD34(+) cells, diagnosis and CSF3R polymorphism. These results imply that CSF3R gene polymorphism plays a significant role in PBPCT.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Antigens, CD34 / metabolism
  • Cell Count
  • Female
  • Genetic Association Studies*
  • Genotype
  • Granulocytes / metabolism*
  • Hematopoietic Stem Cell Mobilization*
  • Humans
  • Male
  • Middle Aged
  • Peripheral Blood Stem Cell Transplantation*
  • Polymorphism, Single Nucleotide / genetics*
  • Receptors, Colony-Stimulating Factor / genetics*
  • Regression Analysis
  • Transplantation, Autologous
  • Young Adult

Substances

  • Antigens, CD34
  • CSF3R protein, human
  • Receptors, Colony-Stimulating Factor