CTLA-4 +49A>G polymorphism of recipients of HLA-matched sibling allogeneic stem cell transplantation is associated with survival and relapse incidence

Ann Hematol. 2010 Jun;89(6):613-8. doi: 10.1007/s00277-009-0885-5. Epub 2009 Dec 18.

Abstract

Conflicting observations have been reported about the role of CTLA-4 gene polymorphisms in the clinical outcome of allogeneic hematopoietic stem cell transplantation (HSCT). We have investigated three polymorphisms of the CTLA-4 gene (-318C>T, +49A>G, CT60G>A) in 133 donor/recipient pairs who underwent HLA-matched sibling donor HSCT for hematological malignancies. We found no association of the clinical outcome of the HSCT with either recipient or donor -318C>T and CT60G>A polymorphisms. At variance, we found a significant association of donor +49A>G G/G genotype with longer overall survival (OS; log-rank test, P = 0.04), and the number of +49A>G G-alleles in the recipient with longer OS (P = 0.027), longer disease-free survival (P = 0.036) and reduced relapse rate (P = 0.042). However, only recipient +49A>G polymorphism was retained as independent prognostic factor in a multivariate analysis, suggesting that the expression of CTLA-4 on the cells of recipient may be relevant for the clinical outcome of HSCT.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antigens, CD / genetics*
  • CTLA-4 Antigen
  • Female
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Hematopoietic Stem Cell Transplantation / statistics & numerical data
  • Histocompatibility Testing
  • Humans
  • Male
  • Middle Aged
  • Myelodysplastic-Myeloproliferative Diseases / epidemiology
  • Myelodysplastic-Myeloproliferative Diseases / genetics
  • Myelodysplastic-Myeloproliferative Diseases / mortality*
  • Myelodysplastic-Myeloproliferative Diseases / therapy*
  • Polymorphism, Single Nucleotide* / physiology
  • Recurrence
  • Retrospective Studies
  • Siblings*
  • Survival Analysis
  • Transplantation, Homologous
  • Young Adult

Substances

  • Antigens, CD
  • CTLA-4 Antigen
  • CTLA4 protein, human