Distribution of the minor histocompatibility antigens in Korean population and disparities in unrelated hematopoietic SCT

Bone Marrow Transplant. 2007 Oct;40(8):723-8. doi: 10.1038/sj.bmt.1705808. Epub 2007 Aug 13.

Abstract

Minor histocompatibility antigens (mHags) are polymorphic peptides presented to T lymphocytes restricted by the MHC molecule. It has been reported that disparities of mHags are a potential risk factor for GVHD after hematopoietic SCT (HSCT). Here we observed allelic frequencies of HA-1, -2 and -8 in 139 Korean healthy individuals using PCR-sequence-specific primers, and analyzed the correlation between disparity of these mHags and acute GVHD (aGVHD) in 54 patients who underwent HSCT from unrelated HLA-identical donors. The allelic frequencies in Korean healthy individuals were 39.6 and 60.4% for HA-1(H) and HA-1(R), 92.4 and 7.6% for HA-2(M) and HA-2(V), 36.7 and 63.3% for HA-8(R) and HA-8(P), respectively. The frequencies of mHags incompatibility known to be associated with aGVHD were 16.7% in HA-1, 0% in HA-2 and 25.9% in HA-8. However, the statistically significant association of aGVHD with these mHags incompatibility was not found between healthy donors and leukemia patients after unrelated HSCT. This first report about mHags in Koreans may be helpful in further defining the clinical impact of mHags disparities in HSCT and in comparing with other populations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Gene Frequency
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / immunology*
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Infant
  • Korea / epidemiology
  • Leukemia / immunology
  • Male
  • Middle Aged
  • Minor Histocompatibility Antigens / genetics*
  • Neoplasm Proteins / genetics
  • Oligopeptides / genetics
  • Tissue Donors / statistics & numerical data

Substances

  • HA-1 antigen
  • HA-2 antigen
  • Minor Histocompatibility Antigens
  • Neoplasm Proteins
  • Oligopeptides
  • PUM3 protein, human