Peripheral microchimerism in long-term cadaveric-kidney allograft recipients

Lancet. 1994 Jun 11;343(8911):1468-9. doi: 10.1016/s0140-6736(94)92583-6.

Abstract

Microchimerism after allogeneic organ transplantation may be a mechanism for induction of donor-specific graft acceptance. However, the frequency of chimerism and its relevance in long-term tolerance are uncertain. We studied 15 long-surviving (more than 20 years) cadaveric-kidney transplant recipients for the systemic presence of donor alleles with allele-specific genomic amplification of DRB1 and H-Y loci. Microchimerism was observed in 1 case in peripheral blood and in 4 cases in skin. Chimerism and number of HLA alleles shared by donor and recipient were not correlated. This low frequency of microchimerism in long-term kidney allograft recipients raises doubts about a major participation of chimerism in donor-specific tolerance.

MeSH terms

  • Blood Grouping and Crossmatching
  • DNA / analysis
  • Female
  • Follow-Up Studies
  • Gene Amplification
  • Genotype
  • Graft Survival / immunology*
  • HLA Antigens / genetics
  • Humans
  • Immune Tolerance / genetics
  • Kidney Transplantation / immunology*
  • Male
  • Transplantation Chimera / genetics*
  • Transplantation, Homologous

Substances

  • HLA Antigens
  • DNA